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You searched for subject:(High Throughput Nucleotide Sequencing). Showing records 1 – 30 of 36961 total matches.

[1] [2] [3] [4] [5] … [1233]

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University of Texas Southwestern Medical Center

1. Porter, Shaina N. 1983-. Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution.

Degree: 2012, University of Texas Southwestern Medical Center

 It is increasingly recognized that tracking the clonal dynamics of large populations is important in understanding aspects of cancer and stem cell biology. Attempts to… (more)

Subjects/Keywords: Clonal Evolution; DNA Barcoding, Taxonomic; High-Throughput Nucleotide Sequencing

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Porter, S. N. 1. (2012). Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-54

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Porter, Shaina N 1983-. “Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-54.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Porter, Shaina N 1983-. “Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution.” 2012. Web. 05 Dec 2020.

Vancouver:

Porter SN1. Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-54.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Porter SN1. Illuminating Clonal Dynamics: Development and Use of a High-Throughput Cellular Barcoding System to Track Clonal Evolution. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-54

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Sheppard, Sarah E. Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation.

Degree: PhD, Molecular, Cell and Cancer Biology Department, 2013, U of Massachusetts : Med

  Cleavage and polyadenylation of a precursor mRNA is important for transcription termination, mRNA stability, and regulation of gene expression. This process is directed by… (more)

Subjects/Keywords: Bayes Theorem; Algorithms; Polyadenylation; RNA 3' Polyadenylation Signals; High-Throughput Nucleotide Sequencing; Bioinformatics; Computational Biology

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APA (6th Edition):

Sheppard, S. E. (2013). Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/653

Chicago Manual of Style (16th Edition):

Sheppard, Sarah E. “Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/653.

MLA Handbook (7th Edition):

Sheppard, Sarah E. “Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation.” 2013. Web. 05 Dec 2020.

Vancouver:

Sheppard SE. Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/653.

Council of Science Editors:

Sheppard SE. Application of a Naïve Bayes Classifier to Assign Polyadenylation Sites from 3' End Deep Sequencing Data: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/653


University of Texas Southwestern Medical Center

3. Rounds, William Harold Alexander. Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients.

Degree: 2016, University of Texas Southwestern Medical Center

 Multiple sclerosis (MS) diagnosis primarily revolves around the use of brain lesion detection by MRI and the elimination of other possible neurological disorder diagnoses through… (more)

Subjects/Keywords: B-Lymphocytes; Genes, Immunoglobulin; High-Throughput Nucleotide Sequencing; Multiple Sclerosis; Sequence Analysis, DNA

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APA (6th Edition):

Rounds, W. H. A. (2016). Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5747

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rounds, William Harold Alexander. “Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/5747.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rounds, William Harold Alexander. “Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients.” 2016. Web. 05 Dec 2020.

Vancouver:

Rounds WHA. Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/5747.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rounds WHA. Clinical Diagnostic Potential and Characterization of Distinctly Hypermutated Antibodies in Multiple Sclerosis Patients. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5747

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

4. Wang, Tao. Understanding RNA Regulation Through Analysis of CLIP-Seq Data.

Degree: 2015, University of Texas Southwestern Medical Center

 The past decades have witnessed a surge of discoveries revealing RNA regulation as a central player in cellular processes. The advent of cross-linking immunoprecipitation coupled… (more)

Subjects/Keywords: Genomics; High-Throughput Nucleotide Sequencing; RNA; RNA-Binding Proteins; Sequence Analysis, RNA

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wang, T. (2015). Understanding RNA Regulation Through Analysis of CLIP-Seq Data. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4457

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wang, Tao. “Understanding RNA Regulation Through Analysis of CLIP-Seq Data.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/4457.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wang, Tao. “Understanding RNA Regulation Through Analysis of CLIP-Seq Data.” 2015. Web. 05 Dec 2020.

Vancouver:

Wang T. Understanding RNA Regulation Through Analysis of CLIP-Seq Data. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/4457.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang T. Understanding RNA Regulation Through Analysis of CLIP-Seq Data. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4457

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

5. Tsuneda, Simone Sayuri, 1974-. Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias.

Degree: 2012, Universidade Estadual de Campinas

 Abstract: Polimicrogyria (PMG) is a cortical malformation caused by failures during the brain cortex development process and is characterized by an excessive number of small… (more)

Subjects/Keywords: Epilepsia; Genes; Malformações do desenvolvimento cortical; Sequência de nucleotídeos; Epilepsy; Genes; Malformations of cortical development; Nucleotide sequence; High-throughput nucleotide sequencing

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APA (6th Edition):

Tsuneda, Simone Sayuri, 1. (2012). Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/309734

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tsuneda, Simone Sayuri, 1974-. “Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias.” 2012. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/309734.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tsuneda, Simone Sayuri, 1974-. “Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias.” 2012. Web. 05 Dec 2020.

Vancouver:

Tsuneda, Simone Sayuri 1. Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias. [Internet] [Thesis]. Universidade Estadual de Campinas; 2012. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/309734.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tsuneda, Simone Sayuri 1. Estratégia para investigação molecular de epilepsia com identificação de genes relacionados a formas de polimicrogiria = Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias: Strategy of molecular investigation on epilepsy with the identification of genes related to poymicrogyrias. [Thesis]. Universidade Estadual de Campinas; 2012. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/309734

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Georgia Tech

6. Jammula, Nagakishore. Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets.

Degree: PhD, Electrical and Computer Engineering, 2019, Georgia Tech

 The objective of this research is to develop parallel algorithms for enabling fast and scalable analysis of large-scale high-throughput sequencing datasets. Genome of an organism… (more)

Subjects/Keywords: High-throughput sequencing; Parallel algorithms

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APA (6th Edition):

Jammula, N. (2019). Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61740

Chicago Manual of Style (16th Edition):

Jammula, Nagakishore. “Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets.” 2019. Doctoral Dissertation, Georgia Tech. Accessed December 05, 2020. http://hdl.handle.net/1853/61740.

MLA Handbook (7th Edition):

Jammula, Nagakishore. “Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets.” 2019. Web. 05 Dec 2020.

Vancouver:

Jammula N. Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1853/61740.

Council of Science Editors:

Jammula N. Parallel algorithms for enabling fast and scalable analysis of high-throughput sequencing datasets. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61740

7. Bryant, Douglas W. (Douglas Wesley). Algorithms for massive biological datasets.

Degree: PhD, Computer Science, 2011, Oregon State University

 Within the past several years the technology of high-throughput sequencing has transformed the study of biology by offering unprecedented access to life's fundamental building block,… (more)

Subjects/Keywords: High-throughput sequencing; Nucleotide sequence  – Computer programs

…relating to high-throughput sequencing (HTS). Assembly, (1), is a… …x5D; 2 1.1 Introduction High-throughput sequencing technology has transformed the… …the-art methods for stitching short reads, the output of high-throughput sequencing… …several topics relating to high-throughput sequencing (HTS). Assembly, (1)… …Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 128 7.3 High-Throughput… 

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APA (6th Edition):

Bryant, D. W. (. W. (2011). Algorithms for massive biological datasets. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/25504

Chicago Manual of Style (16th Edition):

Bryant, Douglas W (Douglas Wesley). “Algorithms for massive biological datasets.” 2011. Doctoral Dissertation, Oregon State University. Accessed December 05, 2020. http://hdl.handle.net/1957/25504.

MLA Handbook (7th Edition):

Bryant, Douglas W (Douglas Wesley). “Algorithms for massive biological datasets.” 2011. Web. 05 Dec 2020.

Vancouver:

Bryant DW(W. Algorithms for massive biological datasets. [Internet] [Doctoral dissertation]. Oregon State University; 2011. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1957/25504.

Council of Science Editors:

Bryant DW(W. Algorithms for massive biological datasets. [Doctoral Dissertation]. Oregon State University; 2011. Available from: http://hdl.handle.net/1957/25504


Universidade Estadual de Campinas

8. Silveira, Karina da Costa, 1989-. O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: The molecular investigation of the skeletal dysplasias, also known as osteochondrodysplasias (OCD), is critical for both the accuracy of diagnosis and genetic counseling. Although… (more)

Subjects/Keywords: Osteocondrodisplasias; Doenças do desenvolvimento ósseo; Sequenciamento de nucleotídeos em larga escala; Osteochondrodysplasias; Bone diseases, Developmental; High-throughput nucleotide sequencing

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APA (6th Edition):

Silveira, Karina da Costa, 1. (2018). O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/331711

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silveira, Karina da Costa, 1989-. “O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias.” 2018. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/331711.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silveira, Karina da Costa, 1989-. “O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias.” 2018. Web. 05 Dec 2020.

Vancouver:

Silveira, Karina da Costa 1. O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331711.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Silveira, Karina da Costa 1. O sequenciamento de alto desempenho no diagnóstico das displasias esqueléticas = The next-generation sequencing in the diagnosis of skeletal dysplasias: The next-generation sequencing in the diagnosis of skeletal dysplasias. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331711

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

9. Bossolan, Ana Paula Oliveira Giorgetti, 1980-. Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development.

Degree: 2013, Universidade Estadual de Campinas

 Abstract: Considering the hypothesis that the mechanisms involved in periodontal regeneration mimic the mechanisms associated with the development of the original formation of the periodontium,… (more)

Subjects/Keywords: Genes; Periodonto; Dentes - Raizes; Lasers; Sequenciamento de nucleotídeos em larga escala; Genes; Periodontium; Polymerase Chain Reaction; Lasers; High-Throughput Nucleotide Sequencing

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APA (6th Edition):

Bossolan, Ana Paula Oliveira Giorgetti, 1. (2013). Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/289028

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bossolan, Ana Paula Oliveira Giorgetti, 1980-. “Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development.” 2013. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/289028.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bossolan, Ana Paula Oliveira Giorgetti, 1980-. “Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development.” 2013. Web. 05 Dec 2020.

Vancouver:

Bossolan, Ana Paula Oliveira Giorgetti 1. Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development. [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/289028.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bossolan, Ana Paula Oliveira Giorgetti 1. Padrão de expressão gênica na área do ligamento periodontal durante o desenvolvimento radicuar: Patterns of gene expression in mouse periodontal ligament during tooth root development. [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/289028

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

10. Svidnicki, Paulo Vinicius, 1989-. Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: Glaucoma is a neurodegenerative disease of multifactorial etiology that includes several eye disorders whose common features are the progressive damage of the optic nerve… (more)

Subjects/Keywords: Glaucoma; Genes; Sequenciamento de nucleotídeos em larga escala; Mutação; Glaucoma; Genes; High-throughput nucleotide sequencing; Mutation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Svidnicki, Paulo Vinicius, 1. (2018). Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/333588

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Svidnicki, Paulo Vinicius, 1989-. “Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma.” 2018. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/333588.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Svidnicki, Paulo Vinicius, 1989-. “Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma.” 2018. Web. 05 Dec 2020.

Vancouver:

Svidnicki, Paulo Vinicius 1. Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/333588.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Svidnicki, Paulo Vinicius 1. Análise de aspectos genéticos do glaucoma primário de ângulo aberto juvenil: Study of genetics aspects of juvenile open angle glaucoma. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/333588

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

11. Venn, Oliver Claude. Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing.

Degree: PhD, 2013, University of Oxford

 In eukaryotes, recombination plays a critical role in both the production of viable gametes and as a population genetic process. Here, we are interested in… (more)

Subjects/Keywords: 611.0181663; Medical Sciences; Mathematical genetics and bioinformatics (statistics); Genetic recombination; meiosis; high-throughput nucleotide sequencing; molecular evolution; comparative genomics

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APA (6th Edition):

Venn, O. C. (2013). Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960

Chicago Manual of Style (16th Edition):

Venn, Oliver Claude. “Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing.” 2013. Doctoral Dissertation, University of Oxford. Accessed December 05, 2020. http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960.

MLA Handbook (7th Edition):

Venn, Oliver Claude. “Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing.” 2013. Web. 05 Dec 2020.

Vancouver:

Venn OC. Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Dec 05]. Available from: http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960.

Council of Science Editors:

Venn OC. Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960


University of Helsinki

12. Vesanen, Kari. Genetic Background of familial B-cell lymphoma.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Tutkimukset ovat osoittaneet, että imusolmukesyöpien eli lymfoomien kehittymiseen liittyy suvuittainen riski. Tämän tutkimuksen tavoitteena oli löytää non-Hodgkin-lymfoomille altistava geenivirhe suomalaisen sukupuun henkilöiltä. Tutkimuksen kohteena olevasta… (more)

Subjects/Keywords: Genetics; Neoplasms; Lymphoma; Lymphoma, B-Cell; Genetic Variation; High-Throughput Nucleotide Sequencing; Medical Genetics; Lääketieteellinen genetiikka ja perinnöllisyyslääketiede; Medicinsk genetik

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APA (6th Edition):

Vesanen, K. (2016). Genetic Background of familial B-cell lymphoma. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/160914

Chicago Manual of Style (16th Edition):

Vesanen, Kari. “Genetic Background of familial B-cell lymphoma.” 2016. Masters Thesis, University of Helsinki. Accessed December 05, 2020. http://hdl.handle.net/10138/160914.

MLA Handbook (7th Edition):

Vesanen, Kari. “Genetic Background of familial B-cell lymphoma.” 2016. Web. 05 Dec 2020.

Vancouver:

Vesanen K. Genetic Background of familial B-cell lymphoma. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10138/160914.

Council of Science Editors:

Vesanen K. Genetic Background of familial B-cell lymphoma. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/160914


Universidade Estadual de Campinas

13. Martins, Fábio Tadeu Arrojo, 1989-. Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss.

Degree: 2017, Universidade Estadual de Campinas

 Abstract: Hearing loss is the most common sensory deficit in humans, affecting approximately 5 % of the world population. In developed countries, one in every… (more)

Subjects/Keywords: Perda auditiva; Surdez; Genética; Sequenciamento de nucleotídeos em larga escala; Sequenciamento completo de exoma; Hearing loss; Deafness; Genetics; High-throughput nucleotide sequencing; Whole exome sequencing

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APA (6th Edition):

Martins, Fábio Tadeu Arrojo, 1. (2017). Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/325529

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Martins, Fábio Tadeu Arrojo, 1989-. “Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss.” 2017. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/325529.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Martins, Fábio Tadeu Arrojo, 1989-. “Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss.” 2017. Web. 05 Dec 2020.

Vancouver:

Martins, Fábio Tadeu Arrojo 1. Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss. [Internet] [Thesis]. Universidade Estadual de Campinas; 2017. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/325529.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Martins, Fábio Tadeu Arrojo 1. Sequenciamento paralelo massivo na identificação e caracterização de genes relacionados à perda auditiva: Massive parallel sequencing for identification and characterization of genes related to hearing loss. [Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/325529

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Helsinki

14. Karhu, Thomas. Exome sequencing reveals a novel disease-causing gene in a Finnish family.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 The main focus of this study is a Finnish family, in which four out of eight children presented with an unidentified disease causing a grave… (more)

Subjects/Keywords: UBA5; whole exome sequencing; disease-causing variants; High-Throughput Nucleotide Sequencing; exome; UBA5 protein; mutation; Medical Genetics; Lääketieteellinen genetiikka ja perinnöllisyyslääketiede; Medicinsk genetik

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APA (6th Edition):

Karhu, T. (2016). Exome sequencing reveals a novel disease-causing gene in a Finnish family. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/162944

Chicago Manual of Style (16th Edition):

Karhu, Thomas. “Exome sequencing reveals a novel disease-causing gene in a Finnish family.” 2016. Masters Thesis, University of Helsinki. Accessed December 05, 2020. http://hdl.handle.net/10138/162944.

MLA Handbook (7th Edition):

Karhu, Thomas. “Exome sequencing reveals a novel disease-causing gene in a Finnish family.” 2016. Web. 05 Dec 2020.

Vancouver:

Karhu T. Exome sequencing reveals a novel disease-causing gene in a Finnish family. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10138/162944.

Council of Science Editors:

Karhu T. Exome sequencing reveals a novel disease-causing gene in a Finnish family. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/162944


Cornell University

15. Wang, Zhen. High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification.

Degree: PhD, Genetics, 2014, Cornell University

 Short-read high-throughput sequencing is the most popular approach to collect massive amount of DNA sequence data at declining cost in nearly all fields of current… (more)

Subjects/Keywords: Population Genetics; Natural Selection; High-throughput Sequencing

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APA (6th Edition):

Wang, Z. (2014). High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38964

Chicago Manual of Style (16th Edition):

Wang, Zhen. “High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification.” 2014. Doctoral Dissertation, Cornell University. Accessed December 05, 2020. http://hdl.handle.net/1813/38964.

MLA Handbook (7th Edition):

Wang, Zhen. “High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification.” 2014. Web. 05 Dec 2020.

Vancouver:

Wang Z. High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1813/38964.

Council of Science Editors:

Wang Z. High-Throughput Sequencing And Natural Selection: Studies Of Recent Sweep Inferences And A New Computational Approach For Transcription Identification. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38964


University of Minnesota

16. Palani, Nagendra Prasad. Molecular multiplexing methods for genome-scale measurements.

Degree: PhD, Plant and Microbial Biology, 2018, University of Minnesota

 I present the utility of unique DNA barcodes to tag distinct genotypes and subsequently link them to phenotypes. Such molecular tagging allowed us to perform… (more)

Subjects/Keywords: functional genomics; high throughput; next generation sequencing

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APA (6th Edition):

Palani, N. P. (2018). Molecular multiplexing methods for genome-scale measurements. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/209124

Chicago Manual of Style (16th Edition):

Palani, Nagendra Prasad. “Molecular multiplexing methods for genome-scale measurements.” 2018. Doctoral Dissertation, University of Minnesota. Accessed December 05, 2020. http://hdl.handle.net/11299/209124.

MLA Handbook (7th Edition):

Palani, Nagendra Prasad. “Molecular multiplexing methods for genome-scale measurements.” 2018. Web. 05 Dec 2020.

Vancouver:

Palani NP. Molecular multiplexing methods for genome-scale measurements. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11299/209124.

Council of Science Editors:

Palani NP. Molecular multiplexing methods for genome-scale measurements. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/209124


Louisiana State University

17. Hird, Sarah Michelle. Novel computational tools and utilization of the gut microbiota for phylogeographic inference.

Degree: PhD, 2013, Louisiana State University

 Genetic data are frequently responsible for biological insight and recent advances in sequencing technology (high-throughput sequencing; HTS) have created massive DNA-sequence based datasets. While these… (more)

Subjects/Keywords: bioinformatics; high-throughput sequencing; gut microbiota

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APA (6th Edition):

Hird, S. M. (2013). Novel computational tools and utilization of the gut microbiota for phylogeographic inference. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-04112013-150610 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3458

Chicago Manual of Style (16th Edition):

Hird, Sarah Michelle. “Novel computational tools and utilization of the gut microbiota for phylogeographic inference.” 2013. Doctoral Dissertation, Louisiana State University. Accessed December 05, 2020. etd-04112013-150610 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3458.

MLA Handbook (7th Edition):

Hird, Sarah Michelle. “Novel computational tools and utilization of the gut microbiota for phylogeographic inference.” 2013. Web. 05 Dec 2020.

Vancouver:

Hird SM. Novel computational tools and utilization of the gut microbiota for phylogeographic inference. [Internet] [Doctoral dissertation]. Louisiana State University; 2013. [cited 2020 Dec 05]. Available from: etd-04112013-150610 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3458.

Council of Science Editors:

Hird SM. Novel computational tools and utilization of the gut microbiota for phylogeographic inference. [Doctoral Dissertation]. Louisiana State University; 2013. Available from: etd-04112013-150610 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3458


University of Georgia

18. Reid, St Patrick Marinho. Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos.

Degree: 2014, University of Georgia

 Sorghum is a major source of nutrition in developing countries. Additionally, among cereal grains sorghum has one of the smallest genomes, making it an excellent… (more)

Subjects/Keywords: ESTs; High-throughput sequencing; Bioinformatics; Sorghum; Germination

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APA (6th Edition):

Reid, S. P. M. (2014). Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/29293

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Reid, St Patrick Marinho. “Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos.” 2014. Thesis, University of Georgia. Accessed December 05, 2020. http://hdl.handle.net/10724/29293.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Reid, St Patrick Marinho. “Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos.” 2014. Web. 05 Dec 2020.

Vancouver:

Reid SPM. Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10724/29293.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Reid SPM. Analysis of expressed sequence tags (ESTs) from sorghum bicolor germinating embryos. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/29293

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Cappi, Carolina. Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo.

Degree: PhD, Psiquiatria, 2013, University of São Paulo

Estudos de variações genéticas raras têm caracterizado com sucesso regiões do genoma e processos biológicos envolvidos no risco de desenvolver transtornos psiquiátricos. Dentro deste contexto,… (more)

Subjects/Keywords: Análise mutacional de DNA; DNA mutacional analysis; Exoma; Exome; High-throughput nucleotide sequencing; Obsessive-compulsive disorder/genetics; Sequenciamento de nucleotídeos em larga escala; Transtorno obsessivo-compulsivo/genética

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APA (6th Edition):

Cappi, C. (2013). Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5142/tde-09092013-160344/ ;

Chicago Manual of Style (16th Edition):

Cappi, Carolina. “Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo.” 2013. Doctoral Dissertation, University of São Paulo. Accessed December 05, 2020. http://www.teses.usp.br/teses/disponiveis/5/5142/tde-09092013-160344/ ;.

MLA Handbook (7th Edition):

Cappi, Carolina. “Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo.” 2013. Web. 05 Dec 2020.

Vancouver:

Cappi C. Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2020 Dec 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5142/tde-09092013-160344/ ;.

Council of Science Editors:

Cappi C. Variações raras no genoma de pacientes com transtorno obsessivo-compulsivo. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/5/5142/tde-09092013-160344/ ;

20. Roy, Christian K. Putting the Pieces Together: Exons and piRNAs: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, RNA Therapeutics Institute, 2014, U of Massachusetts : Med

  Analysis of gene expression has undergone a technological revolution. What was impossible 6 years ago is now routine. High-throughput DNA sequencing machines capable of… (more)

Subjects/Keywords: DNA; Gene Expression; Gene Expression Profiling; High-Throughput Nucleotide Sequencing; Protein Isoforms; RNA; Small Interfering RNA; DNA Sequence Analysis; Transcriptome; Biochemistry; Bioinformatics; Computational Biology; Genetics; Genomics; Systems Biology

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APA (6th Edition):

Roy, C. K. (2014). Putting the Pieces Together: Exons and piRNAs: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/726

Chicago Manual of Style (16th Edition):

Roy, Christian K. “Putting the Pieces Together: Exons and piRNAs: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/726.

MLA Handbook (7th Edition):

Roy, Christian K. “Putting the Pieces Together: Exons and piRNAs: A Dissertation.” 2014. Web. 05 Dec 2020.

Vancouver:

Roy CK. Putting the Pieces Together: Exons and piRNAs: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/726.

Council of Science Editors:

Roy CK. Putting the Pieces Together: Exons and piRNAs: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/726

21. Heyer, Erin E. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, RNA Therapeutics Institute, 2015, U of Massachusetts : Med

  Deep sequencing of strand-specific cDNA libraries is now a ubiquitous tool for identifying and quantifying RNAs in diverse sample types. The accuracy of conclusions… (more)

Subjects/Keywords: High-Throughput Nucleotide Sequencing; Nucleotides; RNA; Gene Library; Open Reading Frames; Biochemistry; Bioinformatics; Cell Biology; Computational Biology; Genetics; Molecular Biology; Molecular Genetics

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APA (6th Edition):

Heyer, E. E. (2015). Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/810

Chicago Manual of Style (16th Edition):

Heyer, Erin E. “Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/810.

MLA Handbook (7th Edition):

Heyer, Erin E. “Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.” 2015. Web. 05 Dec 2020.

Vancouver:

Heyer EE. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/810.

Council of Science Editors:

Heyer EE. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/810

22. Jiang, Li. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  Sequence-function relationship is a fundamental question for many branches of modern biomedical research. It connects the primary sequence of proteins to the function of… (more)

Subjects/Keywords: Viral Proteins; Genomics; High-Throughput Nucleotide Sequencing; RNA Sequence Analysis; Mutation; Computational Biology; Ecology and Evolutionary Biology; Genomics; Molecular Biology; Structural Biology; Systems Biology

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APA (6th Edition):

Jiang, L. (2016). Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/854

Chicago Manual of Style (16th Edition):

Jiang, Li. “Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/854.

MLA Handbook (7th Edition):

Jiang, Li. “Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.” 2016. Web. 05 Dec 2020.

Vancouver:

Jiang L. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/854.

Council of Science Editors:

Jiang L. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/854

23. Wang, Wei. Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation.

Degree: Bioinformatics and Computational Biology, RNA Therapeutics Institute, 2015, U of Massachusetts : Med

  PIWI-interacting RNAs (piRNA) are a group of 23–35 nucleotide (nt) short RNAs that protect animal gonads from transposon activities. In Drosophila germ line, piRNAs… (more)

Subjects/Keywords: Small Interfering RNA; Argonaute Proteins; RNA Interference; Drosophila Proteins; High-Throughput Nucleotide Sequencing; DNA Transposable Elements; Biochemistry; Bioinformatics; Computational Biology; Molecular Biology; Molecular Genetics

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APA (6th Edition):

Wang, W. (2015). Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/805

Chicago Manual of Style (16th Edition):

Wang, Wei. “Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/805.

MLA Handbook (7th Edition):

Wang, Wei. “Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation.” 2015. Web. 05 Dec 2020.

Vancouver:

Wang W. Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/805.

Council of Science Editors:

Wang W. Unveiling Molecular Mechanisms of piRNA Pathway from Small Signals in Big Data: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/805

24. Brese, Robin L. Tissue Compartmentalization and Tropism of HIV-1: A Dissertation.

Degree: Immunology and Microbiology, Program in Molecular Medicine, 2016, U of Massachusetts : Med

  Despite the development of effective antiretroviral treatments, there is still no cure for HIV-1. Major barriers to HIV-1 eradication include the diversity of intrapatient… (more)

Subjects/Keywords: HIV-1; HIV Infections; Human Immunodeficiency Virus env Gene Products; High-Throughput Nucleotide Sequencing; Immunology and Infectious Disease; Tissues; Virology; Virus Diseases

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APA (6th Edition):

Brese, R. L. (2016). Tissue Compartmentalization and Tropism of HIV-1: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/859

Chicago Manual of Style (16th Edition):

Brese, Robin L. “Tissue Compartmentalization and Tropism of HIV-1: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 05, 2020. http://escholarship.umassmed.edu/gsbs_diss/859.

MLA Handbook (7th Edition):

Brese, Robin L. “Tissue Compartmentalization and Tropism of HIV-1: A Dissertation.” 2016. Web. 05 Dec 2020.

Vancouver:

Brese RL. Tissue Compartmentalization and Tropism of HIV-1: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2020 Dec 05]. Available from: http://escholarship.umassmed.edu/gsbs_diss/859.

Council of Science Editors:

Brese RL. Tissue Compartmentalization and Tropism of HIV-1: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/859

25. Schaibley, Valerie Marie. Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing.

Degree: PhD, Human Genetics, 2013, University of Michigan

 Recent advances in high-throughput genome sequencing technology have paved the way for the field to gain a better understanding of single-nucleotide mutations in the human… (more)

Subjects/Keywords: Human Single-Nucleotide Mutation; High-Throughput Sequencing; Genetics; Science

Nucleotide Mutations and Their Downstream Effects on Human Health using High-Throughput Sequencing… …Association Study High-Throughput Sequencing Martin-Probst Syndrome Most Recent Common Ancestor… …advances in high-throughput genome sequencing technology have paved the way for the field to gain… …targeted regions using high-throughput sequencing (Ng et al. 2009). In a subsequent… …SNV identification in high-throughput sequencing studies is often error-prone, but results… 

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APA (6th Edition):

Schaibley, V. M. (2013). Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/97888

Chicago Manual of Style (16th Edition):

Schaibley, Valerie Marie. “Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing.” 2013. Doctoral Dissertation, University of Michigan. Accessed December 05, 2020. http://hdl.handle.net/2027.42/97888.

MLA Handbook (7th Edition):

Schaibley, Valerie Marie. “Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing.” 2013. Web. 05 Dec 2020.

Vancouver:

Schaibley VM. Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2027.42/97888.

Council of Science Editors:

Schaibley VM. Understanding the Patterns and Consequences of Single-Nucleotide Mutations in the Human Genome Using High-Throughput Sequencing. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/97888


Universidade Estadual de Campinas

26. Lima, Duane Fernandes de Souza, 1988-. Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade.

Degree: 2017, Universidade Estadual de Campinas

 Abstract: Myrcia s.l. is a large exclusively Neotropical group (ca. 750 species) that includes the traditional genera Myrcia, Marlierea and Calyptranthes. Recent phylogenetic studies based… (more)

Subjects/Keywords: Botânica - Classificação; Filogenia; Sequenciamento de nucleotídeos em larga escala; Revisão taxonômica; Morfologia vegetal; Plants - Classification; Phylogeny; High-throughput nucleotide sequencing; Taxonomic revisions; Plant morphology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lima, Duane Fernandes de Souza, 1. (2017). Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/331231

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lima, Duane Fernandes de Souza, 1988-. “Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade.” 2017. Thesis, Universidade Estadual de Campinas. Accessed December 05, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/331231.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lima, Duane Fernandes de Souza, 1988-. “Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade.” 2017. Web. 05 Dec 2020.

Vancouver:

Lima, Duane Fernandes de Souza 1. Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade. [Internet] [Thesis]. Universidade Estadual de Campinas; 2017. [cited 2020 Dec 05]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331231.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lima, Duane Fernandes de Souza 1. Estudos filogenéticos e taxonômicos em Myrcia DC. sensu lato (Myrtaceae), com ênfase no clado Guianensis = Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade: Phylogenetic and taxonomic studies in Myrcia DC. sensu lato (Myrtaceae), with emphasis on the Guianensis clade. [Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331231

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

27. Pfeifer, Susanne. Statistical challenges in the detection of mutation and variation using high throughput sequencing.

Degree: PhD, 2012, University of Oxford

 The aim of this thesis is to obtain a better understanding of mutation rates within as well as between the genomes of humans and chimpanzees… (more)

Subjects/Keywords: 611.01816; Bioinformatics (life sciences); Genetics (life sciences); Mathematical genetics and bioinformatics (statistics); genome-wide sequence variation; mutation rate; nucleotide diversity; long-term balancing selection; high throughput sequencing

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pfeifer, S. (2012). Statistical challenges in the detection of mutation and variation using high throughput sequencing. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605

Chicago Manual of Style (16th Edition):

Pfeifer, Susanne. “Statistical challenges in the detection of mutation and variation using high throughput sequencing.” 2012. Doctoral Dissertation, University of Oxford. Accessed December 05, 2020. http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605.

MLA Handbook (7th Edition):

Pfeifer, Susanne. “Statistical challenges in the detection of mutation and variation using high throughput sequencing.” 2012. Web. 05 Dec 2020.

Vancouver:

Pfeifer S. Statistical challenges in the detection of mutation and variation using high throughput sequencing. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Dec 05]. Available from: http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605.

Council of Science Editors:

Pfeifer S. Statistical challenges in the detection of mutation and variation using high throughput sequencing. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605


Universidad de Extremadura

28. Calvo Cano, Antonia María. Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico .

Degree: 2018, Universidad de Extremadura

 INTRODUCCIÓN: En la endocarditis infecciosa (EI) el hemocultivo no siempre es diagnóstico. La negatividad puede ser debida a bacterias zoonóticas. El presente trabajo analiza el… (more)

Subjects/Keywords: Endocarditis bacteriana; Enfermedades de las válvulas cardíacas; Secuenciación de alto rendimiento de nucleótidos; Endocarditis / diagnosis; Heart valves / microbiology; High-throughput nucleotide sequencing

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Calvo Cano, A. M. (2018). Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico . (Thesis). Universidad de Extremadura. Retrieved from http://hdl.handle.net/10662/7789

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Calvo Cano, Antonia María. “Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico .” 2018. Thesis, Universidad de Extremadura. Accessed December 05, 2020. http://hdl.handle.net/10662/7789.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Calvo Cano, Antonia María. “Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico .” 2018. Web. 05 Dec 2020.

Vancouver:

Calvo Cano AM. Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico . [Internet] [Thesis]. Universidad de Extremadura; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10662/7789.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Calvo Cano AM. Endocarditis con hemocultivos negativos en Extremadura. Papel de las técnicas de alta resolución en el diagnóstico etiológico . [Thesis]. Universidad de Extremadura; 2018. Available from: http://hdl.handle.net/10662/7789

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – Santa Cruz

29. Kim, Hyunsung John. Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics.

Degree: Biomolecular Engineering and Bioinformatics, 2014, University of California – Santa Cruz

High throughput sequencing methods have fundamentally shifted the manner in which biological experiments are performed. In this dissertation, conventional and novel high throughput sequencing and… (more)

Subjects/Keywords: Bioinformatics; Immunology; Antibiotic Resistance; High Throughput Sequencing; HLA typing; Next Generation Sequencing; Sequencing; T-cell Receptor Sequencing

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kim, H. J. (2014). Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/10g3n4hk

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kim, Hyunsung John. “Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics.” 2014. Thesis, University of California – Santa Cruz. Accessed December 05, 2020. http://www.escholarship.org/uc/item/10g3n4hk.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kim, Hyunsung John. “Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics.” 2014. Web. 05 Dec 2020.

Vancouver:

Kim HJ. Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics. [Internet] [Thesis]. University of California – Santa Cruz; 2014. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/10g3n4hk.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kim HJ. Applications of High Throughput Sequencing for Immunology and Clinical Diagnostics. [Thesis]. University of California – Santa Cruz; 2014. Available from: http://www.escholarship.org/uc/item/10g3n4hk

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Lincoln University

30. Kong, Hoi Yee. Development of a SNP validation toolset for wheat.

Degree: 2015, Lincoln University

 Recent advances in high-throughput technologies and the corresponding growth of the bioinformatics databases, a lot of bioinformatics tools have been constantly developed and published in… (more)

Subjects/Keywords: bioinformatics; high throughput sequencing analysis; reproducibility; virtualisation; single nucleotide polymorphism; marker assisted selection; cleaved amplified polymorphic sequence (CAPS); high resolution melting; wheat; containerisation; 080204 Mathematical Software; 060705 Plant Physiology; 070103 Agricultural Production Systems Simulation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kong, H. Y. (2015). Development of a SNP validation toolset for wheat. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/6777

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kong, Hoi Yee. “Development of a SNP validation toolset for wheat.” 2015. Thesis, Lincoln University. Accessed December 05, 2020. http://hdl.handle.net/10182/6777.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kong, Hoi Yee. “Development of a SNP validation toolset for wheat.” 2015. Web. 05 Dec 2020.

Vancouver:

Kong HY. Development of a SNP validation toolset for wheat. [Internet] [Thesis]. Lincoln University; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10182/6777.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kong HY. Development of a SNP validation toolset for wheat. [Thesis]. Lincoln University; 2015. Available from: http://hdl.handle.net/10182/6777

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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