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You searched for subject:(Next generation sequencing). Showing records 1 – 30 of 767 total matches.

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University of Sydney

1. Nafisinia, Michael. Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics .

Degree: 2017, University of Sydney

 The focus of this thesis was the identification of the genetic bases of Mendelian and mitochondrial respiratory chain disorders in a cohort of paediatric patients,… (more)

Subjects/Keywords: Next generation sequencing

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

APA (6th Edition):

Nafisinia, M. (2017). Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16867

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):

Nafisinia, Michael. “Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics .” 2017. Thesis, University of Sydney. Accessed August 10, 2020. http://hdl.handle.net/2123/16867.

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

MLA Handbook (7th Edition):

Nafisinia, Michael. “Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics .” 2017. Web. 10 Aug 2020.

Vancouver:

Nafisinia M. Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics . [Internet] [Thesis]. University of Sydney; 2017. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/2123/16867.

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

Council of Science Editors:

Nafisinia M. Gene Discovery for Genetic Disorders using Next Generation Sequencing and Functional Genomics . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/16867

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


Université de Neuchâtel

2. Geiser, Céline. Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata".

Degree: 2014, Université de Neuchâtel

 Malgré des avancées phénoménales en biologie évolutive, les mécanismes qui mènent à la spéciation, le berceau de la biodiversité, ne sont toujours pas complètement déchiffrés.… (more)

Subjects/Keywords: next generation sequencing

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APA (6th Edition):

Geiser, C. (2014). Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata". (Thesis). Université de Neuchâtel. Retrieved from http://doc.rero.ch/record/257452

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):

Geiser, Céline. “Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata".” 2014. Thesis, Université de Neuchâtel. Accessed August 10, 2020. http://doc.rero.ch/record/257452.

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

MLA Handbook (7th Edition):

Geiser, Céline. “Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata".” 2014. Web. 10 Aug 2020.

Vancouver:

Geiser C. Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata". [Internet] [Thesis]. Université de Neuchâtel; 2014. [cited 2020 Aug 10]. Available from: http://doc.rero.ch/record/257452.

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

Council of Science Editors:

Geiser C. Genome evolution and mechanisms underlying reproductive isolation in the polyploid "Biscutella laevigata". [Thesis]. Université de Neuchâtel; 2014. Available from: http://doc.rero.ch/record/257452

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


University of Rochester

3. Glass, Carolyn. Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia.

Degree: PhD, 2014, University of Rochester

 Leukemia is the most common form of cancer among children and adolescents, and approximately 2,000 infants per year are diagnosed within their first year of… (more)

Subjects/Keywords: Leukemia; Next Generation Sequencing

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APA (6th Edition):

Glass, C. (2014). Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28976

Chicago Manual of Style (16th Edition):

Glass, Carolyn. “Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia.” 2014. Doctoral Dissertation, University of Rochester. Accessed August 10, 2020. http://hdl.handle.net/1802/28976.

MLA Handbook (7th Edition):

Glass, Carolyn. “Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia.” 2014. Web. 10 Aug 2020.

Vancouver:

Glass C. Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1802/28976.

Council of Science Editors:

Glass C. Identifying a Potential Molecular Therapeutic Target for MLL-AF9 Leukemia. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28976


Universiteit Utrecht

4. Hoek, G. van de. Identifying novel genes involved in congenital anomalies of the kidney and urinary tract.

Degree: 2013, Universiteit Utrecht

 The recent collation of a large patient cohort encompassing the complete CAKUT spectrum, the advent of next generation sequencing (NGS) and progress in bioinformatic developmental… (more)

Subjects/Keywords: Kidney disease; next generation sequencing

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APA (6th Edition):

Hoek, G. v. d. (2013). Identifying novel genes involved in congenital anomalies of the kidney and urinary tract. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/287149

Chicago Manual of Style (16th Edition):

Hoek, G van de. “Identifying novel genes involved in congenital anomalies of the kidney and urinary tract.” 2013. Masters Thesis, Universiteit Utrecht. Accessed August 10, 2020. http://dspace.library.uu.nl:8080/handle/1874/287149.

MLA Handbook (7th Edition):

Hoek, G van de. “Identifying novel genes involved in congenital anomalies of the kidney and urinary tract.” 2013. Web. 10 Aug 2020.

Vancouver:

Hoek Gvd. Identifying novel genes involved in congenital anomalies of the kidney and urinary tract. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Aug 10]. Available from: http://dspace.library.uu.nl:8080/handle/1874/287149.

Council of Science Editors:

Hoek Gvd. Identifying novel genes involved in congenital anomalies of the kidney and urinary tract. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/287149


Cornell University

5. Al Abri, Mohammed. Development Of Genomic Methods And Tools For An Equine Model .

Degree: 2015, Cornell University

 The advent of genomic analysis has identified regions of functional significance in several mammalian species. However, for horses, relatively little such work was done compared… (more)

Subjects/Keywords: Horse; Genomics; Next generation sequencing

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APA (6th Edition):

Al Abri, M. (2015). Development Of Genomic Methods And Tools For An Equine Model . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40974

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):

Al Abri, Mohammed. “Development Of Genomic Methods And Tools For An Equine Model .” 2015. Thesis, Cornell University. Accessed August 10, 2020. http://hdl.handle.net/1813/40974.

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

MLA Handbook (7th Edition):

Al Abri, Mohammed. “Development Of Genomic Methods And Tools For An Equine Model .” 2015. Web. 10 Aug 2020.

Vancouver:

Al Abri M. Development Of Genomic Methods And Tools For An Equine Model . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1813/40974.

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

Council of Science Editors:

Al Abri M. Development Of Genomic Methods And Tools For An Equine Model . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40974

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


University of New South Wales

6. Deveson, Ira. Three (largely unrelated) experiments in the age of next-generation sequencing.

Degree: Biotechnology & Biomolecular Sciences, 2017, University of New South Wales

Next generation sequencing (NGS) enables researchers to identify instances of genetic variation and measure gene expression in an unbiased, global fashion. In this thesis I… (more)

Subjects/Keywords: Next-generation sequencing; Genomics; Transcriptomics

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APA (6th Edition):

Deveson, I. (2017). Three (largely unrelated) experiments in the age of next-generation sequencing. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58940 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48001/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Deveson, Ira. “Three (largely unrelated) experiments in the age of next-generation sequencing.” 2017. Doctoral Dissertation, University of New South Wales. Accessed August 10, 2020. http://handle.unsw.edu.au/1959.4/58940 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48001/SOURCE02?view=true.

MLA Handbook (7th Edition):

Deveson, Ira. “Three (largely unrelated) experiments in the age of next-generation sequencing.” 2017. Web. 10 Aug 2020.

Vancouver:

Deveson I. Three (largely unrelated) experiments in the age of next-generation sequencing. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2020 Aug 10]. Available from: http://handle.unsw.edu.au/1959.4/58940 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48001/SOURCE02?view=true.

Council of Science Editors:

Deveson I. Three (largely unrelated) experiments in the age of next-generation sequencing. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58940 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48001/SOURCE02?view=true


University of Minnesota

7. Cradic, Kendall. Next Generation Sequencing: Applications for the Clinic.

Degree: PhD, Biomedical Informatics and Computational Biology, 2016, University of Minnesota

 Genomic information from the patient is becoming increasingly important for diagnosis of many diseases. Next Generation Sequencing (NGS), while commonly used as a research tool,… (more)

Subjects/Keywords: haplotyping; next generation sequencing

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APA (6th Edition):

Cradic, K. (2016). Next Generation Sequencing: Applications for the Clinic. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182252

Chicago Manual of Style (16th Edition):

Cradic, Kendall. “Next Generation Sequencing: Applications for the Clinic.” 2016. Doctoral Dissertation, University of Minnesota. Accessed August 10, 2020. http://hdl.handle.net/11299/182252.

MLA Handbook (7th Edition):

Cradic, Kendall. “Next Generation Sequencing: Applications for the Clinic.” 2016. Web. 10 Aug 2020.

Vancouver:

Cradic K. Next Generation Sequencing: Applications for the Clinic. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/11299/182252.

Council of Science Editors:

Cradic K. Next Generation Sequencing: Applications for the Clinic. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182252


University of Melbourne

8. Orlowski, Christian. Epigenetic responses to external stimuli in murine embryonic stem cells.

Degree: 2012, University of Melbourne

 The epigenetic mechanisms underlying the nuclear plasticity of embryonic stem cells have been a focus of intensive research in the past several years. The emergence… (more)

Subjects/Keywords: bioinformatics; next generation sequencing; epigenetics

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APA (6th Edition):

Orlowski, C. (2012). Epigenetic responses to external stimuli in murine embryonic stem cells. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37286

Chicago Manual of Style (16th Edition):

Orlowski, Christian. “Epigenetic responses to external stimuli in murine embryonic stem cells.” 2012. Doctoral Dissertation, University of Melbourne. Accessed August 10, 2020. http://hdl.handle.net/11343/37286.

MLA Handbook (7th Edition):

Orlowski, Christian. “Epigenetic responses to external stimuli in murine embryonic stem cells.” 2012. Web. 10 Aug 2020.

Vancouver:

Orlowski C. Epigenetic responses to external stimuli in murine embryonic stem cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/11343/37286.

Council of Science Editors:

Orlowski C. Epigenetic responses to external stimuli in murine embryonic stem cells. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37286

9. Wong, Wallace K. Utilization Analysis of Reagents Used in Next Generation DNA Sequencing .

Degree: 2013, California State University – San Marcos

 Building on the Nobel Prize winning work of Dr. Fredrick Sanger, DNA sequencing has evolved into a high-throughput, massive parallel experimental system called Next Generation(more)

Subjects/Keywords: Next Generation Sequencing; Biotechnology; sequencing properties

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APA (6th Edition):

Wong, W. K. (2013). Utilization Analysis of Reagents Used in Next Generation DNA Sequencing . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.8/438

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):

Wong, Wallace K. “Utilization Analysis of Reagents Used in Next Generation DNA Sequencing .” 2013. Thesis, California State University – San Marcos. Accessed August 10, 2020. http://hdl.handle.net/10211.8/438.

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

MLA Handbook (7th Edition):

Wong, Wallace K. “Utilization Analysis of Reagents Used in Next Generation DNA Sequencing .” 2013. Web. 10 Aug 2020.

Vancouver:

Wong WK. Utilization Analysis of Reagents Used in Next Generation DNA Sequencing . [Internet] [Thesis]. California State University – San Marcos; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10211.8/438.

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

Council of Science Editors:

Wong WK. Utilization Analysis of Reagents Used in Next Generation DNA Sequencing . [Thesis]. California State University – San Marcos; 2013. Available from: http://hdl.handle.net/10211.8/438

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


Penn State University

10. Zhang, Zhenhai. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.

Degree: PhD, Integrative Biosciences, 2011, Penn State University

 The fundamental building block of eukaryotic genomes is the nucleosome, which consists of 147 base pairs DNA sequence and four core histones with possible exchange… (more)

Subjects/Keywords: Next-generation sequencing; data mining; ChIP-Seq

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APA (6th Edition):

Zhang, Z. (2011). DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11443

Chicago Manual of Style (16th Edition):

Zhang, Zhenhai. “DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.” 2011. Doctoral Dissertation, Penn State University. Accessed August 10, 2020. https://etda.libraries.psu.edu/catalog/11443.

MLA Handbook (7th Edition):

Zhang, Zhenhai. “DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.” 2011. Web. 10 Aug 2020.

Vancouver:

Zhang Z. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2020 Aug 10]. Available from: https://etda.libraries.psu.edu/catalog/11443.

Council of Science Editors:

Zhang Z. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/11443


Penn State University

11. Ratan, Aakrosh. ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA.

Degree: PhD, Computer Science and Engineering, 2009, Penn State University

Next-generation sequencing is revolutionizing genomics, promising higher coverage at a lower cost per base when compared to Sanger sequencing. Shorter reads and higher error rates… (more)

Subjects/Keywords: next-generation sequencing; genome assembly; algorithms

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APA (6th Edition):

Ratan, A. (2009). ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10300

Chicago Manual of Style (16th Edition):

Ratan, Aakrosh. “ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA.” 2009. Doctoral Dissertation, Penn State University. Accessed August 10, 2020. https://etda.libraries.psu.edu/catalog/10300.

MLA Handbook (7th Edition):

Ratan, Aakrosh. “ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA.” 2009. Web. 10 Aug 2020.

Vancouver:

Ratan A. ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Aug 10]. Available from: https://etda.libraries.psu.edu/catalog/10300.

Council of Science Editors:

Ratan A. ASSEMBLY ALGORITHMS FOR NEXT GENERATION SEQUENCE DATA. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10300


University of California – Riverside

12. Cacho, Ashley. Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model.

Degree: Applied Statistics, 2016, University of California – Riverside

 The emergence of high-throughput sequencing (HTS) technology has greatly influenced research in biological sciences including clinical applications such as in the understanding of disease etiology… (more)

Subjects/Keywords: Statistics; Bioinformatics; base-calling; next-generation sequencing

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APA (6th Edition):

Cacho, A. (2016). Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/98x9v8rn

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):

Cacho, Ashley. “Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model.” 2016. Thesis, University of California – Riverside. Accessed August 10, 2020. http://www.escholarship.org/uc/item/98x9v8rn.

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

MLA Handbook (7th Edition):

Cacho, Ashley. “Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model.” 2016. Web. 10 Aug 2020.

Vancouver:

Cacho A. Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model. [Internet] [Thesis]. University of California – Riverside; 2016. [cited 2020 Aug 10]. Available from: http://www.escholarship.org/uc/item/98x9v8rn.

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

Council of Science Editors:

Cacho A. Base-Calling of High-Throughput Sequencing Data Using a Random Effects Mixture Model. [Thesis]. University of California – Riverside; 2016. Available from: http://www.escholarship.org/uc/item/98x9v8rn

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


University of Otago

13. Sutton, Jolene Theresa. Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines .

Degree: 2013, University of Otago

 Theory predicts that rapid decreases in population size (“population bottlenecks”) will result in initial decreases in allelic diversity through a random sampling of individuals from… (more)

Subjects/Keywords: Philesturnus; Petroica; next generation sequencing; immunogenetics

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APA (6th Edition):

Sutton, J. T. (2013). Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4335

Chicago Manual of Style (16th Edition):

Sutton, Jolene Theresa. “Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines .” 2013. Doctoral Dissertation, University of Otago. Accessed August 10, 2020. http://hdl.handle.net/10523/4335.

MLA Handbook (7th Edition):

Sutton, Jolene Theresa. “Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines .” 2013. Web. 10 Aug 2020.

Vancouver:

Sutton JT. Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10523/4335.

Council of Science Editors:

Sutton JT. Major histocompatibility complex and microsatellite genetic diversity in bottlenecked populations of New Zealand passerines . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4335


Vanderbilt University

14. Hutchinson, Katherine Emily. Identification of Novel Targets for Therapy in Solid Tumors.

Degree: PhD, Cancer Biology, 2015, Vanderbilt University

 Solid tumor treatment paradigms have drastically improved in recent decades through direct targeting of the protein products of somatic, constitutively active âdriverâ mutations and their… (more)

Subjects/Keywords: next-generation sequencing; targeted therapy; cancer; melanoma

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APA (6th Edition):

Hutchinson, K. E. (2015). Identification of Novel Targets for Therapy in Solid Tumors. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-12112014-120700/ ;

Chicago Manual of Style (16th Edition):

Hutchinson, Katherine Emily. “Identification of Novel Targets for Therapy in Solid Tumors.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed August 10, 2020. http://etd.library.vanderbilt.edu//available/etd-12112014-120700/ ;.

MLA Handbook (7th Edition):

Hutchinson, Katherine Emily. “Identification of Novel Targets for Therapy in Solid Tumors.” 2015. Web. 10 Aug 2020.

Vancouver:

Hutchinson KE. Identification of Novel Targets for Therapy in Solid Tumors. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Aug 10]. Available from: http://etd.library.vanderbilt.edu//available/etd-12112014-120700/ ;.

Council of Science Editors:

Hutchinson KE. Identification of Novel Targets for Therapy in Solid Tumors. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu//available/etd-12112014-120700/ ;


Boston College

15. Indap, Amit R. Discovering rare variants from populations to families.

Degree: PhD, Biology, 2013, Boston College

 Partitioning an individual's phenotype into genetic and environmental components has been a major goal of genetics since the early 20th century. Formally, the proportion of… (more)

Subjects/Keywords: bioinformatics; human genetics; next generation sequencing

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APA (6th Edition):

Indap, A. R. (2013). Discovering rare variants from populations to families. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101399

Chicago Manual of Style (16th Edition):

Indap, Amit R. “Discovering rare variants from populations to families.” 2013. Doctoral Dissertation, Boston College. Accessed August 10, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101399.

MLA Handbook (7th Edition):

Indap, Amit R. “Discovering rare variants from populations to families.” 2013. Web. 10 Aug 2020.

Vancouver:

Indap AR. Discovering rare variants from populations to families. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2020 Aug 10]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101399.

Council of Science Editors:

Indap AR. Discovering rare variants from populations to families. [Doctoral Dissertation]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101399

16. Al Turki, Saeed. Integrated approaches to elucidate the genetic architecture of congenital heart defects.

Degree: PhD, 2014, University of Cambridge

 Congenital heart defects (CHD) are structural anomalies affecting the heart, are found in 1% of the population and arise during early stages of embryo development.… (more)

Subjects/Keywords: Congenital heart defects; Next generation sequencing

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APA (6th Edition):

Al Turki, S. (2014). Integrated approaches to elucidate the genetic architecture of congenital heart defects. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/245178https://www.repository.cam.ac.uk/bitstream/1810/245178/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/3/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/245178/6/sa9_thesis_corrected_13Jan2014.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/7/sa9_thesis_corrected_13Jan2014.pdf.jpg

Chicago Manual of Style (16th Edition):

Al Turki, Saeed. “Integrated approaches to elucidate the genetic architecture of congenital heart defects.” 2014. Doctoral Dissertation, University of Cambridge. Accessed August 10, 2020. https://www.repository.cam.ac.uk/handle/1810/245178https://www.repository.cam.ac.uk/bitstream/1810/245178/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/3/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/245178/6/sa9_thesis_corrected_13Jan2014.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/7/sa9_thesis_corrected_13Jan2014.pdf.jpg.

MLA Handbook (7th Edition):

Al Turki, Saeed. “Integrated approaches to elucidate the genetic architecture of congenital heart defects.” 2014. Web. 10 Aug 2020.

Vancouver:

Al Turki S. Integrated approaches to elucidate the genetic architecture of congenital heart defects. [Internet] [Doctoral dissertation]. University of Cambridge; 2014. [cited 2020 Aug 10]. Available from: https://www.repository.cam.ac.uk/handle/1810/245178https://www.repository.cam.ac.uk/bitstream/1810/245178/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/3/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/245178/6/sa9_thesis_corrected_13Jan2014.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/7/sa9_thesis_corrected_13Jan2014.pdf.jpg.

Council of Science Editors:

Al Turki S. Integrated approaches to elucidate the genetic architecture of congenital heart defects. [Doctoral Dissertation]. University of Cambridge; 2014. Available from: https://www.repository.cam.ac.uk/handle/1810/245178https://www.repository.cam.ac.uk/bitstream/1810/245178/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/3/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/245178/6/sa9_thesis_corrected_13Jan2014.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/245178/7/sa9_thesis_corrected_13Jan2014.pdf.jpg


University of Manitoba

17. Xu, Minqi. Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer.

Degree: Pathology, 2017, University of Manitoba

 Introduction: Modern care of patients with lung cancer requires rapid and accurate diagnosis leading to personalized therapies for individual patients based on molecular characteristics of… (more)

Subjects/Keywords: next generation sequencing; lung cancer; ALK; EGFR

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APA (6th Edition):

Xu, M. (2017). Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32390

Chicago Manual of Style (16th Edition):

Xu, Minqi. “Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer.” 2017. Masters Thesis, University of Manitoba. Accessed August 10, 2020. http://hdl.handle.net/1993/32390.

MLA Handbook (7th Edition):

Xu, Minqi. “Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer.” 2017. Web. 10 Aug 2020.

Vancouver:

Xu M. Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer. [Internet] [Masters thesis]. University of Manitoba; 2017. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1993/32390.

Council of Science Editors:

Xu M. Using next generation sequencing to detect clinically relevant oncogene mutations in lung cancer. [Masters Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32390


University of New South Wales

18. Roth Schulze, Alexandra Jazmin. Functional diversity and host-specificity of macroalgal surface-associated marine bacteria.

Degree: Biotechnology & Biomolecular Sciences, 2015, University of New South Wales

 Multicellular eukaryotic organisms live in constant interaction with microorganisms thatcolonise their surfaces. In the marine environment, macroalgae are colonised bycomplex communities of bacteria, however the… (more)

Subjects/Keywords: Next-generation sequencing; Microbial communities; Macroalgae

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APA (6th Edition):

Roth Schulze, A. J. (2015). Functional diversity and host-specificity of macroalgal surface-associated marine bacteria. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37505/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Roth Schulze, Alexandra Jazmin. “Functional diversity and host-specificity of macroalgal surface-associated marine bacteria.” 2015. Doctoral Dissertation, University of New South Wales. Accessed August 10, 2020. http://handle.unsw.edu.au/1959.4/55414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37505/SOURCE02?view=true.

MLA Handbook (7th Edition):

Roth Schulze, Alexandra Jazmin. “Functional diversity and host-specificity of macroalgal surface-associated marine bacteria.” 2015. Web. 10 Aug 2020.

Vancouver:

Roth Schulze AJ. Functional diversity and host-specificity of macroalgal surface-associated marine bacteria. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2020 Aug 10]. Available from: http://handle.unsw.edu.au/1959.4/55414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37505/SOURCE02?view=true.

Council of Science Editors:

Roth Schulze AJ. Functional diversity and host-specificity of macroalgal surface-associated marine bacteria. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37505/SOURCE02?view=true


University of Edinburgh

19. Emelianova, Katie. Using next generation sequencing to investigate the generation of diversity in the genus Begonia.

Degree: PhD, 2017, University of Edinburgh

 Begonia is one of the most diverse genera on the planet, with a species count approaching 2000 and a distribution across tropics in South America,… (more)

Subjects/Keywords: Begonia; plant evolution; next generation sequencing

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APA (6th Edition):

Emelianova, K. (2017). Using next generation sequencing to investigate the generation of diversity in the genus Begonia. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/29584

Chicago Manual of Style (16th Edition):

Emelianova, Katie. “Using next generation sequencing to investigate the generation of diversity in the genus Begonia.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed August 10, 2020. http://hdl.handle.net/1842/29584.

MLA Handbook (7th Edition):

Emelianova, Katie. “Using next generation sequencing to investigate the generation of diversity in the genus Begonia.” 2017. Web. 10 Aug 2020.

Vancouver:

Emelianova K. Using next generation sequencing to investigate the generation of diversity in the genus Begonia. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1842/29584.

Council of Science Editors:

Emelianova K. Using next generation sequencing to investigate the generation of diversity in the genus Begonia. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/29584


University College Cork

20. O'Sullivan, Daniel. The application of next generation sequencing to profile microbe related cheese quality defects.

Degree: 2015, University College Cork

 High throughput next generation sequencing, together with advanced molecular methods, has considerably enhanced the field of food microbiology. By overcoming biases associated with culture dependant… (more)

Subjects/Keywords: Microbiology; Next generation sequencing; Cheese defects

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APA (6th Edition):

O'Sullivan, D. (2015). The application of next generation sequencing to profile microbe related cheese quality defects. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/2809

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):

O'Sullivan, Daniel. “The application of next generation sequencing to profile microbe related cheese quality defects.” 2015. Thesis, University College Cork. Accessed August 10, 2020. http://hdl.handle.net/10468/2809.

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

MLA Handbook (7th Edition):

O'Sullivan, Daniel. “The application of next generation sequencing to profile microbe related cheese quality defects.” 2015. Web. 10 Aug 2020.

Vancouver:

O'Sullivan D. The application of next generation sequencing to profile microbe related cheese quality defects. [Internet] [Thesis]. University College Cork; 2015. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10468/2809.

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

Council of Science Editors:

O'Sullivan D. The application of next generation sequencing to profile microbe related cheese quality defects. [Thesis]. University College Cork; 2015. Available from: http://hdl.handle.net/10468/2809

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

21. Whitaker, Briana Kathleen. Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome .

Degree: 2018, Indiana University

 My dissertation research spans several topics in plant microbial ecology. In two research projects, I have explored whether host specificity influences fungal endophyte community structure… (more)

Subjects/Keywords: fungal endophytes; next generation sequencing; crops

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APA (6th Edition):

Whitaker, B. K. (2018). Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome . (Thesis). Indiana University. Retrieved from http://hdl.handle.net/2022/22316

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):

Whitaker, Briana Kathleen. “Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome .” 2018. Thesis, Indiana University. Accessed August 10, 2020. http://hdl.handle.net/2022/22316.

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

MLA Handbook (7th Edition):

Whitaker, Briana Kathleen. “Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome .” 2018. Web. 10 Aug 2020.

Vancouver:

Whitaker BK. Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome . [Internet] [Thesis]. Indiana University; 2018. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/2022/22316.

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

Council of Science Editors:

Whitaker BK. Host Specificity, Negative Feedbacks, and Pathogen Defense in the Plant Phyllosphere Microbiome . [Thesis]. Indiana University; 2018. Available from: http://hdl.handle.net/2022/22316

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


University of Toronto

22. Tam, Shirley. miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer.

Degree: PhD, 2015, University of Toronto

 Lung cancer is the leading cause of cancer death worldwide, with an estimated 1.8 million new cases diagnosed each year. Non-small cell lung cancer (NSCLC)… (more)

Subjects/Keywords: Lung Cancer; miRNA; Next-generation sequencing; 0307

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APA (6th Edition):

Tam, S. (2015). miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/71354

Chicago Manual of Style (16th Edition):

Tam, Shirley. “miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer.” 2015. Doctoral Dissertation, University of Toronto. Accessed August 10, 2020. http://hdl.handle.net/1807/71354.

MLA Handbook (7th Edition):

Tam, Shirley. “miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer.” 2015. Web. 10 Aug 2020.

Vancouver:

Tam S. miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1807/71354.

Council of Science Editors:

Tam S. miRNA Analysis by Next-generation Sequencing and its Prognostic Importance in Non-small Cell Lung Cancer. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/71354


University of Minnesota

23. 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 August 10, 2020. http://hdl.handle.net/11299/209124.

MLA Handbook (7th Edition):

Palani, Nagendra Prasad. “Molecular multiplexing methods for genome-scale measurements.” 2018. Web. 10 Aug 2020.

Vancouver:

Palani NP. Molecular multiplexing methods for genome-scale measurements. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2020 Aug 10]. 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


University of Melbourne

24. Garsed, Dale William. Genomic alterations in well- and de-differentiated liposarcoma.

Degree: 2013, University of Melbourne

 Well- and de-differentiated liposarcomas (WD/DDLPS) are tumours that arise from fat cells (adipocytes) and are characterised by the presence of supernumerary ring or ‘giant-rod’ marker… (more)

Subjects/Keywords: liposarcoma; genomics; neochromosome; NUP107; next-generation sequencing

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APA (6th Edition):

Garsed, D. W. (2013). Genomic alterations in well- and de-differentiated liposarcoma. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38387

Chicago Manual of Style (16th Edition):

Garsed, Dale William. “Genomic alterations in well- and de-differentiated liposarcoma.” 2013. Doctoral Dissertation, University of Melbourne. Accessed August 10, 2020. http://hdl.handle.net/11343/38387.

MLA Handbook (7th Edition):

Garsed, Dale William. “Genomic alterations in well- and de-differentiated liposarcoma.” 2013. Web. 10 Aug 2020.

Vancouver:

Garsed DW. Genomic alterations in well- and de-differentiated liposarcoma. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/11343/38387.

Council of Science Editors:

Garsed DW. Genomic alterations in well- and de-differentiated liposarcoma. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38387

25. Wang, Yi. Genome Assembly and Annotation of Isochrysis Galbana .

Degree: 2014, California State University – San Marcos

 Isochrysis Galbana is a species of cocoolithophores, which is a main factor of forming ocean's interior and sediments, and influencing the global cycles of carbon… (more)

Subjects/Keywords: Next-Generation Sequencing; Genome Assembly; Genome Annotation

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APA (6th Edition):

Wang, Y. (2014). Genome Assembly and Annotation of Isochrysis Galbana . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/120851

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, Yi. “Genome Assembly and Annotation of Isochrysis Galbana .” 2014. Thesis, California State University – San Marcos. Accessed August 10, 2020. http://hdl.handle.net/10211.3/120851.

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

MLA Handbook (7th Edition):

Wang, Yi. “Genome Assembly and Annotation of Isochrysis Galbana .” 2014. Web. 10 Aug 2020.

Vancouver:

Wang Y. Genome Assembly and Annotation of Isochrysis Galbana . [Internet] [Thesis]. California State University – San Marcos; 2014. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10211.3/120851.

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

Council of Science Editors:

Wang Y. Genome Assembly and Annotation of Isochrysis Galbana . [Thesis]. California State University – San Marcos; 2014. Available from: http://hdl.handle.net/10211.3/120851

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


Universitat de Valencia

26. García-García, Gema. Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform .

Degree: 2013, Universitat de Valencia

 El síndrome de Usher (USH) es una enfermedad hereditaria autosómica recesiva, caracterizada por la asociación de hipoacusia neurosensorial, retinosis pigmentaria y, en ocasiones, alteración de… (more)

Subjects/Keywords: next generation sequencing; usher syndrome; genetics

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APA (6th Edition):

García-García, G. (2013). Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/29081

Chicago Manual of Style (16th Edition):

García-García, Gema. “Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform .” 2013. Doctoral Dissertation, Universitat de Valencia. Accessed August 10, 2020. http://hdl.handle.net/10550/29081.

MLA Handbook (7th Edition):

García-García, Gema. “Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform .” 2013. Web. 10 Aug 2020.

Vancouver:

García-García G. Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10550/29081.

Council of Science Editors:

García-García G. Usher syndrome : molecular analysis of USH2 genes and development of a next-generation sequencing platform . [Doctoral Dissertation]. Universitat de Valencia; 2013. Available from: http://hdl.handle.net/10550/29081

27. Al Turki, Saeed. Integrated approaches to elucidate the genetic architecture of congenital heart defects.

Degree: PhD, 2014, University of Cambridge

 Congenital heart defects (CHD) are structural anomalies affecting the heart, are found in 1% of the population and arise during early stages of embryo development.… (more)

Subjects/Keywords: 616.1; Congenital heart defects; Next generation sequencing

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APA (6th Edition):

Al Turki, S. (2014). Integrated approaches to elucidate the genetic architecture of congenital heart defects. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/245178 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590265

Chicago Manual of Style (16th Edition):

Al Turki, Saeed. “Integrated approaches to elucidate the genetic architecture of congenital heart defects.” 2014. Doctoral Dissertation, University of Cambridge. Accessed August 10, 2020. https://www.repository.cam.ac.uk/handle/1810/245178 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590265.

MLA Handbook (7th Edition):

Al Turki, Saeed. “Integrated approaches to elucidate the genetic architecture of congenital heart defects.” 2014. Web. 10 Aug 2020.

Vancouver:

Al Turki S. Integrated approaches to elucidate the genetic architecture of congenital heart defects. [Internet] [Doctoral dissertation]. University of Cambridge; 2014. [cited 2020 Aug 10]. Available from: https://www.repository.cam.ac.uk/handle/1810/245178 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590265.

Council of Science Editors:

Al Turki S. Integrated approaches to elucidate the genetic architecture of congenital heart defects. [Doctoral Dissertation]. University of Cambridge; 2014. Available from: https://www.repository.cam.ac.uk/handle/1810/245178 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590265


Boston University

28. Dougherty, Kristen Elizabeth. Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer.

Degree: MS, Medical Sciences, 2015, Boston University

Next-Generation Sequencing has opened the doors to nearly limitless amounts of genomic data, but the clinical utility of this data is not yet clear. From… (more)

Subjects/Keywords: Genetics; Breast cancer; Hereditary cancer; Whole exome sequencing; Next generation sequencing

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APA (6th Edition):

Dougherty, K. E. (2015). Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16120

Chicago Manual of Style (16th Edition):

Dougherty, Kristen Elizabeth. “Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer.” 2015. Masters Thesis, Boston University. Accessed August 10, 2020. http://hdl.handle.net/2144/16120.

MLA Handbook (7th Edition):

Dougherty, Kristen Elizabeth. “Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer.” 2015. Web. 10 Aug 2020.

Vancouver:

Dougherty KE. Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/2144/16120.

Council of Science Editors:

Dougherty KE. Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16120


Montana Tech

29. Cosart, Ted. Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species.

Degree: PhD, 2013, Montana Tech

  The efficient method called exon capture provides for sequencing genes genome-wide, targeting candidate genes, and sampling specific exons within genes. Although developed for model… (more)

Subjects/Keywords: DNA Sequencing; Exon Capture; Next-generation Sequencing; Non-model species

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APA (6th Edition):

Cosart, T. (2013). Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/4133

Chicago Manual of Style (16th Edition):

Cosart, Ted. “Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species.” 2013. Doctoral Dissertation, Montana Tech. Accessed August 10, 2020. https://scholarworks.umt.edu/etd/4133.

MLA Handbook (7th Edition):

Cosart, Ted. “Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species.” 2013. Web. 10 Aug 2020.

Vancouver:

Cosart T. Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species. [Internet] [Doctoral dissertation]. Montana Tech; 2013. [cited 2020 Aug 10]. Available from: https://scholarworks.umt.edu/etd/4133.

Council of Science Editors:

Cosart T. Evaluation of a New Method for Large-Scale and Gene-targeted Next Generation DNA Sequencing in Nonmodel Species. [Doctoral Dissertation]. Montana Tech; 2013. Available from: https://scholarworks.umt.edu/etd/4133


Texas Medical Center

30. Zheng, Xiaofeng. DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS.

Degree: PhD, 2013, Texas Medical Center

Next-generation sequencing (NGS) technology has become a prominent tool in biological and biomedical research. However, NGS data analysis, such as de novo assembly, mapping… (more)

Subjects/Keywords: next-generation sequencing; sequencing error; error correction; SNP detection; Bioinformatics; Biostatistics

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APA (6th Edition):

Zheng, X. (2013). DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/338

Chicago Manual of Style (16th Edition):

Zheng, Xiaofeng. “DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed August 10, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/338.

MLA Handbook (7th Edition):

Zheng, Xiaofeng. “DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS.” 2013. Web. 10 Aug 2020.

Vancouver:

Zheng X. DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2020 Aug 10]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/338.

Council of Science Editors:

Zheng X. DEVELOPMENT OF NOVEL METHODS TO MINIMIZE THE IMPACT OF SEQUENCING ERRORS IN THE NEXT-GENERATION SEQUENCING DATA ANALYSIS. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/338

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