Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Genetic sequencing). Showing records 1 – 30 of 216 total matches.

[1] [2] [3] [4] [5] [6] [7] [8]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Helsinki

1. Mikkola, Annamari. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.

Degree: Medicinska fakulteten, 2018, University of Helsinki

 Tutkimuksen kohteena on suomalainen suku, jossa esiintyy hampaiden kovakudosten perinnöllinen kehityshäiriö. Aikaisemmissa tutkimuksissa kehityshäiriön aiheuttava mutaatio on paikallistettu kromosomiin 15, ja kahden näytteen eksomisekvensoinnilla on… (more)

Subjects/Keywords: Tooth abnormalities; genetic disorder; mutation; PCR; DNA Sequencing; Tooth abnormalities; genetic disorder; mutation; PCR; DNA Sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mikkola, A. (2018). Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/236398

Chicago Manual of Style (16th Edition):

Mikkola, Annamari. “Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.” 2018. Masters Thesis, University of Helsinki. Accessed January 18, 2020. http://hdl.handle.net/10138/236398.

MLA Handbook (7th Edition):

Mikkola, Annamari. “Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.” 2018. Web. 18 Jan 2020.

Vancouver:

Mikkola A. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10138/236398.

Council of Science Editors:

Mikkola A. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. [Masters Thesis]. University of Helsinki; 2018. Available from: http://hdl.handle.net/10138/236398


University of Cincinnati

2. Matias, Margret. Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results.

Degree: MS, Medicine: Genetic Counseling, 2017, University of Cincinnati

 Purpose: Whole exome sequencing (WES) has been found to be a useful clinical diagnostic tool; however, the effect of WES results on patient management has… (more)

Subjects/Keywords: Genetics; clinical impact; genetic counseling; genetic testing; medical management; whole exome sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Matias, M. (2017). Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1490352906282189

Chicago Manual of Style (16th Edition):

Matias, Margret. “Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results.” 2017. Masters Thesis, University of Cincinnati. Accessed January 18, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1490352906282189.

MLA Handbook (7th Edition):

Matias, Margret. “Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results.” 2017. Web. 18 Jan 2020.

Vancouver:

Matias M. Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results. [Internet] [Masters thesis]. University of Cincinnati; 2017. [cited 2020 Jan 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1490352906282189.

Council of Science Editors:

Matias M. Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results. [Masters Thesis]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1490352906282189

3. Takahashi, Mônica Miyuki. Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta).

Degree: Mestrado, Botânica, 2010, University of São Paulo

 Mitocôndrias são organelas semi-autônomas responsáveis pela respiração celular. Diversas fontes de evidências indicam a origem endossimbiótica dessas organelas, onde um organismo unicelular teria engolfado um… (more)

Subjects/Keywords: Genetic sequencing; Genomas; Genome; Gracilariaceae; Gracilariales; Rhodophyta; Rhodophyta; Sequenciamento genético

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Takahashi, M. M. (2010). Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta). (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41132/tde-06102010-164456/ ;

Chicago Manual of Style (16th Edition):

Takahashi, Mônica Miyuki. “Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta).” 2010. Masters Thesis, University of São Paulo. Accessed January 18, 2020. http://www.teses.usp.br/teses/disponiveis/41/41132/tde-06102010-164456/ ;.

MLA Handbook (7th Edition):

Takahashi, Mônica Miyuki. “Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta).” 2010. Web. 18 Jan 2020.

Vancouver:

Takahashi MM. Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta). [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Jan 18]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41132/tde-06102010-164456/ ;.

Council of Science Editors:

Takahashi MM. Sequenciamento e análise do genoma mitocondrial de Gracilaria tenuistipitata (Gracilariales, Rhodophyta). [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/41/41132/tde-06102010-164456/ ;

4. Dörr, Fabiane. Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação.

Degree: Mestrado, Biotecnologia, 2008, University of São Paulo

Amostras de água subterrânea provenientes de uma área industrial contaminada por hidrocarbonetos monoaromáticos foram utilizadas para a obtenção de bactérias degradadoras de BTEX (benzeno, tolueno,… (more)

Subjects/Keywords: Degradação ambiental; Environmental degradation; Genetic sequencing; Hidrocarbonetos; Hydrocarbons; Sequenciamento genético

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dörr, F. (2008). Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11042012-152743/ ;

Chicago Manual of Style (16th Edition):

Dörr, Fabiane. “Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação.” 2008. Masters Thesis, University of São Paulo. Accessed January 18, 2020. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11042012-152743/ ;.

MLA Handbook (7th Edition):

Dörr, Fabiane. “Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação.” 2008. Web. 18 Jan 2020.

Vancouver:

Dörr F. Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2020 Jan 18]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11042012-152743/ ;.

Council of Science Editors:

Dörr F. Consórcios degradadores de BTEX: isolamento, caracterização e avaliação do potencial de degradação. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11042012-152743/ ;


University of Cincinnati

5. Fisher, Rachel. Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey.

Degree: MS, Medicine: Genetic Counseling, 2015, University of Cincinnati

 Background: Whole exome sequencing (WES) is a genetic test that sequences all protein-coding regions, exons, in a patient’s genome. WES is used to identify disease… (more)

Subjects/Keywords: Genetics; Whole exome sequencing; Diagnostic odyssey; genetic testing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fisher, R. (2015). Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427813369

Chicago Manual of Style (16th Edition):

Fisher, Rachel. “Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey.” 2015. Masters Thesis, University of Cincinnati. Accessed January 18, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427813369.

MLA Handbook (7th Edition):

Fisher, Rachel. “Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey.” 2015. Web. 18 Jan 2020.

Vancouver:

Fisher R. Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey. [Internet] [Masters thesis]. University of Cincinnati; 2015. [cited 2020 Jan 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427813369.

Council of Science Editors:

Fisher R. Clinical whole exome sequencing in an academic pediatric hospital: A descriptive study of the diagnostic odyssey. [Masters Thesis]. University of Cincinnati; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427813369


Texas A&M University

6. Caldwell, Jana Denise. Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals.

Degree: 2014, Texas A&M University

 Musculoskeletal disorders are one of the leading causes of morality in neonatal Thoroughbred foals. Contracted Foal Syndrome (CFS) has accounted for up to 48% of… (more)

Subjects/Keywords: Thoroughbred; Foal; Genetic; Musculoskeletal; Congenital; Candidate genes; sequencing; GWAS; Classification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Caldwell, J. D. (2014). Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153856

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):

Caldwell, Jana Denise. “Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals.” 2014. Thesis, Texas A&M University. Accessed January 18, 2020. http://hdl.handle.net/1969.1/153856.

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

MLA Handbook (7th Edition):

Caldwell, Jana Denise. “Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals.” 2014. Web. 18 Jan 2020.

Vancouver:

Caldwell JD. Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1969.1/153856.

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

Council of Science Editors:

Caldwell JD. Investigation for Genetic Determinants of Flexion Contractures and Contracted Foal Syndrome in Neonatal Thoroughbred Foals. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153856

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


Universidade do Rio Grande do Sul

7. Vasconcelos, Ana Carina Nogueira. Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes.

Degree: 2018, Universidade do Rio Grande do Sul

O transplante de células germinativas tem sido uma importante abordagem experimental para o estudo da preservação genética de espécies ameaçadas de extinção ou economicamente importantes.… (more)

Subjects/Keywords: Peixe; Gene expression; Tambaqui; Marcador molecular; Genética; Germ cells; Genetic sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vasconcelos, A. C. N. (2018). Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/179274

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):

Vasconcelos, Ana Carina Nogueira. “Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes.” 2018. Thesis, Universidade do Rio Grande do Sul. Accessed January 18, 2020. http://hdl.handle.net/10183/179274.

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

MLA Handbook (7th Edition):

Vasconcelos, Ana Carina Nogueira. “Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes.” 2018. Web. 18 Jan 2020.

Vancouver:

Vasconcelos ACN. Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2018. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10183/179274.

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

Council of Science Editors:

Vasconcelos ACN. Implicações do uso de marcadores moleculares para o transplante de células germinativas em peixes. [Thesis]. Universidade do Rio Grande do Sul; 2018. Available from: http://hdl.handle.net/10183/179274

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


University of Southern California

8. Chen, Quan. Exploring the genetic basis of complex traits.

Degree: PhD, Computational Biology and Bioinformatics, 2014, University of Southern California

 This thesis aims to explore the genetic basis of complex traits. It addresses this problem in two parts. ❧ The first part stems from the… (more)

Subjects/Keywords: pooled sequencing; allele frequency; genetic overlap; disease relationship

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, Q. (2014). Exploring the genetic basis of complex traits. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/487384/rec/2668

Chicago Manual of Style (16th Edition):

Chen, Quan. “Exploring the genetic basis of complex traits.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/487384/rec/2668.

MLA Handbook (7th Edition):

Chen, Quan. “Exploring the genetic basis of complex traits.” 2014. Web. 18 Jan 2020.

Vancouver:

Chen Q. Exploring the genetic basis of complex traits. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/487384/rec/2668.

Council of Science Editors:

Chen Q. Exploring the genetic basis of complex traits. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/487384/rec/2668

9. Gillespie, Rachel Louise. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.

Degree: 2015, University of Manchester

 A comprehensive molecular and phenotypic analysis of congenital and childhood cataractRachel L. Gillespie; The University of Manchester, Doctor of Philosophy, 2015Congenital and childhood cataract (CCC)… (more)

Subjects/Keywords: cataract; syndrome; eye; next generation sequencing; diagnosis; personalised medicine; genetic heterogeneity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gillespie, R. L. (2015). A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:266030

Chicago Manual of Style (16th Edition):

Gillespie, Rachel Louise. “A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:266030.

MLA Handbook (7th Edition):

Gillespie, Rachel Louise. “A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.” 2015. Web. 18 Jan 2020.

Vancouver:

Gillespie RL. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:266030.

Council of Science Editors:

Gillespie RL. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:266030


University of Cambridge

10. Gilly, Arthur Leonard. Sequencing in Isolation: Next-generation sequencing studies in founder populations.

Degree: PhD, 2019, University of Cambridge

 Although common variants are routinely assayed in populations, rare mutations and copy-number variants are understudied contributors to the aetiology of complex traits. Isolated populations hold… (more)

Subjects/Keywords: whole-genome sequencing; genetic; association study; population isolate; structural variant

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gilly, A. L. (2019). Sequencing in Isolation: Next-generation sequencing studies in founder populations. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293403

Chicago Manual of Style (16th Edition):

Gilly, Arthur Leonard. “Sequencing in Isolation: Next-generation sequencing studies in founder populations.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 18, 2020. https://www.repository.cam.ac.uk/handle/1810/293403.

MLA Handbook (7th Edition):

Gilly, Arthur Leonard. “Sequencing in Isolation: Next-generation sequencing studies in founder populations.” 2019. Web. 18 Jan 2020.

Vancouver:

Gilly AL. Sequencing in Isolation: Next-generation sequencing studies in founder populations. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jan 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/293403.

Council of Science Editors:

Gilly AL. Sequencing in Isolation: Next-generation sequencing studies in founder populations. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293403


University of Melbourne

11. Perucca, Piero Cesare. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.

Degree: 2017, University of Melbourne

 Epilepsy is one of the most common neurological disorders, affecting people of all ages, races, social classes, and nationalities. It is characterised by an enduring… (more)

Subjects/Keywords: Epilepsy; Focal; Genetics; Genetic testing; Whole exome sequencing; Temporal lobe epilepsy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perucca, P. C. (2017). The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/194133

Chicago Manual of Style (16th Edition):

Perucca, Piero Cesare. “The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.” 2017. Doctoral Dissertation, University of Melbourne. Accessed January 18, 2020. http://hdl.handle.net/11343/194133.

MLA Handbook (7th Edition):

Perucca, Piero Cesare. “The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.” 2017. Web. 18 Jan 2020.

Vancouver:

Perucca PC. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/11343/194133.

Council of Science Editors:

Perucca PC. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/194133

12. Rife, Trevor W. Utilizing a historical wheat collection to develop new tools for modern plant breeding.

Degree: PhD, Genetics Interdepartmental Program, 2016, Kansas State University

 The Green Revolution is credited with saving billions of lives by effectively harnessing new genetic resources and breeding strategies to create high-yielding varieties for countries… (more)

Subjects/Keywords: plant breeding; genetic gain; genomic selection; genotyping-by-sequencing; phenoapps

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rife, T. W. (2016). Utilizing a historical wheat collection to develop new tools for modern plant breeding. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/34503

Chicago Manual of Style (16th Edition):

Rife, Trevor W. “Utilizing a historical wheat collection to develop new tools for modern plant breeding.” 2016. Doctoral Dissertation, Kansas State University. Accessed January 18, 2020. http://hdl.handle.net/2097/34503.

MLA Handbook (7th Edition):

Rife, Trevor W. “Utilizing a historical wheat collection to develop new tools for modern plant breeding.” 2016. Web. 18 Jan 2020.

Vancouver:

Rife TW. Utilizing a historical wheat collection to develop new tools for modern plant breeding. [Internet] [Doctoral dissertation]. Kansas State University; 2016. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2097/34503.

Council of Science Editors:

Rife TW. Utilizing a historical wheat collection to develop new tools for modern plant breeding. [Doctoral Dissertation]. Kansas State University; 2016. Available from: http://hdl.handle.net/2097/34503


Wayne State University

13. Stafford, Jaime Lyn. Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses.

Degree: PhD, Molecular Biology and Genetics, 2018, Wayne State University

  While 25% of ovarian cancer (OVCA) cases are due to inherited factors, most of the genetic risk remains unexplained. This study addressed this gap… (more)

Subjects/Keywords: cancer; genetic testing; ovarian; whole exome sequencing; Bioinformatics; Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stafford, J. L. (2018). Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1966

Chicago Manual of Style (16th Edition):

Stafford, Jaime Lyn. “Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses.” 2018. Doctoral Dissertation, Wayne State University. Accessed January 18, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1966.

MLA Handbook (7th Edition):

Stafford, Jaime Lyn. “Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses.” 2018. Web. 18 Jan 2020.

Vancouver:

Stafford JL. Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses. [Internet] [Doctoral dissertation]. Wayne State University; 2018. [cited 2020 Jan 18]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1966.

Council of Science Editors:

Stafford JL. Missing Heritability And Novel Germline Risk Loci In Hereditary Ovarian Cancer: Insights From Whole Exome Sequencing And Functional Analyses. [Doctoral Dissertation]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1966


University of Michigan

14. Flickinger, Matthew. Detecting and Correcting Contamination in Genetic Data.

Degree: PhD, Biostatistics, 2016, University of Michigan

 While technological innovation has dramatically increased the amount and variety of genomic data available to geneticists, no assay is perfect and both human error and… (more)

Subjects/Keywords: contamination; genetic sequencing; Genetics; Statistics and Numeric Data; Science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Flickinger, M. (2016). Detecting and Correcting Contamination in Genetic Data. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120783

Chicago Manual of Style (16th Edition):

Flickinger, Matthew. “Detecting and Correcting Contamination in Genetic Data.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 18, 2020. http://hdl.handle.net/2027.42/120783.

MLA Handbook (7th Edition):

Flickinger, Matthew. “Detecting and Correcting Contamination in Genetic Data.” 2016. Web. 18 Jan 2020.

Vancouver:

Flickinger M. Detecting and Correcting Contamination in Genetic Data. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2027.42/120783.

Council of Science Editors:

Flickinger M. Detecting and Correcting Contamination in Genetic Data. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120783


University of Guelph

15. Mohebalizadehgashti, Fatemeh. Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line .

Degree: 2016, University of Guelph

 The single model assembly line is a traditional type of assembly line, which assembles only one product in a large quantity. On the other hand,… (more)

Subjects/Keywords: Balancing; Sequencing; Mixed model assembly line; Hybrid genetic algorithm

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mohebalizadehgashti, F. (2016). Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9662

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):

Mohebalizadehgashti, Fatemeh. “Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line .” 2016. Thesis, University of Guelph. Accessed January 18, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9662.

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

MLA Handbook (7th Edition):

Mohebalizadehgashti, Fatemeh. “Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line .” 2016. Web. 18 Jan 2020.

Vancouver:

Mohebalizadehgashti F. Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line . [Internet] [Thesis]. University of Guelph; 2016. [cited 2020 Jan 18]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9662.

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

Council of Science Editors:

Mohebalizadehgashti F. Balancing, Sequencing and Determining the Number and Length of Workstations in a Mixed Model Assembly Line . [Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9662

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


Princeton University

16. Tikhonov, Mikhail. Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology .

Degree: PhD, 2014, Princeton University

 The wealth and complexity of the known microscopic detail of biological processes and pathways make the search for universality particularly challenging and appealing for a… (more)

Subjects/Keywords: embryonic development; genetic regulation; metagenomics; microbial ecology; precision; sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tikhonov, M. (2014). Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01k3569654f

Chicago Manual of Style (16th Edition):

Tikhonov, Mikhail. “Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology .” 2014. Doctoral Dissertation, Princeton University. Accessed January 18, 2020. http://arks.princeton.edu/ark:/88435/dsp01k3569654f.

MLA Handbook (7th Edition):

Tikhonov, Mikhail. “Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology .” 2014. Web. 18 Jan 2020.

Vancouver:

Tikhonov M. Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology . [Internet] [Doctoral dissertation]. Princeton University; 2014. [cited 2020 Jan 18]. Available from: http://arks.princeton.edu/ark:/88435/dsp01k3569654f.

Council of Science Editors:

Tikhonov M. Identifying details that matter: fruit fly development, genetic regulation, and microbial ecology . [Doctoral Dissertation]. Princeton University; 2014. Available from: http://arks.princeton.edu/ark:/88435/dsp01k3569654f


University of Sydney

17. Sandaradura, Sarah. Application of massively parallel sequencing approaches in Nemaline Myopathy .

Degree: 2018, University of Sydney

 Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional approach to diagnosis involved skeletal muscle biopsy followed by Sanger… (more)

Subjects/Keywords: congenital myopathy; genetic; neuromuscular; nemaline myopathy; massively parallel sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sandaradura, S. (2018). Application of massively parallel sequencing approaches in Nemaline Myopathy . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18998

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):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Thesis, University of Sydney. Accessed January 18, 2020. http://hdl.handle.net/2123/18998.

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

MLA Handbook (7th Edition):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Web. 18 Jan 2020.

Vancouver:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2123/18998.

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

Council of Science Editors:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18998

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


University of Cambridge

18. Gilly, Arthur Leonard. Sequencing in isolation : next-generation sequencing studies in founder populations.

Degree: PhD, 2019, University of Cambridge

 Although common variants are routinely assayed in populations, rare mutations and copy-number variants are understudied contributors to the aetiology of complex traits. Isolated populations hold… (more)

Subjects/Keywords: whole-genome sequencing; genetic; association study; population isolate; structural variant

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gilly, A. L. (2019). Sequencing in isolation : next-generation sequencing studies in founder populations. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293403 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782785

Chicago Manual of Style (16th Edition):

Gilly, Arthur Leonard. “Sequencing in isolation : next-generation sequencing studies in founder populations.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 18, 2020. https://www.repository.cam.ac.uk/handle/1810/293403 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782785.

MLA Handbook (7th Edition):

Gilly, Arthur Leonard. “Sequencing in isolation : next-generation sequencing studies in founder populations.” 2019. Web. 18 Jan 2020.

Vancouver:

Gilly AL. Sequencing in isolation : next-generation sequencing studies in founder populations. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jan 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/293403 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782785.

Council of Science Editors:

Gilly AL. Sequencing in isolation : next-generation sequencing studies in founder populations. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293403 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782785


University of Illinois – Urbana-Champaign

19. Han, Jennifer. Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits.

Degree: PhD, 0320, 2014, University of Illinois – Urbana-Champaign

 Sex chromosomes are found throughout many diverse lineages across the animal and plant kingdom. Most of the sex chromosomes that have been studied are well… (more)

Subjects/Keywords: Papaya; sex chromosome; dosage compensation; restriction-site associated DNA sequencing (RAD-seq); Ribonucleic acid sequencing (RNA-seq); gibberellin; genetic map

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Han, J. (2014). Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49690

Chicago Manual of Style (16th Edition):

Han, Jennifer. “Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 18, 2020. http://hdl.handle.net/2142/49690.

MLA Handbook (7th Edition):

Han, Jennifer. “Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits.” 2014. Web. 18 Jan 2020.

Vancouver:

Han J. Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2142/49690.

Council of Science Editors:

Han J. Sex chromosome evolution of papaya: Dynamic structural and expression changes and identification of associated traits. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49690

20. Perini, Ana Priscila. Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005.

Degree: PhD, Biotecnologia, 2012, University of São Paulo

Introdução: Os vírus parainfluenza são importante causa de infecções respiratórias. Na população pediátrica a doença característica associada com HPIV-1 e 2 é a laringotraqueobronquite, enquanto… (more)

Subjects/Keywords: Doenças infecciosas; Epidemiologia; Epidemiology; Genetic sequencing; Infectious diseases; Paramyxoviridae; Paramyxoviridae; Sequenciamento genético; Virologia; Virology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perini, A. P. (2012). Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-26112012-082543/ ;

Chicago Manual of Style (16th Edition):

Perini, Ana Priscila. “Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005.” 2012. Doctoral Dissertation, University of São Paulo. Accessed January 18, 2020. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-26112012-082543/ ;.

MLA Handbook (7th Edition):

Perini, Ana Priscila. “Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005.” 2012. Web. 18 Jan 2020.

Vancouver:

Perini AP. Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2020 Jan 18]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-26112012-082543/ ;.

Council of Science Editors:

Perini AP. Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-26112012-082543/ ;

21. Firnberg, Elad. Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code.

Degree: 2013, Johns Hopkins University

 Mutations are central to evolution, providing the genetic variation upon which selection acts. A mutation’s impact on fitness can be positive, negative, or neutral. Knowledge… (more)

Subjects/Keywords: fitness landscape; mutations; genetic code; distribution of fitness effects; mutagenesis; deep sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Firnberg, E. (2013). Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37043

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):

Firnberg, Elad. “Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code.” 2013. Thesis, Johns Hopkins University. Accessed January 18, 2020. http://jhir.library.jhu.edu/handle/1774.2/37043.

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

MLA Handbook (7th Edition):

Firnberg, Elad. “Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code.” 2013. Web. 18 Jan 2020.

Vancouver:

Firnberg E. Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code. [Internet] [Thesis]. Johns Hopkins University; 2013. [cited 2020 Jan 18]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37043.

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

Council of Science Editors:

Firnberg E. Protein Evolution: Mapping the Fitness Landscape and the Role of Constraints Imposed by the Genetic Code. [Thesis]. Johns Hopkins University; 2013. Available from: http://jhir.library.jhu.edu/handle/1774.2/37043

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


Université de Montréal

22. Hussin, Julie. Genomic variation in recombination patterns : implications for disease and cancer .

Degree: 2013, Université de Montréal

 Durant la méiose, il se produit des échanges réciproques entre fragments de chromosomes homologues par recombinaison génétique. Les chromosomes parentaux ainsi modifiés donnent naissance à… (more)

Subjects/Keywords: recombinaison génétique; séquençage; PRDM9; génétique des populations; leucémie; genetic recombination; sequencing; population genetics; leukemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hussin, J. (2013). Genomic variation in recombination patterns : implications for disease and cancer . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/10136

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):

Hussin, Julie. “Genomic variation in recombination patterns : implications for disease and cancer .” 2013. Thesis, Université de Montréal. Accessed January 18, 2020. http://hdl.handle.net/1866/10136.

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

MLA Handbook (7th Edition):

Hussin, Julie. “Genomic variation in recombination patterns : implications for disease and cancer .” 2013. Web. 18 Jan 2020.

Vancouver:

Hussin J. Genomic variation in recombination patterns : implications for disease and cancer . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1866/10136.

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

Council of Science Editors:

Hussin J. Genomic variation in recombination patterns : implications for disease and cancer . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/10136

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


University of Manchester

23. Gillespie, Rachel Louise. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.

Degree: PhD, 2015, University of Manchester

 A comprehensive molecular and phenotypic analysis of congenital and childhood cataractRachel L. Gillespie; The University of Manchester, Doctor of Philosophy, 2015Congenital and childhood cataract (CCC)… (more)

Subjects/Keywords: 618.92; cataract; syndrome; eye; next generation sequencing; diagnosis; personalised medicine; genetic heterogeneity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gillespie, R. L. (2015). A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-comprehensive-phenotypic-and-molecular-analysis-of-congenital-and-childhood-cataract(84c1f236-ba72-4fc3-862b-e28074a608f1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654834

Chicago Manual of Style (16th Edition):

Gillespie, Rachel Louise. “A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. https://www.research.manchester.ac.uk/portal/en/theses/a-comprehensive-phenotypic-and-molecular-analysis-of-congenital-and-childhood-cataract(84c1f236-ba72-4fc3-862b-e28074a608f1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654834.

MLA Handbook (7th Edition):

Gillespie, Rachel Louise. “A comprehensive phenotypic and molecular analysis of congenital and childhood cataract.” 2015. Web. 18 Jan 2020.

Vancouver:

Gillespie RL. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-comprehensive-phenotypic-and-molecular-analysis-of-congenital-and-childhood-cataract(84c1f236-ba72-4fc3-862b-e28074a608f1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654834.

Council of Science Editors:

Gillespie RL. A comprehensive phenotypic and molecular analysis of congenital and childhood cataract. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-comprehensive-phenotypic-and-molecular-analysis-of-congenital-and-childhood-cataract(84c1f236-ba72-4fc3-862b-e28074a608f1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654834


University of Southern California

24. Dunham, Joseph Paul. Cellular level bottlenecks: genetic diversity, population dynamics, and technology development.

Degree: PhD, Molecular Biology, 2015, University of Southern California

 This thesis was motivated by the recognition of the importance of the underlying role that genetic variation plays in disease and how this genetic variation… (more)

Subjects/Keywords: genomics; population bottlenecks; genetic diversity; planaria; ZYMV; next generation sequencing; mitochondria; cell‐to‐cell movement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dunham, J. P. (2015). Cellular level bottlenecks: genetic diversity, population dynamics, and technology development. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/531830/rec/1264

Chicago Manual of Style (16th Edition):

Dunham, Joseph Paul. “Cellular level bottlenecks: genetic diversity, population dynamics, and technology development.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/531830/rec/1264.

MLA Handbook (7th Edition):

Dunham, Joseph Paul. “Cellular level bottlenecks: genetic diversity, population dynamics, and technology development.” 2015. Web. 18 Jan 2020.

Vancouver:

Dunham JP. Cellular level bottlenecks: genetic diversity, population dynamics, and technology development. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/531830/rec/1264.

Council of Science Editors:

Dunham JP. Cellular level bottlenecks: genetic diversity, population dynamics, and technology development. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/531830/rec/1264


Harvard University

25. Christodoulou, Danos C. Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy.

Degree: PhD, Biology: Medical Sciences, Division of, 2013, Harvard University

 Characterization of the RNA transcriptome by next-generation sequencing can produce an unprecedented yield of information that provides novel biologic insights. I describe four approaches for… (more)

Subjects/Keywords: Genetics; fhl1; genetic modifier; hypertrophic cardiomyopathy; inherited cardiomyopathies; next-generation sequencing; rna-seq

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Christodoulou, D. C. (2013). Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156672

Chicago Manual of Style (16th Edition):

Christodoulou, Danos C. “Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy.” 2013. Doctoral Dissertation, Harvard University. Accessed January 18, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156672.

MLA Handbook (7th Edition):

Christodoulou, Danos C. “Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy.” 2013. Web. 18 Jan 2020.

Vancouver:

Christodoulou DC. Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Jan 18]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156672.

Council of Science Editors:

Christodoulou DC. Methods for comprehensive transcriptome analysis using next-generation sequencing and application in hypertrophic cardiomyopathy. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156672


Massey University

26. Yeoman, Carl. The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand .

Degree: 2009, Massey University

 Butyrivibrio proteoclasticus B316T is the most recently described species of the Butyrivibrio / Pseudobutyrivibrio assemblage and now the first to have its genome sequenced. The… (more)

Subjects/Keywords: Genetic sequencing; Replication; Butyrivibrio; Gene expression

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yeoman, C. (2009). The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand . (Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/983

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):

Yeoman, Carl. “The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand .” 2009. Thesis, Massey University. Accessed January 18, 2020. http://hdl.handle.net/10179/983.

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

MLA Handbook (7th Edition):

Yeoman, Carl. “The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand .” 2009. Web. 18 Jan 2020.

Vancouver:

Yeoman C. The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand . [Internet] [Thesis]. Massey University; 2009. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10179/983.

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

Council of Science Editors:

Yeoman C. The auxiliary replicons of Butyrivibrio proteoclasticus : a thesis presented in fulfilment of the Doctorate of Philosophy degree at Massey University, Palmerston North, New Zealand . [Thesis]. Massey University; 2009. Available from: http://hdl.handle.net/10179/983

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


Boise State University

27. Brinkmeyer, Michaela. Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management.

Degree: 2018, Boise State University

Genetic structure is useful for inferring patterns of selection, gene flow and connectivity, and can define management units that aid in interpretation of spatially-specific trends… (more)

Subjects/Keywords: population genomics; genetic structure; American Kestrel; next-generation sequencing; migration distance; migration; Biology; Population Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Brinkmeyer, M. (2018). Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management. (Thesis). Boise State University. Retrieved from https://scholarworks.boisestate.edu/td/1467

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):

Brinkmeyer, Michaela. “Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management.” 2018. Thesis, Boise State University. Accessed January 18, 2020. https://scholarworks.boisestate.edu/td/1467.

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

MLA Handbook (7th Edition):

Brinkmeyer, Michaela. “Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management.” 2018. Web. 18 Jan 2020.

Vancouver:

Brinkmeyer M. Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management. [Internet] [Thesis]. Boise State University; 2018. [cited 2020 Jan 18]. Available from: https://scholarworks.boisestate.edu/td/1467.

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

Council of Science Editors:

Brinkmeyer M. Patterns of Genetic Structure in the American Kestrel (Falco sparverius): Influence of Distance and Migration and Implications for Monitoring and Management. [Thesis]. Boise State University; 2018. Available from: https://scholarworks.boisestate.edu/td/1467

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


Univerzitet u Beogradu

28. Janković, Milena Z., 1982-. Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije.

Degree: Biološki fakultet, 2016, Univerzitet u Beogradu

Biologija - Medicinska genetika / Biology - Medical Genetics

Parkinsonova bolest je drugo najčešće neurodegenerativno oboljenje koje pogaĎa od 1% do 2% stanovništva starijeg od… (more)

Subjects/Keywords: Parkinson’s disease; PARK2; LRRK2; VPS35; GBA; mutation frequency; Serbia; genetic testing; direct sequencing; MLPA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Janković, Milena Z., 1. (2016). Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:10436/bdef:Content/get

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):

Janković, Milena Z., 1982-. “Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije.” 2016. Thesis, Univerzitet u Beogradu. Accessed January 18, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:10436/bdef:Content/get.

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

MLA Handbook (7th Edition):

Janković, Milena Z., 1982-. “Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije.” 2016. Web. 18 Jan 2020.

Vancouver:

Janković, Milena Z. 1. Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2020 Jan 18]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10436/bdef:Content/get.

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

Council of Science Editors:

Janković, Milena Z. 1. Studija genetičke osnove Parkinsonove bolesti kod stanovništva Srbije. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10436/bdef:Content/get

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


University of Melbourne

29. CANTACESSI, CINZIA. Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications.

Degree: 2011, University of Melbourne

 The objective of the present thesis was to characterise the transcriptomes (= messenger RNAs transcribed in an organism at any one time) of selected gastrointestinal… (more)

Subjects/Keywords: bioinformatics; parasite; next-generation sequencing; transcriptomics; drug targets; Ancylostoma-secreted proteins; nematode; genetic interactions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

CANTACESSI, C. (2011). Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36000

Chicago Manual of Style (16th Edition):

CANTACESSI, CINZIA. “Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications.” 2011. Doctoral Dissertation, University of Melbourne. Accessed January 18, 2020. http://hdl.handle.net/11343/36000.

MLA Handbook (7th Edition):

CANTACESSI, CINZIA. “Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications.” 2011. Web. 18 Jan 2020.

Vancouver:

CANTACESSI C. Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/11343/36000.

Council of Science Editors:

CANTACESSI C. Genomic-bioinformatic investigations of key gastrointestinal parasites of socio-economic importance and their implications. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36000


Brno University of Technology

30. Bartoň, Vojtěch. Analýza genetické variability v sekvenačních datech treponemálních kmenů .

Degree: 2018, Brno University of Technology

 Tato diplomová práce se zabývá metodami určení genetické variability v sekvenačních datech. Sekvenovaným organismem je několik kmenů bakterie Treponema pallidum. Bakterie byly osekvenovány na platformě… (more)

Subjects/Keywords: heterogenita; bioinformatika; Treponema pallidum; genetická variabilita; sekvenace; heterogeneity; bioinformatics; Treponema pallidum; genetic variability; sequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bartoň, V. (2018). Analýza genetické variability v sekvenačních datech treponemálních kmenů . (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/82050

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):

Bartoň, Vojtěch. “Analýza genetické variability v sekvenačních datech treponemálních kmenů .” 2018. Thesis, Brno University of Technology. Accessed January 18, 2020. http://hdl.handle.net/11012/82050.

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

MLA Handbook (7th Edition):

Bartoň, Vojtěch. “Analýza genetické variability v sekvenačních datech treponemálních kmenů .” 2018. Web. 18 Jan 2020.

Vancouver:

Bartoň V. Analýza genetické variability v sekvenačních datech treponemálních kmenů . [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/11012/82050.

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

Council of Science Editors:

Bartoň V. Analýza genetické variability v sekvenačních datech treponemálních kmenů . [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/82050

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

[1] [2] [3] [4] [5] [6] [7] [8]

.