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You searched for subject:(Mathematical genetics AND bioinformatics statistics ). Showing records 1 – 30 of 720 total matches.

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University of Oxford

1. Anderson, James William Justin. Probabilistic models of RNA secondary structure.

Degree: PhD, 2013, University of Oxford

 This thesis develops probabilistic models of RNA secondary structure. The first chapter introduces RNA secondary structure prediction, in particular stochastic context-free grammars (SCFGs), and considers… (more)

Subjects/Keywords: 572.88; Mathematical genetics and bioinformatics (statistics); bioinformatics; RNA secondary structure

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

APA (6th Edition):

Anderson, J. W. J. (2013). Probabilistic models of RNA secondary structure. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:3e58e9d9-c58d-4616-8e88-4082d1ca0e2a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581305

Chicago Manual of Style (16th Edition):

Anderson, James William Justin. “Probabilistic models of RNA secondary structure.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:3e58e9d9-c58d-4616-8e88-4082d1ca0e2a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581305.

MLA Handbook (7th Edition):

Anderson, James William Justin. “Probabilistic models of RNA secondary structure.” 2013. Web. 20 Jan 2020.

Vancouver:

Anderson JWJ. Probabilistic models of RNA secondary structure. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:3e58e9d9-c58d-4616-8e88-4082d1ca0e2a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581305.

Council of Science Editors:

Anderson JWJ. Probabilistic models of RNA secondary structure. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:3e58e9d9-c58d-4616-8e88-4082d1ca0e2a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581305


University of Oxford

2. Forest, Marie. Simultaneous estimation of population size changes and splits times using importance sampling.

Degree: PhD, 2014, University of Oxford

 The genome is a treasure trove of information about the history of an individual, his population, and his species. For as long as genomic data… (more)

Subjects/Keywords: 572.8; Mathematical genetics and bioinformatics (statistics); Stochastic processes; Statistics; methodology; population history; coalescent theory; genetics

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APA (6th Edition):

Forest, M. (2014). Simultaneous estimation of population size changes and splits times using importance sampling. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8c067a3d-44d5-468a-beb5-34c5830998c4 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644707

Chicago Manual of Style (16th Edition):

Forest, Marie. “Simultaneous estimation of population size changes and splits times using importance sampling.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:8c067a3d-44d5-468a-beb5-34c5830998c4 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644707.

MLA Handbook (7th Edition):

Forest, Marie. “Simultaneous estimation of population size changes and splits times using importance sampling.” 2014. Web. 20 Jan 2020.

Vancouver:

Forest M. Simultaneous estimation of population size changes and splits times using importance sampling. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:8c067a3d-44d5-468a-beb5-34c5830998c4 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644707.

Council of Science Editors:

Forest M. Simultaneous estimation of population size changes and splits times using importance sampling. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:8c067a3d-44d5-468a-beb5-34c5830998c4 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644707


Princeton University

3. Robinson, David Garrett. The role of read depth in the design and analysis of sequencing experiments.

Degree: 2015, Princeton University

  The development of quantitative sequencing technologies, such as RNA-Seq, Bar-Seq, ChIP-Seq, and metagenomics, has offered great insight into molecular biology. Proper design and analysis… (more)

Subjects/Keywords: Genetics; Statistics; Bioinformatics

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APA (6th Edition):

Robinson, D. G. (2015). The role of read depth in the design and analysis of sequencing experiments. (Thesis). Princeton University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3713946

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):

Robinson, David Garrett. “The role of read depth in the design and analysis of sequencing experiments.” 2015. Thesis, Princeton University. Accessed January 20, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3713946.

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

MLA Handbook (7th Edition):

Robinson, David Garrett. “The role of read depth in the design and analysis of sequencing experiments.” 2015. Web. 20 Jan 2020.

Vancouver:

Robinson DG. The role of read depth in the design and analysis of sequencing experiments. [Internet] [Thesis]. Princeton University; 2015. [cited 2020 Jan 20]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3713946.

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

Council of Science Editors:

Robinson DG. The role of read depth in the design and analysis of sequencing experiments. [Thesis]. Princeton University; 2015. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3713946

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


University of Adelaide

4. Pfeiffer, Andrew James. A simulation study to compare gene set analysis methods.

Degree: 2016, University of Adelaide

 Genome-wide association studies (GWA studies) identify alleles that are associated with a disease. These allele variations are called single nucleotide polymorphisms (SNPs). However, GWA studies… (more)

Subjects/Keywords: genetics; bioinformatics; statistics

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APA (6th Edition):

Pfeiffer, A. J. (2016). A simulation study to compare gene set analysis methods. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/100190

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):

Pfeiffer, Andrew James. “A simulation study to compare gene set analysis methods.” 2016. Thesis, University of Adelaide. Accessed January 20, 2020. http://hdl.handle.net/2440/100190.

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

MLA Handbook (7th Edition):

Pfeiffer, Andrew James. “A simulation study to compare gene set analysis methods.” 2016. Web. 20 Jan 2020.

Vancouver:

Pfeiffer AJ. A simulation study to compare gene set analysis methods. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2440/100190.

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

Council of Science Editors:

Pfeiffer AJ. A simulation study to compare gene set analysis methods. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/100190

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


University of Oxford

5. Randall, Joshua Charles. Large-scale genetic analysis of quantitative traits.

Degree: PhD, 2012, University of Oxford

 Recent advances in genotyping technology coupled with an improved understanding of the architecture of linkage disequilibrium across the human genome have resulted in genome-wide association… (more)

Subjects/Keywords: 611.01816; Mathematical genetics and bioinformatics (statistics); Genetics (life sciences); meta-analysis; anthropometric; mega-analysis; genetics

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APA (6th Edition):

Randall, J. C. (2012). Large-scale genetic analysis of quantitative traits. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:addfb69d-602c-43e3-ab18-6e6d3b269076 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588395

Chicago Manual of Style (16th Edition):

Randall, Joshua Charles. “Large-scale genetic analysis of quantitative traits.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:addfb69d-602c-43e3-ab18-6e6d3b269076 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588395.

MLA Handbook (7th Edition):

Randall, Joshua Charles. “Large-scale genetic analysis of quantitative traits.” 2012. Web. 20 Jan 2020.

Vancouver:

Randall JC. Large-scale genetic analysis of quantitative traits. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:addfb69d-602c-43e3-ab18-6e6d3b269076 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588395.

Council of Science Editors:

Randall JC. Large-scale genetic analysis of quantitative traits. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:addfb69d-602c-43e3-ab18-6e6d3b269076 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588395


University of Oxford

6. Menelaou, Androniki. LD-based SNP and genotype calling from next-generation sequencing reads.

Degree: PhD, 2012, University of Oxford

 Next-generation sequencing is revolutionising in genetics, where base-by base information for the whole genome is available for a large sample of individuals. This type of… (more)

Subjects/Keywords: 572.8; Mathematical genetics and bioinformatics (statistics); sequencing; phasing; SNP-calling

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APA (6th Edition):

Menelaou, A. (2012). LD-based SNP and genotype calling from next-generation sequencing reads. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2093d498-3e7f-4648-9fde-fcdb311849de ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669933

Chicago Manual of Style (16th Edition):

Menelaou, Androniki. “LD-based SNP and genotype calling from next-generation sequencing reads.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:2093d498-3e7f-4648-9fde-fcdb311849de ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669933.

MLA Handbook (7th Edition):

Menelaou, Androniki. “LD-based SNP and genotype calling from next-generation sequencing reads.” 2012. Web. 20 Jan 2020.

Vancouver:

Menelaou A. LD-based SNP and genotype calling from next-generation sequencing reads. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:2093d498-3e7f-4648-9fde-fcdb311849de ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669933.

Council of Science Editors:

Menelaou A. LD-based SNP and genotype calling from next-generation sequencing reads. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:2093d498-3e7f-4648-9fde-fcdb311849de ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669933


University of Oxford

7. Miller, Luke Rex. Evolution of highly fecund organisms.

Degree: PhD, 2015, University of Oxford

 We develop and study the high-density limit of various new models in mathematical pop- ulation genetics. These models extend the Λ-Fleming–Viot process when there are… (more)

Subjects/Keywords: 576.5; Probability; Stochastic processes; Mathematical genetics and bioinformatics (statistics)

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APA (6th Edition):

Miller, L. R. (2015). Evolution of highly fecund organisms. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:60a9fcc7-b939-4075-be31-ed69014ad898 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664774

Chicago Manual of Style (16th Edition):

Miller, Luke Rex. “Evolution of highly fecund organisms.” 2015. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:60a9fcc7-b939-4075-be31-ed69014ad898 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664774.

MLA Handbook (7th Edition):

Miller, Luke Rex. “Evolution of highly fecund organisms.” 2015. Web. 20 Jan 2020.

Vancouver:

Miller LR. Evolution of highly fecund organisms. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:60a9fcc7-b939-4075-be31-ed69014ad898 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664774.

Council of Science Editors:

Miller LR. Evolution of highly fecund organisms. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:60a9fcc7-b939-4075-be31-ed69014ad898 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664774


University of Oxford

8. Honti, Frantisek. A method for the identification of biological pathways.

Degree: PhD, 2014, University of Oxford

 Plenty of gene variants have been associated with disease, indicating widespread genetic heterogeneity, which leaves the molecular basis of complex diseases unclear. However, it is… (more)

Subjects/Keywords: 572.8; Bioinformatics (life sciences); Genetics (life sciences); Genetics (medical sciences); Mathematical genetics and bioinformatics (statistics); genomics; computational biology; gene networks

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APA (6th Edition):

Honti, F. (2014). A method for the identification of biological pathways. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e7079080-a814-431a-badd-35080f5a2825 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692865

Chicago Manual of Style (16th Edition):

Honti, Frantisek. “A method for the identification of biological pathways.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:e7079080-a814-431a-badd-35080f5a2825 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692865.

MLA Handbook (7th Edition):

Honti, Frantisek. “A method for the identification of biological pathways.” 2014. Web. 20 Jan 2020.

Vancouver:

Honti F. A method for the identification of biological pathways. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:e7079080-a814-431a-badd-35080f5a2825 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692865.

Council of Science Editors:

Honti F. A method for the identification of biological pathways. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:e7079080-a814-431a-badd-35080f5a2825 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692865


University of Oxford

9. Allchin, Lorraine Doreen May. Statistical methods for mapping complex traits.

Degree: PhD, 2014, University of Oxford

 The first section of this thesis addresses the problem of simultaneously identifying multiple loci that are associated with a trait, using a Bayesian Markov Chain… (more)

Subjects/Keywords: 519.5; Mathematical genetics and bioinformatics (statistics); Bayesian statistics; Markov chain Monte Carlo

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APA (6th Edition):

Allchin, L. D. M. (2014). Statistical methods for mapping complex traits. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:65f392ba-1b64-4b00-8871-7cee98809ce1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627814

Chicago Manual of Style (16th Edition):

Allchin, Lorraine Doreen May. “Statistical methods for mapping complex traits.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:65f392ba-1b64-4b00-8871-7cee98809ce1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627814.

MLA Handbook (7th Edition):

Allchin, Lorraine Doreen May. “Statistical methods for mapping complex traits.” 2014. Web. 20 Jan 2020.

Vancouver:

Allchin LDM. Statistical methods for mapping complex traits. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:65f392ba-1b64-4b00-8871-7cee98809ce1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627814.

Council of Science Editors:

Allchin LDM. Statistical methods for mapping complex traits. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:65f392ba-1b64-4b00-8871-7cee98809ce1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627814


University of Oxford

10. Barrett, Jeffrey C. Design and analysis of genome-wide association studies.

Degree: 2008, University of Oxford

 Despite many years of effort, linkage and candidate gene association studies have yielded disappointingly few risk loci for common human diseases such as diabetes, auto-immune… (more)

Subjects/Keywords: 616.042; Genetics (life sciences) : Mathematical genetics and bioinformatics (statistics) : genome-wide association study : crohn's disease

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APA (6th Edition):

Barrett, J. C. (2008). Design and analysis of genome-wide association studies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:45790b5c-e50c-406a-bb3c-a96868b11a28 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489410

Chicago Manual of Style (16th Edition):

Barrett, Jeffrey C. “Design and analysis of genome-wide association studies.” 2008. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:45790b5c-e50c-406a-bb3c-a96868b11a28 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489410.

MLA Handbook (7th Edition):

Barrett, Jeffrey C. “Design and analysis of genome-wide association studies.” 2008. Web. 20 Jan 2020.

Vancouver:

Barrett JC. Design and analysis of genome-wide association studies. [Internet] [Doctoral dissertation]. University of Oxford; 2008. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:45790b5c-e50c-406a-bb3c-a96868b11a28 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489410.

Council of Science Editors:

Barrett JC. Design and analysis of genome-wide association studies. [Doctoral Dissertation]. University of Oxford; 2008. Available from: http://ora.ox.ac.uk/objects/uuid:45790b5c-e50c-406a-bb3c-a96868b11a28 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489410


University of Oxford

11. Hechter, Eliana. On genetic variants underlying common disease.

Degree: PhD, 2011, University of Oxford

 Genome-wide association studies (GWAS) exploit the correlation in ge- netic diversity along chromosomes in order to detect effects on disease risk without having to type… (more)

Subjects/Keywords: 616.071; Bioinformatics (life sciences); Genetics (life sciences); Genetics (medical sciences); Computationally-intensive statistics; Mathematical genetics and bioinformatics (statistics); statistical genetics; population genetics; genome-wide association studies

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APA (6th Edition):

Hechter, E. (2011). On genetic variants underlying common disease. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:d883f20e-7dad-4216-8851-b006993832fd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555375

Chicago Manual of Style (16th Edition):

Hechter, Eliana. “On genetic variants underlying common disease.” 2011. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:d883f20e-7dad-4216-8851-b006993832fd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555375.

MLA Handbook (7th Edition):

Hechter, Eliana. “On genetic variants underlying common disease.” 2011. Web. 20 Jan 2020.

Vancouver:

Hechter E. On genetic variants underlying common disease. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:d883f20e-7dad-4216-8851-b006993832fd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555375.

Council of Science Editors:

Hechter E. On genetic variants underlying common disease. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:d883f20e-7dad-4216-8851-b006993832fd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555375


University of Oxford

12. Meader, Stephen. Application of the Neutral Indel Model to genome sequences for diverse metazoans.

Degree: PhD, 2010, University of Oxford

 The Neutral Indel Model is able to predict accurately the distribution of indel events in alignments of neutrally evolving genomic sequence. Here, I apply this… (more)

Subjects/Keywords: 572.8; Bioinformatics (life sciences); Genetics (life sciences); Evolution (zoology); Mathematical genetics and bioinformatics (statistics); genomics; evolution; constraint; Indel; metazoan

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APA (6th Edition):

Meader, S. (2010). Application of the Neutral Indel Model to genome sequences for diverse metazoans. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:18f8c5fc-28f2-4d5e-aa87-c1086582213c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540144

Chicago Manual of Style (16th Edition):

Meader, Stephen. “Application of the Neutral Indel Model to genome sequences for diverse metazoans.” 2010. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:18f8c5fc-28f2-4d5e-aa87-c1086582213c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540144.

MLA Handbook (7th Edition):

Meader, Stephen. “Application of the Neutral Indel Model to genome sequences for diverse metazoans.” 2010. Web. 20 Jan 2020.

Vancouver:

Meader S. Application of the Neutral Indel Model to genome sequences for diverse metazoans. [Internet] [Doctoral dissertation]. University of Oxford; 2010. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:18f8c5fc-28f2-4d5e-aa87-c1086582213c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540144.

Council of Science Editors:

Meader S. Application of the Neutral Indel Model to genome sequences for diverse metazoans. [Doctoral Dissertation]. University of Oxford; 2010. Available from: http://ora.ox.ac.uk/objects/uuid:18f8c5fc-28f2-4d5e-aa87-c1086582213c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540144


University of Oxford

13. Ciampa, Julia Grant. Multilocus approaches to the detection of disease susceptibility regions : methods and applications.

Degree: PhD, 2012, University of Oxford

 This thesis focuses on multilocus methods designed to detect single nucleotide polymorphisms (SNPs) that are associated with disease using case-control data. I study multilocus methods… (more)

Subjects/Keywords: 572.8; Statistics (see also social sciences); Mathematical genetics and bioinformatics (statistics); statistical genetics; multilocus analysis; genetic interaction; prostate cancer

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APA (6th Edition):

Ciampa, J. G. (2012). Multilocus approaches to the detection of disease susceptibility regions : methods and applications. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8f82a624-7d80-438c-af3e-68ce983ff45f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580916

Chicago Manual of Style (16th Edition):

Ciampa, Julia Grant. “Multilocus approaches to the detection of disease susceptibility regions : methods and applications.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:8f82a624-7d80-438c-af3e-68ce983ff45f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580916.

MLA Handbook (7th Edition):

Ciampa, Julia Grant. “Multilocus approaches to the detection of disease susceptibility regions : methods and applications.” 2012. Web. 20 Jan 2020.

Vancouver:

Ciampa JG. Multilocus approaches to the detection of disease susceptibility regions : methods and applications. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:8f82a624-7d80-438c-af3e-68ce983ff45f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580916.

Council of Science Editors:

Ciampa JG. Multilocus approaches to the detection of disease susceptibility regions : methods and applications. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:8f82a624-7d80-438c-af3e-68ce983ff45f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580916


University of Oxford

14. Xifara, Dionysia-Kiara. The detection, structure and uses of extended haplotype identity in population genetic data.

Degree: PhD, 2014, University of Oxford

 In large-scale population genomic data sets, individual chromosomes are likely to share extended regions of haplotype identity with others in the sample. Patterns of local… (more)

Subjects/Keywords: 576.5; Mathematical genetics and bioinformatics (statistics); haplotype estimation; identity by descent; extended haplotype sharing; ancestry

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APA (6th Edition):

Xifara, D. (2014). The detection, structure and uses of extended haplotype identity in population genetic data. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:9fabc91a-dd07-4deb-b722-f6b9110b34fb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680409

Chicago Manual of Style (16th Edition):

Xifara, Dionysia-Kiara. “The detection, structure and uses of extended haplotype identity in population genetic data.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:9fabc91a-dd07-4deb-b722-f6b9110b34fb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680409.

MLA Handbook (7th Edition):

Xifara, Dionysia-Kiara. “The detection, structure and uses of extended haplotype identity in population genetic data.” 2014. Web. 20 Jan 2020.

Vancouver:

Xifara D. The detection, structure and uses of extended haplotype identity in population genetic data. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:9fabc91a-dd07-4deb-b722-f6b9110b34fb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680409.

Council of Science Editors:

Xifara D. The detection, structure and uses of extended haplotype identity in population genetic data. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:9fabc91a-dd07-4deb-b722-f6b9110b34fb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680409


University of Oxford

15. O'Connell, Jared Michael. Statistical methods for genotype microarray data on large cohorts of individuals.

Degree: PhD, 2014, University of Oxford

 Genotype microarrays assay hundreds of thousands of genetic variants on an individual's genome. The availability of this high throughput genotyping capability has transformed the field… (more)

Subjects/Keywords: 572.8; Mathematical genetics and bioinformatics (statistics); haplotype; microarray; phasing; genotype calling; pedigree; recombination

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APA (6th Edition):

O'Connell, J. M. (2014). Statistical methods for genotype microarray data on large cohorts of individuals. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:4e3328cf-0d8e-4587-b24d-9b59fa220f32 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640029

Chicago Manual of Style (16th Edition):

O'Connell, Jared Michael. “Statistical methods for genotype microarray data on large cohorts of individuals.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:4e3328cf-0d8e-4587-b24d-9b59fa220f32 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640029.

MLA Handbook (7th Edition):

O'Connell, Jared Michael. “Statistical methods for genotype microarray data on large cohorts of individuals.” 2014. Web. 20 Jan 2020.

Vancouver:

O'Connell JM. Statistical methods for genotype microarray data on large cohorts of individuals. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:4e3328cf-0d8e-4587-b24d-9b59fa220f32 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640029.

Council of Science Editors:

O'Connell JM. Statistical methods for genotype microarray data on large cohorts of individuals. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:4e3328cf-0d8e-4587-b24d-9b59fa220f32 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640029


University of Oxford

16. Bhattacharya, Kanishka. Gene x gene interactions in genome wide association studies.

Degree: PhD, 2014, University of Oxford

 Genome wide association studies (GWAS) have revolutionized our approach to mapping genetic determinants of complex human diseases. However, even with success from recent studies, we… (more)

Subjects/Keywords: 572; Genetics (life sciences); Bioinformatics (life sciences); Mathematics; Mathematical biology; Bioinformatics (technology); Mathematical genetics and bioinformatics (statistics); Statistics (see also social sciences); Statistics; Genetics; Bioinformatics; Epistasis; Intrapid; Interaction; Computation; Diabetes; Obesity; Coronary Heart Disease; Crohn's disease; Inflammatory bowel disease; Hypertension; Rheumatoid arthritis

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APA (6th Edition):

Bhattacharya, K. (2014). Gene x gene interactions in genome wide association studies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:6cb7ab29-90df-4d70-bc2f-531f874b79d0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640080

Chicago Manual of Style (16th Edition):

Bhattacharya, Kanishka. “Gene x gene interactions in genome wide association studies.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:6cb7ab29-90df-4d70-bc2f-531f874b79d0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640080.

MLA Handbook (7th Edition):

Bhattacharya, Kanishka. “Gene x gene interactions in genome wide association studies.” 2014. Web. 20 Jan 2020.

Vancouver:

Bhattacharya K. Gene x gene interactions in genome wide association studies. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:6cb7ab29-90df-4d70-bc2f-531f874b79d0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640080.

Council of Science Editors:

Bhattacharya K. Gene x gene interactions in genome wide association studies. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:6cb7ab29-90df-4d70-bc2f-531f874b79d0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640080


University of Oxford

17. Saadi, Habib. Lambda-Fleming-Viot processes and their spatial extensions.

Degree: PhD, 2011, University of Oxford

 The subject of this thesis is the study of certain stochastic models arising in Population Genetics. The study of biological evolution naturally motivates the construction… (more)

Subjects/Keywords: 519.2; Probability theory and stochastic processes; Mathematical genetics and bioinformatics (statistics); Computationally-intensive statistics; Stochastic processes; Mathematical genetics; Lambda coalescent; Lambda Fleming Viot; Bayesien statistics; genealogies

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APA (6th Edition):

Saadi, H. (2011). Lambda-Fleming-Viot processes and their spatial extensions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:5e069206-e124-4b21-aec2-df7a69393038 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595897

Chicago Manual of Style (16th Edition):

Saadi, Habib. “Lambda-Fleming-Viot processes and their spatial extensions.” 2011. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:5e069206-e124-4b21-aec2-df7a69393038 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595897.

MLA Handbook (7th Edition):

Saadi, Habib. “Lambda-Fleming-Viot processes and their spatial extensions.” 2011. Web. 20 Jan 2020.

Vancouver:

Saadi H. Lambda-Fleming-Viot processes and their spatial extensions. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:5e069206-e124-4b21-aec2-df7a69393038 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595897.

Council of Science Editors:

Saadi H. Lambda-Fleming-Viot processes and their spatial extensions. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:5e069206-e124-4b21-aec2-df7a69393038 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595897


University of Oxford

18. Wendler, Jason Patrick. Accessing complex genomic variation in Plasmodium falciparum natural infections.

Degree: PhD, 2015, University of Oxford

 Genetic polymorphism in Plasmodium falciparum is a considerable obstacle to malaria intervention. Parasites have repeatedly evolved to overcome every front-line antimalarial deployed throughout history, and… (more)

Subjects/Keywords: 616.9; Medical Sciences; Infectious diseases; Biology (medical sciences); Genetics (medical sciences); Malaria; Mathematical genetics and bioinformatics (statistics); Bioinformatics (technology); genomics; bioinformatics; computational biology; drug resistance

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APA (6th Edition):

Wendler, J. P. (2015). Accessing complex genomic variation in Plasmodium falciparum natural infections. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:c9f1ea37-7005-4757-a869-7eba82406a26 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667035

Chicago Manual of Style (16th Edition):

Wendler, Jason Patrick. “Accessing complex genomic variation in Plasmodium falciparum natural infections.” 2015. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:c9f1ea37-7005-4757-a869-7eba82406a26 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667035.

MLA Handbook (7th Edition):

Wendler, Jason Patrick. “Accessing complex genomic variation in Plasmodium falciparum natural infections.” 2015. Web. 20 Jan 2020.

Vancouver:

Wendler JP. Accessing complex genomic variation in Plasmodium falciparum natural infections. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:c9f1ea37-7005-4757-a869-7eba82406a26 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667035.

Council of Science Editors:

Wendler JP. Accessing complex genomic variation in Plasmodium falciparum natural infections. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:c9f1ea37-7005-4757-a869-7eba82406a26 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667035


University of Oxford

19. Loizides, Charalambos. Extensions of the case-control design in genome-wide association studies.

Degree: 2012, University of Oxford

 The case-control design is one of the most commonly used designs in genome- wide asociation studies. When we increase the sample size of either the… (more)

Subjects/Keywords: 519.537; Mathematical genetics and bioinformatics (statistics) : Statistics (see also social sciences) : genome-wide association studies : gwas : association tests

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APA (6th Edition):

Loizides, C. (2012). Extensions of the case-control design in genome-wide association studies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:89e057e5-d30f-4125-b210-14d1f2aa37c1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560931

Chicago Manual of Style (16th Edition):

Loizides, Charalambos. “Extensions of the case-control design in genome-wide association studies.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:89e057e5-d30f-4125-b210-14d1f2aa37c1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560931.

MLA Handbook (7th Edition):

Loizides, Charalambos. “Extensions of the case-control design in genome-wide association studies.” 2012. Web. 20 Jan 2020.

Vancouver:

Loizides C. Extensions of the case-control design in genome-wide association studies. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:89e057e5-d30f-4125-b210-14d1f2aa37c1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560931.

Council of Science Editors:

Loizides C. Extensions of the case-control design in genome-wide association studies. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:89e057e5-d30f-4125-b210-14d1f2aa37c1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560931


University of Oxford

20. Hosseini, Mona. Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq.

Degree: PhD, 2013, University of Oxford

 Variation at regulatory elements, identified through hypersensitivity to digestion by Deoxyribonuclease I (DNase I), is believed to contribute to variation in complex traits, but the… (more)

Subjects/Keywords: 616.027; Medical Sciences; Genetics (medical sciences); Mathematical genetics and bioinformatics (statistics); DNaseI hypersensitive sites; DNase-seq; inbred mice; chromatin variation

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APA (6th Edition):

Hosseini, M. (2013). Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:c76109fc-93b5-4e0b-b7df-0277cbf527a9 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581372

Chicago Manual of Style (16th Edition):

Hosseini, Mona. “Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:c76109fc-93b5-4e0b-b7df-0277cbf527a9 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581372.

MLA Handbook (7th Edition):

Hosseini, Mona. “Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq.” 2013. Web. 20 Jan 2020.

Vancouver:

Hosseini M. Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:c76109fc-93b5-4e0b-b7df-0277cbf527a9 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581372.

Council of Science Editors:

Hosseini M. Genome-wide DNaseI hypersensitive sites profiles in laboratory mouse strains by DNase-seq. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:c76109fc-93b5-4e0b-b7df-0277cbf527a9 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581372


University of California – San Francisco

21. Park, Danny. New Computational Approaches for Analyzing Admixed Populations.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2017, University of California – San Francisco

 This work revolves around developing, applying, and evaluating computational methods for the analysis of genomic datasets of recently admixed populations. Individuals from recently admixed populations,… (more)

Subjects/Keywords: Genetics; Bioinformatics; Statistics; Admixture; Statistical Genetics

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APA (6th Edition):

Park, D. (2017). New Computational Approaches for Analyzing Admixed Populations. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/8m15v4pk

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):

Park, Danny. “New Computational Approaches for Analyzing Admixed Populations.” 2017. Thesis, University of California – San Francisco. Accessed January 20, 2020. http://www.escholarship.org/uc/item/8m15v4pk.

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

MLA Handbook (7th Edition):

Park, Danny. “New Computational Approaches for Analyzing Admixed Populations.” 2017. Web. 20 Jan 2020.

Vancouver:

Park D. New Computational Approaches for Analyzing Admixed Populations. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2020 Jan 20]. Available from: http://www.escholarship.org/uc/item/8m15v4pk.

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

Council of Science Editors:

Park D. New Computational Approaches for Analyzing Admixed Populations. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/8m15v4pk

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


University of Oxford

22. Rosmarin, Daniel Norris. Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer.

Degree: PhD, 2013, University of Oxford

 Despite a decade of publications investigating the effect of germline polymorphisms on both toxicity related to treatment with 5-fluorouracil-based (5-FU) chemotherapy and prognosis following diagnosis… (more)

Subjects/Keywords: 616.99; Mathematical biology; Medical Sciences; Clinical genetics; Gene medicine; Biology (medical sciences); Genetics (medical sciences); Gastroenterology; Oncology; Pharmacology; Enzymes; Molecular genetics; Mathematical genetics and bioinformatics (statistics); Computationally-intensive statistics; Bioinformatics (technology); Bioinformatics (biochemistry); Bioinformatics (life sciences); Biology; Genetics (life sciences); Metabolism; 5-fluorouracil; cancer; colorectal cancer; toxicity; survival; toxgnostics; genetics; drug personalisation; drug personalization; diarrhoea; association study; chemotherapy; neutropaenia; thrombocytopaenia

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APA (6th Edition):

Rosmarin, D. N. (2013). Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:d5e2c306-689c-4c53-b4c3-2c1001b04ec6 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618394

Chicago Manual of Style (16th Edition):

Rosmarin, Daniel Norris. “Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:d5e2c306-689c-4c53-b4c3-2c1001b04ec6 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618394.

MLA Handbook (7th Edition):

Rosmarin, Daniel Norris. “Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer.” 2013. Web. 20 Jan 2020.

Vancouver:

Rosmarin DN. Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:d5e2c306-689c-4c53-b4c3-2c1001b04ec6 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618394.

Council of Science Editors:

Rosmarin DN. Germline determinants of 5-fluorouracil drug toxicity and patient survival in colorectal cancer. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:d5e2c306-689c-4c53-b4c3-2c1001b04ec6 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618394


University of Oxford

23. Iotchkova, Valentina Valentinova. Bayesian methods for multivariate phenotype analysis in genome-wide association studies.

Degree: PhD, 2013, University of Oxford

 Most genome-wide association studies search for genetic variants associated to a single trait of interest, despite the main interest usually being the understanding of a… (more)

Subjects/Keywords: 519.5; Statistics (see also social sciences); Computationally-intensive statistics; Mathematical genetics and bioinformatics (statistics); Applications and algorithms; statistics; method; modelling; genotype; phenotype; bayesian; multivariate

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APA (6th Edition):

Iotchkova, V. V. (2013). Bayesian methods for multivariate phenotype analysis in genome-wide association studies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:66fd61e1-a6e3-4e91-959b-31a3ec88967c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635179

Chicago Manual of Style (16th Edition):

Iotchkova, Valentina Valentinova. “Bayesian methods for multivariate phenotype analysis in genome-wide association studies.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:66fd61e1-a6e3-4e91-959b-31a3ec88967c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635179.

MLA Handbook (7th Edition):

Iotchkova, Valentina Valentinova. “Bayesian methods for multivariate phenotype analysis in genome-wide association studies.” 2013. Web. 20 Jan 2020.

Vancouver:

Iotchkova VV. Bayesian methods for multivariate phenotype analysis in genome-wide association studies. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:66fd61e1-a6e3-4e91-959b-31a3ec88967c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635179.

Council of Science Editors:

Iotchkova VV. Bayesian methods for multivariate phenotype analysis in genome-wide association studies. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:66fd61e1-a6e3-4e91-959b-31a3ec88967c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635179


University of Oxford

24. Krohn, Jonathan Jacob Pastushchyn. Genes contributing to variation in fear-related behaviour.

Degree: PhD, 2013, University of Oxford

 Anxiety and depression are highly prevalent diseases with common heritable elements, but the particular genetic mechanisms and biological pathways underlying them are poorly understood. Part… (more)

Subjects/Keywords: 572.8; Bioinformatics (life sciences); Biology; Genetics (life sciences); Behaviour (zoology); Computer science (mathematics); Mathematical biology; Clinical genetics; Biology (medical sciences); Genetics (medical sciences); Neurogenetics; Anxiety disorders; Emotion research; Molecular neuropathology; Behavioural Neuroscience; Mathematical genetics and bioinformatics (statistics); Computationally-intensive statistics; Bioinformatics (technology); Applications and algorithms; genetics; gene expression; computational statistics; behaviour; emotion; anxiety; Bayesian; frequentist

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APA (6th Edition):

Krohn, J. J. P. (2013). Genes contributing to variation in fear-related behaviour. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:1e8e40bd-9a98-405f-9463-e9423f0a60ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669890

Chicago Manual of Style (16th Edition):

Krohn, Jonathan Jacob Pastushchyn. “Genes contributing to variation in fear-related behaviour.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:1e8e40bd-9a98-405f-9463-e9423f0a60ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669890.

MLA Handbook (7th Edition):

Krohn, Jonathan Jacob Pastushchyn. “Genes contributing to variation in fear-related behaviour.” 2013. Web. 20 Jan 2020.

Vancouver:

Krohn JJP. Genes contributing to variation in fear-related behaviour. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:1e8e40bd-9a98-405f-9463-e9423f0a60ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669890.

Council of Science Editors:

Krohn JJP. Genes contributing to variation in fear-related behaviour. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:1e8e40bd-9a98-405f-9463-e9423f0a60ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669890


University of Oxford

25. Hill, Jamie Richard. Fold recognition and alignment in the 'twilight zone'.

Degree: PhD, 2013, University of Oxford

 At present, the most accurate approach to predicting protein structure, comparative modelling, builds a model of a target sequence using known protein structures as templates.… (more)

Subjects/Keywords: 572; Bioinformatics (biochemistry); Bioinformatics (life sciences); Membrane proteins; Protein folding; Mathematical genetics and bioinformatics (statistics); Membrane protein; protein; twilight zone; fold recognition; comparative modelling; homology; alignment; correlated substitution

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APA (6th Edition):

Hill, J. R. (2013). Fold recognition and alignment in the 'twilight zone'. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946

Chicago Manual of Style (16th Edition):

Hill, Jamie Richard. “Fold recognition and alignment in the 'twilight zone'.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946.

MLA Handbook (7th Edition):

Hill, Jamie Richard. “Fold recognition and alignment in the 'twilight zone'.” 2013. Web. 20 Jan 2020.

Vancouver:

Hill JR. Fold recognition and alignment in the 'twilight zone'. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946.

Council of Science Editors:

Hill JR. Fold recognition and alignment in the 'twilight zone'. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946


University of Oxford

26. Edwards, Hannah Elizabeth. Exploring the fold space preferences of ancient and newborn protein superfamilies.

Degree: PhD, 2014, University of Oxford

 Protein evolution is a complex and diverse process, yielding an incredible assortment of biological functions and pathways occurring in the cells of living organisms. The… (more)

Subjects/Keywords: 572; Mathematical genetics and bioinformatics (statistics); Protein folding; Mathematical biology; Life Sciences; Bioinformatics (life sciences); protein structure; fold space; protein evolution; protein structure classification

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APA (6th Edition):

Edwards, H. E. (2014). Exploring the fold space preferences of ancient and newborn protein superfamilies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:4a619051-db24-4a4c-bdad-61899bc1de03 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658413

Chicago Manual of Style (16th Edition):

Edwards, Hannah Elizabeth. “Exploring the fold space preferences of ancient and newborn protein superfamilies.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:4a619051-db24-4a4c-bdad-61899bc1de03 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658413.

MLA Handbook (7th Edition):

Edwards, Hannah Elizabeth. “Exploring the fold space preferences of ancient and newborn protein superfamilies.” 2014. Web. 20 Jan 2020.

Vancouver:

Edwards HE. Exploring the fold space preferences of ancient and newborn protein superfamilies. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:4a619051-db24-4a4c-bdad-61899bc1de03 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658413.

Council of Science Editors:

Edwards HE. Exploring the fold space preferences of ancient and newborn protein superfamilies. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:4a619051-db24-4a4c-bdad-61899bc1de03 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658413


University of Oxford

27. Repapi, Emmanouela. An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans.

Degree: PhD, 2013, University of Oxford

 The identification of genetic variants such as single nucleotide polymorphisms (SNPs), which affect cancer progression, survival and response to treatments could help in the design… (more)

Subjects/Keywords: 611; Bioinformatics (life sciences); Genetics (life sciences); Mathematical genetics and bioinformatics (statistics); Random Survival Forest; Cancer; Transcription Factor Binding Sites; Survival Analysis

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APA (6th Edition):

Repapi, E. (2013). An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:16f4482e-7f83-46c9-88d9-583c4154e044 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635182

Chicago Manual of Style (16th Edition):

Repapi, Emmanouela. “An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:16f4482e-7f83-46c9-88d9-583c4154e044 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635182.

MLA Handbook (7th Edition):

Repapi, Emmanouela. “An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans.” 2013. Web. 20 Jan 2020.

Vancouver:

Repapi E. An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:16f4482e-7f83-46c9-88d9-583c4154e044 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635182.

Council of Science Editors:

Repapi E. An integrated genomic approach for the identification and analysis of single nucleotide polymorphisms that affect cancer in humans. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:16f4482e-7f83-46c9-88d9-583c4154e044 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635182


University of Oxford

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

Degree: PhD, 2012, University of Oxford

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Pfeifer, Susanne. “Statistical challenges in the detection of mutation and variation using high throughput sequencing.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605.

MLA Handbook (7th Edition):

Pfeifer, Susanne. “Statistical challenges in the detection of mutation and variation using high throughput sequencing.” 2012. Web. 20 Jan 2020.

Vancouver:

Pfeifer S. Statistical challenges in the detection of mutation and variation using high throughput sequencing. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:e49ce2fa-aa2c-42d7-bb54-c63e50d14afb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589605.

Council of Science Editors:

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


University of Oxford

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

Degree: PhD, 2013, University of Oxford

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Venn, Oliver Claude. “Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960.

MLA Handbook (7th Edition):

Venn, Oliver Claude. “Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing.” 2013. Web. 20 Jan 2020.

Vancouver:

Venn OC. Inferring the fine-scale structure and evolution of recombination from high-throughput genome sequencing. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:b74f6706-a37d-4d71-975d-02e0f79ccdf1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595960.

Council of Science Editors:

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


University of Oxford

30. Bhatt, Samir. Statistical analysis of natural selection in RNA virus populations.

Degree: PhD, 2010, University of Oxford

 A key goal of modern evolutionary biology is the identification of genes or genome regions that have been targeted by natural selection. Methods for detecting… (more)

Subjects/Keywords: 572.8; Evolution (zoology); Mathematical genetics and bioinformatics (statistics); evolution; RNA virus; adaptation; influenza; McDonald Kreitman Test; Site Frequency Spectrum

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APA (6th Edition):

Bhatt, S. (2010). Statistical analysis of natural selection in RNA virus populations. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:64341c38-f09e-48ed-84e8-7ab9f171a753 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543055

Chicago Manual of Style (16th Edition):

Bhatt, Samir. “Statistical analysis of natural selection in RNA virus populations.” 2010. Doctoral Dissertation, University of Oxford. Accessed January 20, 2020. http://ora.ox.ac.uk/objects/uuid:64341c38-f09e-48ed-84e8-7ab9f171a753 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543055.

MLA Handbook (7th Edition):

Bhatt, Samir. “Statistical analysis of natural selection in RNA virus populations.” 2010. Web. 20 Jan 2020.

Vancouver:

Bhatt S. Statistical analysis of natural selection in RNA virus populations. [Internet] [Doctoral dissertation]. University of Oxford; 2010. [cited 2020 Jan 20]. Available from: http://ora.ox.ac.uk/objects/uuid:64341c38-f09e-48ed-84e8-7ab9f171a753 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543055.

Council of Science Editors:

Bhatt S. Statistical analysis of natural selection in RNA virus populations. [Doctoral Dissertation]. University of Oxford; 2010. Available from: http://ora.ox.ac.uk/objects/uuid:64341c38-f09e-48ed-84e8-7ab9f171a753 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543055

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