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You searched for subject:(Copy number variation). Showing records 1 – 30 of 141 total matches.

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1. Huang, Ni. The functional impact of copy number variation in the human genome.

Degree: PhD, 2012, University of Cambridge

Copy number variation (CNV) is a class of genetic variation where large segments of the genome vary in copy number among different individuals. It has… (more)

Subjects/Keywords: Human genetics; Copy number variation

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APA (6th Edition):

Huang, N. (2012). The functional impact of copy number variation in the human genome. (Doctoral Dissertation). University of Cambridge. Retrieved from http://www.dspace.cam.ac.uk/handle/1810/242182https://www.repository.cam.ac.uk/bitstream/1810/242182/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/242182/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/242182/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/242182/8/ni.huang.thesis.2011.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/9/ni.huang.thesis.2011.pdf.jpg

Chicago Manual of Style (16th Edition):

Huang, Ni. “The functional impact of copy number variation in the human genome.” 2012. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. http://www.dspace.cam.ac.uk/handle/1810/242182https://www.repository.cam.ac.uk/bitstream/1810/242182/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/242182/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/242182/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/242182/8/ni.huang.thesis.2011.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/9/ni.huang.thesis.2011.pdf.jpg.

MLA Handbook (7th Edition):

Huang, Ni. “The functional impact of copy number variation in the human genome.” 2012. Web. 31 Oct 2020.

Vancouver:

Huang N. The functional impact of copy number variation in the human genome. [Internet] [Doctoral dissertation]. University of Cambridge; 2012. [cited 2020 Oct 31]. Available from: http://www.dspace.cam.ac.uk/handle/1810/242182https://www.repository.cam.ac.uk/bitstream/1810/242182/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/242182/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/242182/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/242182/8/ni.huang.thesis.2011.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/9/ni.huang.thesis.2011.pdf.jpg.

Council of Science Editors:

Huang N. The functional impact of copy number variation in the human genome. [Doctoral Dissertation]. University of Cambridge; 2012. Available from: http://www.dspace.cam.ac.uk/handle/1810/242182https://www.repository.cam.ac.uk/bitstream/1810/242182/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/242182/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/242182/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/242182/8/ni.huang.thesis.2011.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/242182/9/ni.huang.thesis.2011.pdf.jpg


Colorado State University

2. Sedam, Hailey Nicole Conover. Genome instability: a pre-existing condition.

Degree: PhD, Cell and Molecular Biology, 2018, Colorado State University

Copy number variations (CNV), or large amplifications or deletions in the genome, account for about 50% of human genetic diversity. CNVs across genomic regions essential… (more)

Subjects/Keywords: genome instability; copy number variation; Saccharomyces cerevisiae

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APA (6th Edition):

Sedam, H. N. C. (2018). Genome instability: a pre-existing condition. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/191411

Chicago Manual of Style (16th Edition):

Sedam, Hailey Nicole Conover. “Genome instability: a pre-existing condition.” 2018. Doctoral Dissertation, Colorado State University. Accessed October 31, 2020. http://hdl.handle.net/10217/191411.

MLA Handbook (7th Edition):

Sedam, Hailey Nicole Conover. “Genome instability: a pre-existing condition.” 2018. Web. 31 Oct 2020.

Vancouver:

Sedam HNC. Genome instability: a pre-existing condition. [Internet] [Doctoral dissertation]. Colorado State University; 2018. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10217/191411.

Council of Science Editors:

Sedam HNC. Genome instability: a pre-existing condition. [Doctoral Dissertation]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/191411


University of Saskatchewan

3. Mirabzadeh-Ardakani, Ali. Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle.

Degree: 2016, University of Saskatchewan

 The DEFB103 gene is a member of the β-defensin gene family, and it has not been well studied in cattle. In this study DEFB103 gene… (more)

Subjects/Keywords: Copy number variation; Defensin; Haplotype; Splicing

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APA (6th Edition):

Mirabzadeh-Ardakani, A. (2016). Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7277

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):

Mirabzadeh-Ardakani, Ali. “Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle.” 2016. Thesis, University of Saskatchewan. Accessed October 31, 2020. http://hdl.handle.net/10388/7277.

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

MLA Handbook (7th Edition):

Mirabzadeh-Ardakani, Ali. “Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle.” 2016. Web. 31 Oct 2020.

Vancouver:

Mirabzadeh-Ardakani A. Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10388/7277.

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

Council of Science Editors:

Mirabzadeh-Ardakani A. Characterization of DEFB103 gene structure, gene expression and its haplotype association with three common diseases in Beef and Holstein cattle. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7277

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


University of Iowa

4. Rudd, Danielle Song. Genomic copy number variation in schizophrenia.

Degree: PhD, Genetics, 2014, University of Iowa

  Schizophrenia (OMIM 181500) is an incurable and severe psychiatric disorder comprised of three symptom domains (positive symptoms, negative symptoms and cognitive impairments) with a… (more)

Subjects/Keywords: Copy number variation; Genetics; Psychiatry; Schizophrenia; Genetics

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APA (6th Edition):

Rudd, D. S. (2014). Genomic copy number variation in schizophrenia. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4739

Chicago Manual of Style (16th Edition):

Rudd, Danielle Song. “Genomic copy number variation in schizophrenia.” 2014. Doctoral Dissertation, University of Iowa. Accessed October 31, 2020. https://ir.uiowa.edu/etd/4739.

MLA Handbook (7th Edition):

Rudd, Danielle Song. “Genomic copy number variation in schizophrenia.” 2014. Web. 31 Oct 2020.

Vancouver:

Rudd DS. Genomic copy number variation in schizophrenia. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2020 Oct 31]. Available from: https://ir.uiowa.edu/etd/4739.

Council of Science Editors:

Rudd DS. Genomic copy number variation in schizophrenia. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4739


University of Cambridge

5. Huang, Ni. The functional impact of copy number variation in the human genome.

Degree: PhD, 2012, University of Cambridge

Copy number variation (CNV) is a class of genetic variation where large segments of the genome vary in copy number among different individuals. It has… (more)

Subjects/Keywords: 612; Human genetics; Copy number variation

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

APA (6th Edition):

Huang, N. (2012). The functional impact of copy number variation in the human genome. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.16350 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549226

Chicago Manual of Style (16th Edition):

Huang, Ni. “The functional impact of copy number variation in the human genome.” 2012. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://doi.org/10.17863/CAM.16350 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549226.

MLA Handbook (7th Edition):

Huang, Ni. “The functional impact of copy number variation in the human genome.” 2012. Web. 31 Oct 2020.

Vancouver:

Huang N. The functional impact of copy number variation in the human genome. [Internet] [Doctoral dissertation]. University of Cambridge; 2012. [cited 2020 Oct 31]. Available from: https://doi.org/10.17863/CAM.16350 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549226.

Council of Science Editors:

Huang N. The functional impact of copy number variation in the human genome. [Doctoral Dissertation]. University of Cambridge; 2012. Available from: https://doi.org/10.17863/CAM.16350 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549226


University of Notre Dame

6. Becky Akiko Miller. Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>.

Degree: Biological Sciences, 2012, University of Notre Dame

  There are an estimated 216 million cases of malaria worldwide resulting in 655,000 deaths. Plasmodium falciparum is the intracellular parasite responsible for the 91%… (more)

Subjects/Keywords: copy number variation; array design; population genomics; copy number polymorphism; population genetics

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APA (6th Edition):

Miller, B. A. (2012). Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/2b88qc00f6p

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):

Miller, Becky Akiko. “Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>.” 2012. Thesis, University of Notre Dame. Accessed October 31, 2020. https://curate.nd.edu/show/2b88qc00f6p.

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

MLA Handbook (7th Edition):

Miller, Becky Akiko. “Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>.” 2012. Web. 31 Oct 2020.

Vancouver:

Miller BA. Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>. [Internet] [Thesis]. University of Notre Dame; 2012. [cited 2020 Oct 31]. Available from: https://curate.nd.edu/show/2b88qc00f6p.

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

Council of Science Editors:

Miller BA. Detection and biological assessment of genome structural variation in Plasmodium falciparum</h1>. [Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/2b88qc00f6p

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


University of Guelph

7. Oluwole, Olutobi A. Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls.

Degree: PhD, Department of Biomedical Sciences, 2016, University of Guelph

Copy number variation has been reported in health and disease conditions. Several genes in the genome of both humans and animals exhibit copy number variation(more)

Subjects/Keywords: Genome variation; Copy number variation; TSPY; Aging; Bulls

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APA (6th Edition):

Oluwole, O. A. (2016). Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls. (Doctoral Dissertation). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9685

Chicago Manual of Style (16th Edition):

Oluwole, Olutobi A. “Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls.” 2016. Doctoral Dissertation, University of Guelph. Accessed October 31, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9685.

MLA Handbook (7th Edition):

Oluwole, Olutobi A. “Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls.” 2016. Web. 31 Oct 2020.

Vancouver:

Oluwole OA. Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls. [Internet] [Doctoral dissertation]. University of Guelph; 2016. [cited 2020 Oct 31]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9685.

Council of Science Editors:

Oluwole OA. Testis Specific Protein Y Encoded and Genome Wide Copy Number Variation and Changes in Individual Bulls. [Doctoral Dissertation]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9685


Boston College

8. Wu, Jiantao. Structual variation detection in the human genome.

Degree: PhD, Biology, 2013, Boston College

 Structural variations (SVs), like single nucleotide polymorphisms (SNPs) and short insertion-deletion polymorphisms (INDELs), are a ubiquitous feature of genomic sequences and are major contributors to… (more)

Subjects/Keywords: copy number variation; mobile element insertion; structural variation

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APA (6th Edition):

Wu, J. (2013). Structual variation detection in the human genome. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101332

Chicago Manual of Style (16th Edition):

Wu, Jiantao. “Structual variation detection in the human genome.” 2013. Doctoral Dissertation, Boston College. Accessed October 31, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101332.

MLA Handbook (7th Edition):

Wu, Jiantao. “Structual variation detection in the human genome.” 2013. Web. 31 Oct 2020.

Vancouver:

Wu J. Structual variation detection in the human genome. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2020 Oct 31]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101332.

Council of Science Editors:

Wu J. Structual variation detection in the human genome. [Doctoral Dissertation]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101332


University of Alberta

9. Khorshidi, Azam. Study of the molecular cause of anophthalmia in a consanguineous pedigree.

Degree: MS, Medical Sciences-Medical Genetics, 2012, University of Alberta

 Anophthalmia is a genetically heterogeneous congenital disorder. By using homozygosity mapping in six individuals with anophthalmia from a consanguineous family, five homozygous regions more than… (more)

Subjects/Keywords: Homozygosity mapping; Anophthalmia; Copy number variation; Next generation sequencing

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APA (6th Edition):

Khorshidi, A. (2012). Study of the molecular cause of anophthalmia in a consanguineous pedigree. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/765372006

Chicago Manual of Style (16th Edition):

Khorshidi, Azam. “Study of the molecular cause of anophthalmia in a consanguineous pedigree.” 2012. Masters Thesis, University of Alberta. Accessed October 31, 2020. https://era.library.ualberta.ca/files/765372006.

MLA Handbook (7th Edition):

Khorshidi, Azam. “Study of the molecular cause of anophthalmia in a consanguineous pedigree.” 2012. Web. 31 Oct 2020.

Vancouver:

Khorshidi A. Study of the molecular cause of anophthalmia in a consanguineous pedigree. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Oct 31]. Available from: https://era.library.ualberta.ca/files/765372006.

Council of Science Editors:

Khorshidi A. Study of the molecular cause of anophthalmia in a consanguineous pedigree. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/765372006


University of Guelph

10. Quach, Anh. INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY.

Degree: PhD, Department of Biomedical Sciences, 2015, University of Guelph

 Boars can greatly affect the reproductive success of a herd, especially with the current widespread use of artificial insemination (AI). Low fertility boars in AI… (more)

Subjects/Keywords: Chromosome abnormality; Copy number variation; TSPY; boar fertility

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APA (6th Edition):

Quach, A. (2015). INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY. (Doctoral Dissertation). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9269

Chicago Manual of Style (16th Edition):

Quach, Anh. “INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY.” 2015. Doctoral Dissertation, University of Guelph. Accessed October 31, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9269.

MLA Handbook (7th Edition):

Quach, Anh. “INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY.” 2015. Web. 31 Oct 2020.

Vancouver:

Quach A. INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY. [Internet] [Doctoral dissertation]. University of Guelph; 2015. [cited 2020 Oct 31]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9269.

Council of Science Editors:

Quach A. INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY. [Doctoral Dissertation]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9269


University of Notre Dame

11. Sajeewani Upeka Samarakoon. Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>.

Degree: Biological Sciences, 2012, University of Notre Dame

  Malaria is a devastating infectious disease that has caused death and debilitation for centuries. It remains a globally significant disease despite relentless efforts to… (more)

Subjects/Keywords: copy number variation; recombination; plasmodium falciparum; linkage; malaria

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APA (6th Edition):

Samarakoon, S. U. (2012). Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/b8515m62s7p

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):

Samarakoon, Sajeewani Upeka. “Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>.” 2012. Thesis, University of Notre Dame. Accessed October 31, 2020. https://curate.nd.edu/show/b8515m62s7p.

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

MLA Handbook (7th Edition):

Samarakoon, Sajeewani Upeka. “Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>.” 2012. Web. 31 Oct 2020.

Vancouver:

Samarakoon SU. Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>. [Internet] [Thesis]. University of Notre Dame; 2012. [cited 2020 Oct 31]. Available from: https://curate.nd.edu/show/b8515m62s7p.

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

Council of Science Editors:

Samarakoon SU. Role of recombination in genetic linkage and genome variation in the human malaria parasite, Plasmodium falciparum</h1>. [Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/b8515m62s7p

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


University of Western Ontario

12. Wishart, Andrea E. Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus.

Degree: 2014, University of Western Ontario

Copy number variants (CNVs) are a source of genomic variation associated with altered phenotypes. Somatic copy number mosaicism results when different populations of cells in… (more)

Subjects/Keywords: copy number variation; Mus musculus; somatic mosaicism; spleen; liver; cerebellum; Genomics

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APA (6th Edition):

Wishart, A. E. (2014). Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1997

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):

Wishart, Andrea E. “Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus.” 2014. Thesis, University of Western Ontario. Accessed October 31, 2020. https://ir.lib.uwo.ca/etd/1997.

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

MLA Handbook (7th Edition):

Wishart, Andrea E. “Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus.” 2014. Web. 31 Oct 2020.

Vancouver:

Wishart AE. Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2020 Oct 31]. Available from: https://ir.lib.uwo.ca/etd/1997.

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

Council of Science Editors:

Wishart AE. Somatic Copy Number Mosaicism Contributes to Genomic Diversity in Mus musculus. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/1997

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

13. Lionel, Christopher Anath. Copy Number Variation in Neurodevelopmental Disorders.

Degree: PhD, 2014, University of Toronto

 Recent research on genetic etiologies of different neurodevelopmental conditions such as Autism Spectrum Disorder (ASD), Attention Deficit Hyperactivity Disorder (ADHD) and schizophrenia has highlighted a… (more)

Subjects/Keywords: ADHD; Autism; CNVs; Copy Number Variation; Microarrays; Schizophrenia; 0369

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APA (6th Edition):

Lionel, C. A. (2014). Copy Number Variation in Neurodevelopmental Disorders. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68128

Chicago Manual of Style (16th Edition):

Lionel, Christopher Anath. “Copy Number Variation in Neurodevelopmental Disorders.” 2014. Doctoral Dissertation, University of Toronto. Accessed October 31, 2020. http://hdl.handle.net/1807/68128.

MLA Handbook (7th Edition):

Lionel, Christopher Anath. “Copy Number Variation in Neurodevelopmental Disorders.” 2014. Web. 31 Oct 2020.

Vancouver:

Lionel CA. Copy Number Variation in Neurodevelopmental Disorders. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1807/68128.

Council of Science Editors:

Lionel CA. Copy Number Variation in Neurodevelopmental Disorders. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68128


University of Toronto

14. Lowther, Chelsea Lea Grace. Rare copy number variations associated with schizophrenia and intellectual disability.

Degree: PhD, 2018, University of Toronto

 Schizophrenia is a severe psychiatric disorder associated with significant impairments in cognitive functioning. Extensive evidence supports the importance of genetic aetiology, similar to other neurodevelopmental… (more)

Subjects/Keywords: 22q11.2; Cognitive; Copy number variation; Intellectual disability; NRXN1; Schizophrenia; 0369

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APA (6th Edition):

Lowther, C. L. G. (2018). Rare copy number variations associated with schizophrenia and intellectual disability. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/82962

Chicago Manual of Style (16th Edition):

Lowther, Chelsea Lea Grace. “Rare copy number variations associated with schizophrenia and intellectual disability.” 2018. Doctoral Dissertation, University of Toronto. Accessed October 31, 2020. http://hdl.handle.net/1807/82962.

MLA Handbook (7th Edition):

Lowther, Chelsea Lea Grace. “Rare copy number variations associated with schizophrenia and intellectual disability.” 2018. Web. 31 Oct 2020.

Vancouver:

Lowther CLG. Rare copy number variations associated with schizophrenia and intellectual disability. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1807/82962.

Council of Science Editors:

Lowther CLG. Rare copy number variations associated with schizophrenia and intellectual disability. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/82962


University of Minnesota

15. Lofgren, Lotus. Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems.

Degree: PhD, Plant and Microbial Biology, 2019, University of Minnesota

 Across both wild and human-structured ecosystems, fungi interact with every plant species on earth. From mycorrhizal mutualisms, harmless endophytes, and deadly pathogens, the results of… (more)

Subjects/Keywords: bioinformatics; copy number variation; Genomics; host specificity; Mycology; Suillus

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

APA (6th Edition):

Lofgren, L. (2019). Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/209102

Chicago Manual of Style (16th Edition):

Lofgren, Lotus. “Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems.” 2019. Doctoral Dissertation, University of Minnesota. Accessed October 31, 2020. http://hdl.handle.net/11299/209102.

MLA Handbook (7th Edition):

Lofgren, Lotus. “Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems.” 2019. Web. 31 Oct 2020.

Vancouver:

Lofgren L. Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11299/209102.

Council of Science Editors:

Lofgren L. Reciprocal Informants: Using Fungal Bioinformatics, Genomics, and Ecology to tie Mechanisms to Ecosystems. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/209102


University of Minnesota

16. Zhang, Huanan. Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods.

Degree: PhD, Computer Science, 2017, University of Minnesota

 Because of disease progression and heterogeneity in samples and single cells, biomarker detection among subgroups is important as it provides better understanding on population genetics… (more)

Subjects/Keywords: Copy Number Variation; Latent features; Machine Learning; Transfer Learning

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APA (6th Edition):

Zhang, H. (2017). Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/190520

Chicago Manual of Style (16th Edition):

Zhang, Huanan. “Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods.” 2017. Doctoral Dissertation, University of Minnesota. Accessed October 31, 2020. http://hdl.handle.net/11299/190520.

MLA Handbook (7th Edition):

Zhang, Huanan. “Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods.” 2017. Web. 31 Oct 2020.

Vancouver:

Zhang H. Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11299/190520.

Council of Science Editors:

Zhang H. Detecting Biomarkers among Subgroups with Structured Latent Features and Multitask Learning Methods. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/190520


University of Cambridge

17. Zylstra, Andre. Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae.

Degree: PhD, 2019, University of Cambridge

 Ribosomal DNA (rDNA) forms the template for mature ribosomal RNA (rRNA) and shows considerable sequence conservation through evolution. In eukaryotic genomes rDNA is present in… (more)

Subjects/Keywords: ribosomal DNA; copy number variation; caenorhabditis elegans; saccharomyces cerevisiae; ageing

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APA (6th Edition):

Zylstra, A. (2019). Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.54058 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810077

Chicago Manual of Style (16th Edition):

Zylstra, Andre. “Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://doi.org/10.17863/CAM.54058 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810077.

MLA Handbook (7th Edition):

Zylstra, Andre. “Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae.” 2019. Web. 31 Oct 2020.

Vancouver:

Zylstra A. Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 31]. Available from: https://doi.org/10.17863/CAM.54058 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810077.

Council of Science Editors:

Zylstra A. Phenotypic and transcriptomic consequences of ribosomal DNA copy number variation in Caenorhabditis elegans and Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.54058 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.810077


University of Pennsylvania

18. Tsai, Ellen. Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia.

Degree: 2013, University of Pennsylvania

 The biliary system facilitates transport of bile from the liver, where it is produced, to the gall bladder, where it is stored and later released… (more)

Subjects/Keywords: copy number variation; exome sequencing; genome-wide association study; Bioinformatics; Genetics

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APA (6th Edition):

Tsai, E. (2013). Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/932

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):

Tsai, Ellen. “Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia.” 2013. Thesis, University of Pennsylvania. Accessed October 31, 2020. https://repository.upenn.edu/edissertations/932.

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

MLA Handbook (7th Edition):

Tsai, Ellen. “Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia.” 2013. Web. 31 Oct 2020.

Vancouver:

Tsai E. Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2020 Oct 31]. Available from: https://repository.upenn.edu/edissertations/932.

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

Council of Science Editors:

Tsai E. Genomic Approaches to Understanding Variable Expressivity in Alagille Syndrome and Genetic Susceptibility to Biliary Atresia. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/932

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


University of Melbourne

19. Gaire, Raj Kumar. Effective integration of diverse biological datasets for better understanding of cancer.

Degree: 2012, University of Melbourne

 Cancer is a disease of malfunctioning cells. Nowadays, experiments in cancer research have been producing a large number of datasets that contain measurements of various… (more)

Subjects/Keywords: bioinformatics; cancer; data integration; MIRAGAA; BioNet; miRNA; copy number variation

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APA (6th Edition):

Gaire, R. K. (2012). Effective integration of diverse biological datasets for better understanding of cancer. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37430

Chicago Manual of Style (16th Edition):

Gaire, Raj Kumar. “Effective integration of diverse biological datasets for better understanding of cancer.” 2012. Doctoral Dissertation, University of Melbourne. Accessed October 31, 2020. http://hdl.handle.net/11343/37430.

MLA Handbook (7th Edition):

Gaire, Raj Kumar. “Effective integration of diverse biological datasets for better understanding of cancer.” 2012. Web. 31 Oct 2020.

Vancouver:

Gaire RK. Effective integration of diverse biological datasets for better understanding of cancer. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11343/37430.

Council of Science Editors:

Gaire RK. Effective integration of diverse biological datasets for better understanding of cancer. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37430


University of Cincinnati

20. Cowan, Jason R. The Genetics of Heterotaxy Syndrome.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2015, University of Cincinnati

 Congenital heart defects (CHDs) are the greatest cause of infant morbidity and mortality worldwide, occurring in roughly 8 per 1000 live births (~1%). Heterotaxy, a… (more)

Subjects/Keywords: Genetics; heterotaxy; PFKP; ZIC3; left-right patterning; genetics; copy number variation

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APA (6th Edition):

Cowan, J. R. (2015). The Genetics of Heterotaxy Syndrome. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447689122

Chicago Manual of Style (16th Edition):

Cowan, Jason R. “The Genetics of Heterotaxy Syndrome.” 2015. Doctoral Dissertation, University of Cincinnati. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447689122.

MLA Handbook (7th Edition):

Cowan, Jason R. “The Genetics of Heterotaxy Syndrome.” 2015. Web. 31 Oct 2020.

Vancouver:

Cowan JR. The Genetics of Heterotaxy Syndrome. [Internet] [Doctoral dissertation]. University of Cincinnati; 2015. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447689122.

Council of Science Editors:

Cowan JR. The Genetics of Heterotaxy Syndrome. [Doctoral Dissertation]. University of Cincinnati; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447689122


University of Western Ontario

21. Haghshenas, Ehsan. New algorithms for structural variation detection by de novo genome assembly.

Degree: 2013, University of Western Ontario

 Structural variations (SVs) are changes in the human genome that are reported in several studies to be associated with some diseases. Therefore, designing methods to… (more)

Subjects/Keywords: structural variation; copy number variation; de novo assembly; next-generation sequencing; Other Computer Sciences

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APA (6th Edition):

Haghshenas, E. (2013). New algorithms for structural variation detection by de novo genome assembly. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1832

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):

Haghshenas, Ehsan. “New algorithms for structural variation detection by de novo genome assembly.” 2013. Thesis, University of Western Ontario. Accessed October 31, 2020. https://ir.lib.uwo.ca/etd/1832.

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

MLA Handbook (7th Edition):

Haghshenas, Ehsan. “New algorithms for structural variation detection by de novo genome assembly.” 2013. Web. 31 Oct 2020.

Vancouver:

Haghshenas E. New algorithms for structural variation detection by de novo genome assembly. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2020 Oct 31]. Available from: https://ir.lib.uwo.ca/etd/1832.

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

Council of Science Editors:

Haghshenas E. New algorithms for structural variation detection by de novo genome assembly. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1832

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


University of Helsinki

22. Hakala, Kalle. Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa.

Degree: Department of Clinical Production Animal Medicine; Helsingin yliopisto, Eläinlääketieteellinen tiedekunta, Kliinisen tuotantoeläinlääketieteen osasto; Helsingfors universitet, Veterinärmedicinska fakulteten, Avdelningen för klinisk produktionsdjursmedicin, 2012, University of Helsinki

 Tämän lisensiaatintutkielman tavoitteena on selvittää pohjoissuomenkarjan naudoilla esiintyvän gonadien hypoplasian eli sukurauhasten vajaakehittyneisyyden syitä. Sukurauhasten vajaakehittyneisyyden tiedetään johtuvan itusolujen puutteesta sukurauhasissa. Itusolujen puutos on havaittavissa… (more)

Subjects/Keywords: Gonadihypoplasia; ektooppinen KIT; KIT; KIT copy number variation; Kotieläinten lisääntymistiede; Husdjurens reproduktion; Reproduction of Domestic Animals; Gonadihypoplasia; ektooppinen KIT; KIT; KIT copy number variation

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APA (6th Edition):

Hakala, K. (2012). Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/37673

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):

Hakala, Kalle. “Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa.” 2012. Thesis, University of Helsinki. Accessed October 31, 2020. http://hdl.handle.net/10138/37673.

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

MLA Handbook (7th Edition):

Hakala, Kalle. “Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa.” 2012. Web. 31 Oct 2020.

Vancouver:

Hakala K. Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa. [Internet] [Thesis]. University of Helsinki; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10138/37673.

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

Council of Science Editors:

Hakala K. Gonadihypoplasia lapinlehmillä Ruotsissa ja Suomessa. [Thesis]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/37673

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


University of Iowa

23. Meyer, Kacie Jo. Detection, interpretation, and functional consequences of genomic copy number variation in human disease.

Degree: PhD, Genetics, 2011, University of Iowa

  In recent years, microarray technology has revealed the widespread presence of submicroscopic deletions and duplications throughout the human genome termed copy number variants (CNVs).… (more)

Subjects/Keywords: Age-related macular degeneration; Autism; Bardet-Biedl Syndrome; Clubfoot; Copy number variation; Glaucoma; Genetics

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APA (6th Edition):

Meyer, K. J. (2011). Detection, interpretation, and functional consequences of genomic copy number variation in human disease. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1026

Chicago Manual of Style (16th Edition):

Meyer, Kacie Jo. “Detection, interpretation, and functional consequences of genomic copy number variation in human disease.” 2011. Doctoral Dissertation, University of Iowa. Accessed October 31, 2020. https://ir.uiowa.edu/etd/1026.

MLA Handbook (7th Edition):

Meyer, Kacie Jo. “Detection, interpretation, and functional consequences of genomic copy number variation in human disease.” 2011. Web. 31 Oct 2020.

Vancouver:

Meyer KJ. Detection, interpretation, and functional consequences of genomic copy number variation in human disease. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2020 Oct 31]. Available from: https://ir.uiowa.edu/etd/1026.

Council of Science Editors:

Meyer KJ. Detection, interpretation, and functional consequences of genomic copy number variation in human disease. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/1026

24. Passos, Joana. Implications of histone H2AX abundance in breast cancer.

Degree: 2020, NUI Galway

Histones are responsible for the packaging of DNA into a eukaryotic cell nucleus, and the H2A variant H2AX plays an important role in the DNA… (more)

Subjects/Keywords: breast cancer; H2AX; copy number variation; DNA damage response; DNA double strand breaks; Medicine; Anatomy

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APA (6th Edition):

Passos, J. (2020). Implications of histone H2AX abundance in breast cancer. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/15784

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):

Passos, Joana. “Implications of histone H2AX abundance in breast cancer.” 2020. Thesis, NUI Galway. Accessed October 31, 2020. http://hdl.handle.net/10379/15784.

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

MLA Handbook (7th Edition):

Passos, Joana. “Implications of histone H2AX abundance in breast cancer.” 2020. Web. 31 Oct 2020.

Vancouver:

Passos J. Implications of histone H2AX abundance in breast cancer. [Internet] [Thesis]. NUI Galway; 2020. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10379/15784.

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

Council of Science Editors:

Passos J. Implications of histone H2AX abundance in breast cancer. [Thesis]. NUI Galway; 2020. Available from: http://hdl.handle.net/10379/15784

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


University of Melbourne

25. CANTSILIERIS, STUART. Investigation and assessment of copy number variation in Age-related Macular Degeneration.

Degree: 2013, University of Melbourne

 Age-related Macular Degeneration (AMD) is a common form of irreversible vision loss in Western populations. AMD is classified as a complex multi-factorial disease and is… (more)

Subjects/Keywords: Age-related Macular Degeneration; copy number variation; complex disease; multiplex ligation-dependent probe amplification

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APA (6th Edition):

CANTSILIERIS, S. (2013). Investigation and assessment of copy number variation in Age-related Macular Degeneration. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38343

Chicago Manual of Style (16th Edition):

CANTSILIERIS, STUART. “Investigation and assessment of copy number variation in Age-related Macular Degeneration.” 2013. Doctoral Dissertation, University of Melbourne. Accessed October 31, 2020. http://hdl.handle.net/11343/38343.

MLA Handbook (7th Edition):

CANTSILIERIS, STUART. “Investigation and assessment of copy number variation in Age-related Macular Degeneration.” 2013. Web. 31 Oct 2020.

Vancouver:

CANTSILIERIS S. Investigation and assessment of copy number variation in Age-related Macular Degeneration. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11343/38343.

Council of Science Editors:

CANTSILIERIS S. Investigation and assessment of copy number variation in Age-related Macular Degeneration. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38343


Washington University in St. Louis

26. Schlosberg, Christopher E. Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change.

Degree: PhD, Biology & Biomedical Sciences (Computational & Systems Biology), 2017, Washington University in St. Louis

 Gene expression is driven by specific combinations of transcription factors binding to regulatory sequences to define cell type expression profiles. Changes in DNA sequence alter… (more)

Subjects/Keywords: 5-hydroxymethylcytosine, Cancer Biology, Copy Number Variation, Development, DNA Methylation, Gene Expression; Bioinformatics

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APA (6th Edition):

Schlosberg, C. E. (2017). Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/1143

Chicago Manual of Style (16th Edition):

Schlosberg, Christopher E. “Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change.” 2017. Doctoral Dissertation, Washington University in St. Louis. Accessed October 31, 2020. https://openscholarship.wustl.edu/art_sci_etds/1143.

MLA Handbook (7th Edition):

Schlosberg, Christopher E. “Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change.” 2017. Web. 31 Oct 2020.

Vancouver:

Schlosberg CE. Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2017. [cited 2020 Oct 31]. Available from: https://openscholarship.wustl.edu/art_sci_etds/1143.

Council of Science Editors:

Schlosberg CE. Modeling Complex Patterns of Differential DNA Methylation That Associate with Expression Change. [Doctoral Dissertation]. Washington University in St. Louis; 2017. Available from: https://openscholarship.wustl.edu/art_sci_etds/1143


University of Melbourne

27. Ganesamoorthy, Devika. Cell-free DNA chimerism analysis and clinical applications.

Degree: 2013, University of Melbourne

 Cell-free DNA chimerism describes the co-existence of cell-free DNA originating from more than one individual. The most obvious examples are donor-recipient DNA mixtures in the… (more)

Subjects/Keywords: cell-free DNA; massively parallel sequencing; copy number variation; renal transplant; non-invasive prenatal diagnosis

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APA (6th Edition):

Ganesamoorthy, D. (2013). Cell-free DNA chimerism analysis and clinical applications. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38584

Chicago Manual of Style (16th Edition):

Ganesamoorthy, Devika. “Cell-free DNA chimerism analysis and clinical applications.” 2013. Doctoral Dissertation, University of Melbourne. Accessed October 31, 2020. http://hdl.handle.net/11343/38584.

MLA Handbook (7th Edition):

Ganesamoorthy, Devika. “Cell-free DNA chimerism analysis and clinical applications.” 2013. Web. 31 Oct 2020.

Vancouver:

Ganesamoorthy D. Cell-free DNA chimerism analysis and clinical applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11343/38584.

Council of Science Editors:

Ganesamoorthy D. Cell-free DNA chimerism analysis and clinical applications. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38584


University of Southern California

28. Warden, Melissa Brooke. Genomic risk factors associated with Ewing Sarcoma susceptibility.

Degree: PhD, Molecular Epidemiology, 2012, University of Southern California

 Ewing Sarcoma (EWS) is malignant tumor of bone or soft tissue that primarily affects children and adolescents. Most EWS tumors share the oncogenic fusion protein… (more)

Subjects/Keywords: single nucleotide polymorphism; copy number variation; genome-wide association study; Ewing Sarcoma

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APA (6th Edition):

Warden, M. B. (2012). Genomic risk factors associated with Ewing Sarcoma susceptibility. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/28196/rec/3022

Chicago Manual of Style (16th Edition):

Warden, Melissa Brooke. “Genomic risk factors associated with Ewing Sarcoma susceptibility.” 2012. Doctoral Dissertation, University of Southern California. Accessed October 31, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/28196/rec/3022.

MLA Handbook (7th Edition):

Warden, Melissa Brooke. “Genomic risk factors associated with Ewing Sarcoma susceptibility.” 2012. Web. 31 Oct 2020.

Vancouver:

Warden MB. Genomic risk factors associated with Ewing Sarcoma susceptibility. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Oct 31]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/28196/rec/3022.

Council of Science Editors:

Warden MB. Genomic risk factors associated with Ewing Sarcoma susceptibility. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/28196/rec/3022


The Ohio State University

29. Rutherford, Andrea Marie. Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients.

Degree: MS, Molecular, Cellular and Developmental Biology, 2012, The Ohio State University

  Proper metabolism of food, especially glucose, is vital to an organism’s survival. Failure to metabolize polysaccharides and regulate blood glucose levels are hallmarks of… (more)

Subjects/Keywords: Genetics; copy number variation; amylase; type 1 diabetes; genetics; pulsed field gel electrophoresis; segmental duplication

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APA (6th Edition):

Rutherford, A. M. (2012). Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1337716744

Chicago Manual of Style (16th Edition):

Rutherford, Andrea Marie. “Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients.” 2012. Masters Thesis, The Ohio State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1337716744.

MLA Handbook (7th Edition):

Rutherford, Andrea Marie. “Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients.” 2012. Web. 31 Oct 2020.

Vancouver:

Rutherford AM. Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients. [Internet] [Masters thesis]. The Ohio State University; 2012. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337716744.

Council of Science Editors:

Rutherford AM. Elucidation of Pattern of Variation for the Amylase Locus in Type 1 Diabetes Patients. [Masters Thesis]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337716744

30. Silmara Cristiane da Silveira. Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos.

Degree: 2013, Universidade Católica de Brasilia

Com os avanços recentes da análise genômica, foi possível identificar extensivas variações estruturais em fragmentos gênicos que variam de kilobases (kb) a megabases (Mb), que… (more)

Subjects/Keywords: cólon (anatomia); câncer; genes; fisiopatologia; biotecnologia; GENETICA; colorectal cancer; MicroRNA; copy number variation (CNV); GENETICA

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

APA (6th Edition):

Silveira, S. C. d. (2013). Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos. (Masters Thesis). Universidade Católica de Brasilia. Retrieved from http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=1836

Chicago Manual of Style (16th Edition):

Silveira, Silmara Cristiane da. “Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos.” 2013. Masters Thesis, Universidade Católica de Brasilia. Accessed October 31, 2020. http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=1836.

MLA Handbook (7th Edition):

Silveira, Silmara Cristiane da. “Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos.” 2013. Web. 31 Oct 2020.

Vancouver:

Silveira SCd. Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos. [Internet] [Masters thesis]. Universidade Católica de Brasilia; 2013. [cited 2020 Oct 31]. Available from: http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=1836.

Council of Science Editors:

Silveira SCd. Análise de "Copy Number Variation" contendo genes de microRNA em indivíduos com câncer colorretal e associação com desfechos clínicos. [Masters Thesis]. Universidade Católica de Brasilia; 2013. Available from: http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=1836

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