Advanced search options

Advanced Search Options 🞨

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

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Copy number). Showing records 1 – 30 of 361 total matches.

[1] [2] [3] [4] [5] … [13]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Utah

1. Sankaranarayanan, Preethi. Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival.

Degree: MS, Bioengineering, 2013, University of Utah

 Despite recent large-scale profiling efforts, the best prognostic predictor ofglioblastoma multiforme (GBM) remains the patient’s age at diagnosis. Wedescribe a global pattern of tumor-exclusive co-occurring… (more)

Subjects/Keywords: Copy number; Glioblastoma multiforme; GSVD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sankaranarayanan, P. (2013). Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2111/rec/1101

Chicago Manual of Style (16th Edition):

Sankaranarayanan, Preethi. “Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival.” 2013. Masters Thesis, University of Utah. Accessed December 04, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2111/rec/1101.

MLA Handbook (7th Edition):

Sankaranarayanan, Preethi. “Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival.” 2013. Web. 04 Dec 2020.

Vancouver:

Sankaranarayanan P. Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival. [Internet] [Masters thesis]. University of Utah; 2013. [cited 2020 Dec 04]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2111/rec/1101.

Council of Science Editors:

Sankaranarayanan P. Generalized singular value decomposition (GSVD) comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survival. [Masters Thesis]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2111/rec/1101

2. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 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 December 04, 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. 04 Dec 2020.

Vancouver:

Huang N. The functional impact of copy number variation in the human genome. [Internet] [Doctoral dissertation]. University of Cambridge; 2012. [cited 2020 Dec 04]. 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


University of Edinburgh

3. Chen, Wanting. Copy Number Variants in the human genome and their association with quantitative traits.

Degree: PhD, 2011, University of Edinburgh

Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence, are a main form of genetic variation between individual genomes. CNVs are… (more)

Subjects/Keywords: 576.58; Copy number Variants; CNV

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, W. (2011). Copy Number Variants in the human genome and their association with quantitative traits. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5957

Chicago Manual of Style (16th Edition):

Chen, Wanting. “Copy Number Variants in the human genome and their association with quantitative traits.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed December 04, 2020. http://hdl.handle.net/1842/5957.

MLA Handbook (7th Edition):

Chen, Wanting. “Copy Number Variants in the human genome and their association with quantitative traits.” 2011. Web. 04 Dec 2020.

Vancouver:

Chen W. Copy Number Variants in the human genome and their association with quantitative traits. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1842/5957.

Council of Science Editors:

Chen W. Copy Number Variants in the human genome and their association with quantitative traits. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5957


Colorado State University

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 2020. http://hdl.handle.net/10217/191411.

MLA Handbook (7th Edition):

Sedam, Hailey Nicole Conover. “Genome instability: a pre-existing condition.” 2018. Web. 04 Dec 2020.

Vancouver:

Sedam HNC. Genome instability: a pre-existing condition. [Internet] [Doctoral dissertation]. Colorado State University; 2018. [cited 2020 Dec 04]. 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

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 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. 04 Dec 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 Dec 04]. 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 Toronto

6. Samuel, Nardin. Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target.

Degree: 2012, University of Toronto

This study presents an integrated analysis of pancreatic ductal adenocarcinomas (PDACs) for identification of putative cancer driver genes in somatic copy number gains (SCNGs). SCNG… (more)

Subjects/Keywords: Pancreatic Cancer; Copy Number Gains; 0369; 0992

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Samuel, N. (2012). Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33516

Chicago Manual of Style (16th Edition):

Samuel, Nardin. “Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target.” 2012. Masters Thesis, University of Toronto. Accessed December 04, 2020. http://hdl.handle.net/1807/33516.

MLA Handbook (7th Edition):

Samuel, Nardin. “Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target.” 2012. Web. 04 Dec 2020.

Vancouver:

Samuel N. Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1807/33516.

Council of Science Editors:

Samuel N. Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33516


University of Adelaide

7. McMichael, Gai Lisette. The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?.

Degree: 2012, University of Adelaide

 Background Cerebral palsy describes a group of permanent disorders of the development of movement and posture that are attributed to non-progressive disturbances occurring in the… (more)

Subjects/Keywords: Cerebral palsy; copy number variants; genetics; inheritance

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

McMichael, G. L. (2012). The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/103578

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):

McMichael, Gai Lisette. “The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?.” 2012. Thesis, University of Adelaide. Accessed December 04, 2020. http://hdl.handle.net/2440/103578.

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

MLA Handbook (7th Edition):

McMichael, Gai Lisette. “The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?.” 2012. Web. 04 Dec 2020.

Vancouver:

McMichael GL. The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2440/103578.

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

Council of Science Editors:

McMichael GL. The genomics of cerebral palsy : are copy number variants associated with cerebral palsy?. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/103578

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

8. Michel, Agnès. Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing.

Degree: 2005, Université de Genève

 Chez la levure "S.cerevisiae", l'ADN ribosomal (ADNr) est constitué par environ 200 répétitions en tandem des séquences codant pour les ARN ribosomaux et dont le… (more)

Subjects/Keywords: rDNA copy number

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Michel, A. (2005). Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing. (Thesis). Université de Genève. Retrieved from http://doc.rero.ch/record/8062

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):

Michel, Agnès. “Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing.” 2005. Thesis, Université de Genève. Accessed December 04, 2020. http://doc.rero.ch/record/8062.

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

MLA Handbook (7th Edition):

Michel, Agnès. “Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing.” 2005. Web. 04 Dec 2020.

Vancouver:

Michel A. Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing. [Internet] [Thesis]. Université de Genève; 2005. [cited 2020 Dec 04]. Available from: http://doc.rero.ch/record/8062.

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

Council of Science Editors:

Michel A. Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing. [Thesis]. Université de Genève; 2005. Available from: http://doc.rero.ch/record/8062

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


University of Iowa

9. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 2020. https://ir.uiowa.edu/etd/4739.

MLA Handbook (7th Edition):

Rudd, Danielle Song. “Genomic copy number variation in schizophrenia.” 2014. Web. 04 Dec 2020.

Vancouver:

Rudd DS. Genomic copy number variation in schizophrenia. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2020 Dec 04]. 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

10. Dentro, Stefan Christiaan. The Intra-Tumour Heterogeneity Landscape of Human Cancers.

Degree: PhD, 2020, University of Cambridge

 Tumours accumulate many somatic mutations in their lifetime. Some of these mutations, drivers, convey a selective advantage and can induce clonal expansions. Incomplete clonal expansions… (more)

Subjects/Keywords: Cancer; Sequencing; Copy Number Alterations; Subclonal Architecture

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dentro, S. C. (2020). The Intra-Tumour Heterogeneity Landscape of Human Cancers. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/301149

Chicago Manual of Style (16th Edition):

Dentro, Stefan Christiaan. “The Intra-Tumour Heterogeneity Landscape of Human Cancers.” 2020. Doctoral Dissertation, University of Cambridge. Accessed December 04, 2020. https://www.repository.cam.ac.uk/handle/1810/301149.

MLA Handbook (7th Edition):

Dentro, Stefan Christiaan. “The Intra-Tumour Heterogeneity Landscape of Human Cancers.” 2020. Web. 04 Dec 2020.

Vancouver:

Dentro SC. The Intra-Tumour Heterogeneity Landscape of Human Cancers. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Dec 04]. Available from: https://www.repository.cam.ac.uk/handle/1810/301149.

Council of Science Editors:

Dentro SC. The Intra-Tumour Heterogeneity Landscape of Human Cancers. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/301149


University of Cambridge

11. Gregson, Eleanor. Characterisation of copy number changes in the progression of Barrett's oesophagus.

Degree: PhD, 2018, University of Cambridge

 Introduction: The main risk factor for the development of oesophageal adenocarcinoma is Barrett’s oesophagus (BE). To diagnose those patients who will progress to cancer early… (more)

Subjects/Keywords: 616.3; Barrett's Oesophagus; Oesophageal adenocarcinoma; Copy number

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gregson, E. (2018). Characterisation of copy number changes in the progression of Barrett's oesophagus. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.26000 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753403

Chicago Manual of Style (16th Edition):

Gregson, Eleanor. “Characterisation of copy number changes in the progression of Barrett's oesophagus.” 2018. Doctoral Dissertation, University of Cambridge. Accessed December 04, 2020. https://doi.org/10.17863/CAM.26000 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753403.

MLA Handbook (7th Edition):

Gregson, Eleanor. “Characterisation of copy number changes in the progression of Barrett's oesophagus.” 2018. Web. 04 Dec 2020.

Vancouver:

Gregson E. Characterisation of copy number changes in the progression of Barrett's oesophagus. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Dec 04]. Available from: https://doi.org/10.17863/CAM.26000 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753403.

Council of Science Editors:

Gregson E. Characterisation of copy number changes in the progression of Barrett's oesophagus. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.26000 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753403


University of Cambridge

12. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 December 04, 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. 04 Dec 2020.

Vancouver:

Huang N. The functional impact of copy number variation in the human genome. [Internet] [Doctoral dissertation]. University of Cambridge; 2012. [cited 2020 Dec 04]. 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 Cambridge

13. Dentro, Stefan Christiaan. The intra-tumour heterogeneity landscape of human cancers.

Degree: PhD, 2020, University of Cambridge

 Tumours accumulate many somatic mutations in their lifetime. Some of these mutations, drivers, convey a selective advantage and can induce clonal expansions. Incomplete clonal expansions… (more)

Subjects/Keywords: Cancer; Sequencing; Copy Number Alterations; Subclonal Architecture

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dentro, S. C. (2020). The intra-tumour heterogeneity landscape of human cancers. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.48225 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801675

Chicago Manual of Style (16th Edition):

Dentro, Stefan Christiaan. “The intra-tumour heterogeneity landscape of human cancers.” 2020. Doctoral Dissertation, University of Cambridge. Accessed December 04, 2020. https://doi.org/10.17863/CAM.48225 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801675.

MLA Handbook (7th Edition):

Dentro, Stefan Christiaan. “The intra-tumour heterogeneity landscape of human cancers.” 2020. Web. 04 Dec 2020.

Vancouver:

Dentro SC. The intra-tumour heterogeneity landscape of human cancers. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Dec 04]. Available from: https://doi.org/10.17863/CAM.48225 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801675.

Council of Science Editors:

Dentro SC. The intra-tumour heterogeneity landscape of human cancers. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.48225 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801675


University of Notre Dame

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 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. 04 Dec 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 Dec 04]. 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


Virginia Tech

15. Hou, Xuchu. Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications.

Degree: MS, Computer Engineering, 2013, Virginia Tech

 Somatic Copy Number Alterations (CNAs) are common events in human cancers. Identifying CNAs and Significant Copy number Aberrations (SCAs) in cancer genomes is a critical… (more)

Subjects/Keywords: Copy Number Alterations; Normal Tissue Contamination; Significant Copy number Aberrations; Concurrent Computing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hou, X. (2013). Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/19235

Chicago Manual of Style (16th Edition):

Hou, Xuchu. “Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications.” 2013. Masters Thesis, Virginia Tech. Accessed December 04, 2020. http://hdl.handle.net/10919/19235.

MLA Handbook (7th Edition):

Hou, Xuchu. “Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications.” 2013. Web. 04 Dec 2020.

Vancouver:

Hou X. Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications. [Internet] [Masters thesis]. Virginia Tech; 2013. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10919/19235.

Council of Science Editors:

Hou X. Accurate Identification of Significant Aberrations in Cancer Genome: Implementation and Applications. [Masters Thesis]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/19235


NSYSU

16. Yeh, Yi-Hsing. Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma.

Degree: Master, Biological Sciences, 2015, NSYSU

 Intrahepatic cholangiocarcinoma (ICC) is relatively infrequent, accounting for 5-15% of primary liver cancer worldwide. The risk factors include chronic inflammatory biliary disease, hepatolithiasis, parasitic biliary… (more)

Subjects/Keywords: KIF14; TPM3; ADAMTSL4; copy number alterations; Intrahepatic cholangiocarcinoma

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yeh, Y. (2015). Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816115-174947

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):

Yeh, Yi-Hsing. “Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma.” 2015. Thesis, NSYSU. Accessed December 04, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816115-174947.

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

MLA Handbook (7th Edition):

Yeh, Yi-Hsing. “Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma.” 2015. Web. 04 Dec 2020.

Vancouver:

Yeh Y. Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma. [Internet] [Thesis]. NSYSU; 2015. [cited 2020 Dec 04]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816115-174947.

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

Council of Science Editors:

Yeh Y. Copy number alterations of chromosome 1q in intrahepatic cholangiocarcinoma. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816115-174947

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


University of Alberta

17. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 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. 04 Dec 2020.

Vancouver:

Khorshidi A. Study of the molecular cause of anophthalmia in a consanguineous pedigree. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Dec 04]. 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 Michigan

18. Park, So Hae. Role of Transcription in Mammalian Copy Number Variant Formation.

Degree: PhD, Human Genetics, 2018, University of Michigan

 Genome instability, defined as an increased tendency of genome alteration, is the cause of many human diseases and conditions. It is a hallmark of human… (more)

Subjects/Keywords: Copy number variants; Transcription; Genome instability; R-loops; Genetics; Science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Park, S. H. (2018). Role of Transcription in Mammalian Copy Number Variant Formation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/147729

Chicago Manual of Style (16th Edition):

Park, So Hae. “Role of Transcription in Mammalian Copy Number Variant Formation.” 2018. Doctoral Dissertation, University of Michigan. Accessed December 04, 2020. http://hdl.handle.net/2027.42/147729.

MLA Handbook (7th Edition):

Park, So Hae. “Role of Transcription in Mammalian Copy Number Variant Formation.” 2018. Web. 04 Dec 2020.

Vancouver:

Park SH. Role of Transcription in Mammalian Copy Number Variant Formation. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2027.42/147729.

Council of Science Editors:

Park SH. Role of Transcription in Mammalian Copy Number Variant Formation. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/147729


Texas A&M University

19. Hsu, Fang-Han. Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application.

Degree: PhD, Electrical Engineering, 2013, Texas A&M University

 The advances of high-throughput technologies, such as next-generation sequencing and microarrays, have rapidly improved the accessibility of molecular profiles in tumor samples. However, due to… (more)

Subjects/Keywords: copy number alterations; gene expression; queueing theory; Bayesian network; drug effectiveness

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hsu, F. (2013). Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149298

Chicago Manual of Style (16th Edition):

Hsu, Fang-Han. “Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application.” 2013. Doctoral Dissertation, Texas A&M University. Accessed December 04, 2020. http://hdl.handle.net/1969.1/149298.

MLA Handbook (7th Edition):

Hsu, Fang-Han. “Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application.” 2013. Web. 04 Dec 2020.

Vancouver:

Hsu F. Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1969.1/149298.

Council of Science Editors:

Hsu F. Copy Number and Gene Expression: Stochastic Modeling and Therapeutic Application. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149298


Texas A&M University

20. Doan, Ryan. The Identification and Characterization of Copy Number Variants in the Bovine Genome.

Degree: PhD, Genetics, 2013, Texas A&M University

 Separate domestication events and strong selective pressures have created diverse phenotypes among existing cattle populations; however, the genetic determinants underlying most phenotypes are currently unknown.… (more)

Subjects/Keywords: Genetic variants; epigenetics; regulatory elements; cattle; copy number variants

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Doan, R. (2013). The Identification and Characterization of Copy Number Variants in the Bovine Genome. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151022

Chicago Manual of Style (16th Edition):

Doan, Ryan. “The Identification and Characterization of Copy Number Variants in the Bovine Genome.” 2013. Doctoral Dissertation, Texas A&M University. Accessed December 04, 2020. http://hdl.handle.net/1969.1/151022.

MLA Handbook (7th Edition):

Doan, Ryan. “The Identification and Characterization of Copy Number Variants in the Bovine Genome.” 2013. Web. 04 Dec 2020.

Vancouver:

Doan R. The Identification and Characterization of Copy Number Variants in the Bovine Genome. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1969.1/151022.

Council of Science Editors:

Doan R. The Identification and Characterization of Copy Number Variants in the Bovine Genome. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151022


McMaster University

21. Ghenu, Ana-Hermina. Multicopy gene family evolution on primate Y chromosomes.

Degree: MSc, 2015, McMaster University

Unlike the autosomes, the Y chromosome in humans and other primates has few protein coding genes, with only a few dozen single-copy genes and several… (more)

Subjects/Keywords: Y chromosome; gene copy number evolution; Old World Primates; genome structure

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ghenu, A. (2015). Multicopy gene family evolution on primate Y chromosomes. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/18277

Chicago Manual of Style (16th Edition):

Ghenu, Ana-Hermina. “Multicopy gene family evolution on primate Y chromosomes.” 2015. Masters Thesis, McMaster University. Accessed December 04, 2020. http://hdl.handle.net/11375/18277.

MLA Handbook (7th Edition):

Ghenu, Ana-Hermina. “Multicopy gene family evolution on primate Y chromosomes.” 2015. Web. 04 Dec 2020.

Vancouver:

Ghenu A. Multicopy gene family evolution on primate Y chromosomes. [Internet] [Masters thesis]. McMaster University; 2015. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/11375/18277.

Council of Science Editors:

Ghenu A. Multicopy gene family evolution on primate Y chromosomes. [Masters Thesis]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18277


Penn State University

22. Vegesna, Rahulsimham. Evolution of Y chromosome ampliconic genes in great apes.

Degree: 2020, Penn State University

 In addition to the sex-determining gene SRY and several other single-copy genes, the human Y chromosome harbors nine multi-copy gene families which are expressed exclusively… (more)

Subjects/Keywords: Y chromosome; Great apes; Ampliconic genes; Palindromes; Copy number; Evolution

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vegesna, R. (2020). Evolution of Y chromosome ampliconic genes in great apes. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17460rxv923

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):

Vegesna, Rahulsimham. “Evolution of Y chromosome ampliconic genes in great apes.” 2020. Thesis, Penn State University. Accessed December 04, 2020. https://submit-etda.libraries.psu.edu/catalog/17460rxv923.

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

MLA Handbook (7th Edition):

Vegesna, Rahulsimham. “Evolution of Y chromosome ampliconic genes in great apes.” 2020. Web. 04 Dec 2020.

Vancouver:

Vegesna R. Evolution of Y chromosome ampliconic genes in great apes. [Internet] [Thesis]. Penn State University; 2020. [cited 2020 Dec 04]. Available from: https://submit-etda.libraries.psu.edu/catalog/17460rxv923.

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

Council of Science Editors:

Vegesna R. Evolution of Y chromosome ampliconic genes in great apes. [Thesis]. Penn State University; 2020. Available from: https://submit-etda.libraries.psu.edu/catalog/17460rxv923

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


Queens University

23. Williams, Julia. Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions .

Degree: Pathology and Molecular Medicine, 2014, Queens University

 Prostate cancer is a clinically heterogeneous disease, with manifestations ranging from a rapid and often fatal progression, to indolent disease. Unfortunately, current clinicopathological criteria cannot… (more)

Subjects/Keywords: Copy Number ; PTEN ; Genomic ; TMPRSS2:ERG ; ETS Gene Fusions ; Prostate Cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, J. (2014). Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12146

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):

Williams, Julia. “Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions .” 2014. Thesis, Queens University. Accessed December 04, 2020. http://hdl.handle.net/1974/12146.

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

MLA Handbook (7th Edition):

Williams, Julia. “Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions .” 2014. Web. 04 Dec 2020.

Vancouver:

Williams J. Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions . [Internet] [Thesis]. Queens University; 2014. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1974/12146.

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

Council of Science Editors:

Williams J. Recurrent Copy Number Alterations in Prostate Cancer: the Genomic Impact of PTEN Deletions and the Prostate-Specific ETS Gene Fusions . [Thesis]. Queens University; 2014. Available from: http://hdl.handle.net/1974/12146

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


University of Toronto

24. Trick, Sudhir Jonathan. Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis.

Degree: 2014, University of Toronto

Li-Fraumeni syndrome (LFS) is a highly penetrant familial cancer syndrome associated with inherited germline mutations in TP53. However, a causative gene has not been identified… (more)

Subjects/Keywords: Cancer Syndromes; Copy Number Variants; Genetics; Genomics; Microarray; Oncology; 0369

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Trick, S. J. (2014). Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68013

Chicago Manual of Style (16th Edition):

Trick, Sudhir Jonathan. “Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis.” 2014. Masters Thesis, University of Toronto. Accessed December 04, 2020. http://hdl.handle.net/1807/68013.

MLA Handbook (7th Edition):

Trick, Sudhir Jonathan. “Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis.” 2014. Web. 04 Dec 2020.

Vancouver:

Trick SJ. Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1807/68013.

Council of Science Editors:

Trick SJ. Identification of Cancer Susceptibility Loci by High-resolution Cancer Gene Microarray Analysis. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68013


Harvard University

25. Zack, Travis Ian. Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations.

Degree: PhD, Biophysics, 2014, Harvard University

 Somatic copy number alterations (SCNAs) are a class of alterations that lead to deviations from diploidy in developing and established tumors. A feature that distinguishes… (more)

Subjects/Keywords: Bioinformatics; Cellular biology; Biostatistics; Cancer; cancer dependency; Copy number; non-driver

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zack, T. I. (2014). Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13065031

Chicago Manual of Style (16th Edition):

Zack, Travis Ian. “Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations.” 2014. Doctoral Dissertation, Harvard University. Accessed December 04, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13065031.

MLA Handbook (7th Edition):

Zack, Travis Ian. “Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations.” 2014. Web. 04 Dec 2020.

Vancouver:

Zack TI. Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Dec 04]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13065031.

Council of Science Editors:

Zack TI. Exploring Cancer's Fractured Genomic Landscape: Searching for Cancer Drivers and Vulnerabilities in Somatic Copy Number Alterations. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13065031


Universidade Nova

26. Saramago, Ana Alexandra Figueiredo Gonçalves. Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X.

Degree: 2015, Universidade Nova

 O cancro do cólon e reto familiar do tipo X (FCCTX) é um síndrome que define as famílias que preenchem os critérios de Amesterdão, mas… (more)

Subjects/Keywords: FCCTX; Mutações germinais; Genes de suscetibilidade; Metilação; Copy-number

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Saramago, A. A. F. G. (2015). Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14192

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):

Saramago, Ana Alexandra Figueiredo Gonçalves. “Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X.” 2015. Thesis, Universidade Nova. Accessed December 04, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14192.

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

MLA Handbook (7th Edition):

Saramago, Ana Alexandra Figueiredo Gonçalves. “Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X.” 2015. Web. 04 Dec 2020.

Vancouver:

Saramago AAFG. Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X. [Internet] [Thesis]. Universidade Nova; 2015. [cited 2020 Dec 04]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14192.

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

Council of Science Editors:

Saramago AAFG. Estudo de mutações germinais em genes de suscetibilidade para o cancro do colón e reto familiar do tipo X. [Thesis]. Universidade Nova; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/14192

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


University of Guelph

27. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 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. 04 Dec 2020.

Vancouver:

Quach A. INVESTIGATION OF GENOME VARIATIONS AS POTENTIAL MARKERS FOR BOAR FERTILITY. [Internet] [Doctoral dissertation]. University of Guelph; 2015. [cited 2020 Dec 04]. 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 Guelph

28. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 December 04, 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. 04 Dec 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 Dec 04]. 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

29. 조, 효정. Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up.

Degree: 2016, Ajou University

Aims The aim of this study was to explore for novel genomic biomarker predicting hepatocellular carcinoma (HCC) prognosis by integrative analysis of DNA copy number(more)

Subjects/Keywords: hepatocellular carcinoma; integrative analysis; copy number aberration; expression; prognosis; biomarker

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

조, . (2016). Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/13047 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021435

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):

조, 효정. “Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up.” 2016. Thesis, Ajou University. Accessed December 04, 2020. http://repository.ajou.ac.kr/handle/201003/13047 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021435.

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

MLA Handbook (7th Edition):

조, 효정. “Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up.” 2016. Web. 04 Dec 2020.

Vancouver:

조 . Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up. [Internet] [Thesis]. Ajou University; 2016. [cited 2020 Dec 04]. Available from: http://repository.ajou.ac.kr/handle/201003/13047 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021435.

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

Council of Science Editors:

조 . Detection of Novel Genomic Markers for Predicting Prognosis in Hepatocellular Carcinoma Patients by Integrative Analysis of Copy Number Aberrations and Gene Expression Profiles: Results from a Long-Term Follow-Up. [Thesis]. Ajou University; 2016. Available from: http://repository.ajou.ac.kr/handle/201003/13047 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021435

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


University of Cambridge

30. Al-Khalidi, Sarwah. Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma.

Degree: PhD, 2020, University of Cambridge

 Despite increasing reports indicating the prognostic significance of immune cell abundance in high grade serous ovarian cancer (HGSOC), mutational processes by which tumours gain immunogenicity… (more)

Subjects/Keywords: Cancer; Ovarian; immune; Immun-Oncology; Oncology; Genomic Aberration; Copy number alterations

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Al-Khalidi, S. (2020). Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303391

Chicago Manual of Style (16th Edition):

Al-Khalidi, Sarwah. “Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma.” 2020. Doctoral Dissertation, University of Cambridge. Accessed December 04, 2020. https://www.repository.cam.ac.uk/handle/1810/303391.

MLA Handbook (7th Edition):

Al-Khalidi, Sarwah. “Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma.” 2020. Web. 04 Dec 2020.

Vancouver:

Al-Khalidi S. Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Dec 04]. Available from: https://www.repository.cam.ac.uk/handle/1810/303391.

Council of Science Editors:

Al-Khalidi S. Genomic aberrations as determinants of immune infiltrates in high grade serous ovarian carcinoma. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303391

[1] [2] [3] [4] [5] … [13]

.