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You searched for subject:(Copy number variations CNVs ). Showing records 1 – 30 of 4981 total matches.

[1] [2] [3] [4] [5] … [167]

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University of Toronto

1. Gazzellone, Joseph Matthew. Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder.

Degree: 2014, University of Toronto

Autism spectrum disorders (ASDs) are a group of neurodevelopmental conditions with a demonstrated genetic etiology. Rare copy number variations (CNVs) account for a proportion of… (more)

Subjects/Keywords: Autism spectrum disorder (ASD); Copy number variations (CNVs); Han Chinese; Microarray diagnostic testing; 0369

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

APA (6th Edition):

Gazzellone, J. M. (2014). Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68053

Chicago Manual of Style (16th Edition):

Gazzellone, Joseph Matthew. “Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder.” 2014. Masters Thesis, University of Toronto. Accessed October 28, 2020. http://hdl.handle.net/1807/68053.

MLA Handbook (7th Edition):

Gazzellone, Joseph Matthew. “Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder.” 2014. Web. 28 Oct 2020.

Vancouver:

Gazzellone JM. Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1807/68053.

Council of Science Editors:

Gazzellone JM. Copy Number Variation in Han Chinese Individuals with Autism Spectrum Disorder. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68053

2. S. Sinha. Detection of structural variations during liver cancer progression.

Degree: 2015, Università degli Studi di Milano

 Hepatocellular carcinoma (HCC) is one of the most lethal cancers in the world and accounts for the vast majority of all liver cancers. HCC develops… (more)

Subjects/Keywords: Hepatocelluar carcinoma; BSEP-HCC; copy number variations; GeneCNV; CNVs; JNK; Settore MED/04 - Patologia Generale

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APA (6th Edition):

Sinha, S. (2015). Detection of structural variations during liver cancer progression. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/265927

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):

Sinha, S.. “Detection of structural variations during liver cancer progression.” 2015. Thesis, Università degli Studi di Milano. Accessed October 28, 2020. http://hdl.handle.net/2434/265927.

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

MLA Handbook (7th Edition):

Sinha, S.. “Detection of structural variations during liver cancer progression.” 2015. Web. 28 Oct 2020.

Vancouver:

Sinha S. Detection of structural variations during liver cancer progression. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2434/265927.

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

Council of Science Editors:

Sinha S. Detection of structural variations during liver cancer progression. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/265927

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

3. Giannikou, Krinio. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Intellectual Disability (ID) is a very clinically and genetically heterogeneous neurodevelopmental entity, thus raising difficulties on genetic evaluation and diagnosis. Hitherto, only a few cases… (more)

Subjects/Keywords: Μικροσυστοιχίες συγκριτικού γενωμικού υβριδισμού; Νοητική υστέρηση; Ποικιλομορφίες αριθμού αντιγράφων; Μικροελλείμματα/Μικροδιπλασιασμοί; Μοριακός καρυότυπος; Microarray comparative genomic hybridization; Intellectual disability; Copy number variations (CNVs); Microdeletion/Microduplication; Molecular karyotyping

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APA (6th Edition):

Giannikou, K. (2014). Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42161

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):

Giannikou, Krinio. “Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 28, 2020. http://hdl.handle.net/10442/hedi/42161.

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

MLA Handbook (7th Edition):

Giannikou, Krinio. “Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).” 2014. Web. 28 Oct 2020.

Vancouver:

Giannikou K. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10442/hedi/42161.

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

Council of Science Editors:

Giannikou K. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/42161

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

4. 이, 형남. Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.

Degree: 2017, Ajou University

BACKGROUND: Chromosomal microarray (CMA) is a cytogenetic diagnostic test for chromosomal abnormalities in many diseases, which can provide the fast and accurate detection of copy-number(more)

Subjects/Keywords: Chromosomal microarray (CMA); Copy-number variations (CNVs); Congenital anomaly; Developmental delay (DD); Intellectual disability (ID); 염색체 마이크로어레이; 복제수변이; 신경발달장애; 선천성 기형; 발달지연; 지적장애

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APA (6th Edition):

이, . (2017). Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829

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):

이, 형남. “Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.” 2017. Thesis, Ajou University. Accessed October 28, 2020. http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829.

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

MLA Handbook (7th Edition):

이, 형남. “Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.” 2017. Web. 28 Oct 2020.

Vancouver:

이 . Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. [Internet] [Thesis]. Ajou University; 2017. [cited 2020 Oct 28]. Available from: http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829.

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

Council of Science Editors:

이 . Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. [Thesis]. Ajou University; 2017. Available from: http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829

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

5. 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 28, 2020. http://hdl.handle.net/1807/68128.

MLA Handbook (7th Edition):

Lionel, Christopher Anath. “Copy Number Variation in Neurodevelopmental Disorders.” 2014. Web. 28 Oct 2020.

Vancouver:

Lionel CA. Copy Number Variation in Neurodevelopmental Disorders. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Oct 28]. 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 Otago

6. Moir-Meyer, Gemma Louise. Endometrial Cancer and Copy Number Variation .

Degree: 2013, University of Otago

 Endometrial cancer is the most common gynaecological cancer in New Zealand and the incidence is increasing as the population ages. Genetic predictors of endometrial cancer… (more)

Subjects/Keywords: copy number variation; CNV; loading; CNV load; mismatch repair pathway; candidate gene; MSH2; MSH6; MUTYH; RPA3; TGFBR3; genome wide association study; GWAS; PennCNV; CNV frequency; rare CNVs; common CNVs; deletion; duplication; copy number gain; copy number loss; endometrial cancer

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APA (6th Edition):

Moir-Meyer, G. L. (2013). Endometrial Cancer and Copy Number Variation . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/4170

Chicago Manual of Style (16th Edition):

Moir-Meyer, Gemma Louise. “Endometrial Cancer and Copy Number Variation .” 2013. Masters Thesis, University of Otago. Accessed October 28, 2020. http://hdl.handle.net/10523/4170.

MLA Handbook (7th Edition):

Moir-Meyer, Gemma Louise. “Endometrial Cancer and Copy Number Variation .” 2013. Web. 28 Oct 2020.

Vancouver:

Moir-Meyer GL. Endometrial Cancer and Copy Number Variation . [Internet] [Masters thesis]. University of Otago; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10523/4170.

Council of Science Editors:

Moir-Meyer GL. Endometrial Cancer and Copy Number Variation . [Masters Thesis]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4170

7. Mitrakos, Anastasios. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).

Degree: 2020, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Acute Lymphoblastic Leukemia (ALL) is a malignancy of the immature lymphoid cells mainly associated with numerical and structural chromosomal aberrations. The current standard for profiling… (more)

Subjects/Keywords: Συγκριτικός γενωμικός υβριδισμός σε μικροσυστοιχίες; Αιματολογικές κακοήθειες; Αλλαγές αριθμού αντιγράφων (CNVs); Χρωμοσωμική ανάλυση με μικροσυστοιχίες; Array comparative genomic hybridization (aCGH); Hematological malignancies; Copy number variants (CNVs); Chromosomal microarray analysis (CMA)

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APA (6th Edition):

Mitrakos, A. (2020). Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/47723

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):

Mitrakos, Anastasios. “Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).” 2020. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 28, 2020. http://hdl.handle.net/10442/hedi/47723.

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

MLA Handbook (7th Edition):

Mitrakos, Anastasios. “Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).” 2020. Web. 28 Oct 2020.

Vancouver:

Mitrakos A. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10442/hedi/47723.

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

Council of Science Editors:

Mitrakos A. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. Available from: http://hdl.handle.net/10442/hedi/47723

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


Georgia Tech

8. Huang, Tzu-Hsueh. Multidimensional statistics metric in biological data analysis.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Sepsis, a serious body’s response to infection, is still a leading cause of death around the world. Appropriate treatment, however, can take more than three… (more)

Subjects/Keywords: Statistics; Antibiotic susceptibility; Antibiotic resistance; Bacteria; Sepsis; Flow cytometry; Next-generation sequencing; Genome; Copy number variation; CNVs

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APA (6th Edition):

Huang, T. (2017). Multidimensional statistics metric in biological data analysis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60172

Chicago Manual of Style (16th Edition):

Huang, Tzu-Hsueh. “Multidimensional statistics metric in biological data analysis.” 2017. Doctoral Dissertation, Georgia Tech. Accessed October 28, 2020. http://hdl.handle.net/1853/60172.

MLA Handbook (7th Edition):

Huang, Tzu-Hsueh. “Multidimensional statistics metric in biological data analysis.” 2017. Web. 28 Oct 2020.

Vancouver:

Huang T. Multidimensional statistics metric in biological data analysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1853/60172.

Council of Science Editors:

Huang T. Multidimensional statistics metric in biological data analysis. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60172


Harvard University

9. Wang, Jia. Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders.

Degree: Master of Medical Sciences, 2017, Harvard University

Autism Spectrum Disorders have a strong genetic basis. So far, only a small fraction of affected individuals has been linked to a certain genetic risk… (more)

Subjects/Keywords: autism spectrum disorders; copy-number variations; functional enhancers

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APA (6th Edition):

Wang, J. (2017). Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41940983

Chicago Manual of Style (16th Edition):

Wang, Jia. “Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders.” 2017. Masters Thesis, Harvard University. Accessed October 28, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41940983.

MLA Handbook (7th Edition):

Wang, Jia. “Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders.” 2017. Web. 28 Oct 2020.

Vancouver:

Wang J. Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2020 Oct 28]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41940983.

Council of Science Editors:

Wang J. Role of Copy-Number Variations in Non-Coding Regions of Autism Spectrum Disorders. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41940983


University of Toronto

10. Allo, Ghassan. Genomic Characterization of Pleural Solitary Fibrous Tumours.

Degree: 2013, University of Toronto

Pleural solitary fibrous tumours (pSFTs) are uncommon soft tissue tumours of the pleura. that may recur and contribute to the patients’ demise. We analyzed a… (more)

Subjects/Keywords: Solitary fibrous tumours; copy number variations; mutation; paxillin; 0992

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APA (6th Edition):

Allo, G. (2013). Genomic Characterization of Pleural Solitary Fibrous Tumours. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/35578

Chicago Manual of Style (16th Edition):

Allo, Ghassan. “Genomic Characterization of Pleural Solitary Fibrous Tumours.” 2013. Masters Thesis, University of Toronto. Accessed October 28, 2020. http://hdl.handle.net/1807/35578.

MLA Handbook (7th Edition):

Allo, Ghassan. “Genomic Characterization of Pleural Solitary Fibrous Tumours.” 2013. Web. 28 Oct 2020.

Vancouver:

Allo G. Genomic Characterization of Pleural Solitary Fibrous Tumours. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1807/35578.

Council of Science Editors:

Allo G. Genomic Characterization of Pleural Solitary Fibrous Tumours. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35578


George Mason University

11. Espina, Virginia. Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention .

Degree: 2013, George Mason University

 Breast cancer progression is thought to be a multi-step process involving a continuum of changes from a normal phenotype through hyperplastic lesions, carcinoma in situ,… (more)

Subjects/Keywords: ductal carcinoma in situ; autophagy; breast; chemoprevention; chloroquine; copy number variations

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APA (6th Edition):

Espina, V. (2013). Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8299

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):

Espina, Virginia. “Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention .” 2013. Thesis, George Mason University. Accessed October 28, 2020. http://hdl.handle.net/1920/8299.

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

MLA Handbook (7th Edition):

Espina, Virginia. “Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention .” 2013. Web. 28 Oct 2020.

Vancouver:

Espina V. Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention . [Internet] [Thesis]. George Mason University; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1920/8299.

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

Council of Science Editors:

Espina V. Killing Pre-invasive Breast Cancer by Targeting Autophagy: A New Vision for Chemoprevention . [Thesis]. George Mason University; 2013. Available from: http://hdl.handle.net/1920/8299

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

12. Ευαγγελίδου-Μαυρογένη, Πάολα. Μοριακός καρυότυπος στην προγεννητική διάγνωση.

Degree: 2012, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

 Karyotyping has been the golden standard method for prenatal diagnosis fordecades, for the diagnosis of numerical and large structural abnormalities (<3-10Mb).With the introduction of array… (more)

Subjects/Keywords: Προγεννητική διάγνωση; Χρωμοσωμική εξέταση; Συγκριτικός γενομικός υβριδισμός; Ανευπλοειδίες; Πολυμορφισμοί; Prenatal diagnosis; Chromosomal analysis; Microarray comparative genomic hybridization (aCGH); Copy nymber variations (CNVs); Coincidental findings; Pathogenic findings; Aneuploidies; Polymorphisms

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APA (6th Edition):

Ευαγγελίδου-Μαυρογένη, . . (2012). Μοριακός καρυότυπος στην προγεννητική διάγνωση. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/36991

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):

Ευαγγελίδου-Μαυρογένη, Πάολα. “Μοριακός καρυότυπος στην προγεννητική διάγνωση.” 2012. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed October 28, 2020. http://hdl.handle.net/10442/hedi/36991.

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

MLA Handbook (7th Edition):

Ευαγγελίδου-Μαυρογένη, Πάολα. “Μοριακός καρυότυπος στην προγεννητική διάγνωση.” 2012. Web. 28 Oct 2020.

Vancouver:

Ευαγγελίδου-Μαυρογένη . Μοριακός καρυότυπος στην προγεννητική διάγνωση. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2012. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10442/hedi/36991.

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

Council of Science Editors:

Ευαγγελίδου-Μαυρογένη . Μοριακός καρυότυπος στην προγεννητική διάγνωση. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2012. Available from: http://hdl.handle.net/10442/hedi/36991

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


University of Helsinki

13. Saarentaus, Elmo. Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland.

Degree: Medicinska fakulteten, 2017, University of Helsinki

 Genetiska varianter har under senaste åren upptäckts påverka en myriad vanliga samt sällsynta sjukdomar. En viktig grupp varianter i neuropsykiatriska sjukdomar är kromosomavvikelser, speciellt förändringar… (more)

Subjects/Keywords: DNA Copy Number Variations; Intellectual Disability; Genetic Association Studies; Älyllinen kehitysvammaisuus; Geenin deleetio; Geenikopioiden määrä; DNA Copy Number Variations; Intellectual Disability; Genetic Association Studies

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

APA (6th Edition):

Saarentaus, E. (2017). Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/231367

Chicago Manual of Style (16th Edition):

Saarentaus, Elmo. “Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland.” 2017. Masters Thesis, University of Helsinki. Accessed October 28, 2020. http://hdl.handle.net/10138/231367.

MLA Handbook (7th Edition):

Saarentaus, Elmo. “Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland.” 2017. Web. 28 Oct 2020.

Vancouver:

Saarentaus E. Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10138/231367.

Council of Science Editors:

Saarentaus E. Gendosvariationer i neurologiska och utvecklingsrelaterade sjukdomar i Finland. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/231367


University of California – Irvine

14. Tong, Xinhan. Breast Cancer Prediction from Genome Segments with Machine Learning.

Degree: Biomedical Engineering, 2018, University of California – Irvine

 Breast cancer is the most common diagnosed cancer for the worldwide women. Due to the multiformity of the clinical behaviors, it is difficult to predict… (more)

Subjects/Keywords: Biomedical engineering; Computer science; Bioinformatics; Breast Cancer; Copy Number Variations; Machine Learning

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APA (6th Edition):

Tong, X. (2018). Breast Cancer Prediction from Genome Segments with Machine Learning. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/6257h6wf

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):

Tong, Xinhan. “Breast Cancer Prediction from Genome Segments with Machine Learning.” 2018. Thesis, University of California – Irvine. Accessed October 28, 2020. http://www.escholarship.org/uc/item/6257h6wf.

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

MLA Handbook (7th Edition):

Tong, Xinhan. “Breast Cancer Prediction from Genome Segments with Machine Learning.” 2018. Web. 28 Oct 2020.

Vancouver:

Tong X. Breast Cancer Prediction from Genome Segments with Machine Learning. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2020 Oct 28]. Available from: http://www.escholarship.org/uc/item/6257h6wf.

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

Council of Science Editors:

Tong X. Breast Cancer Prediction from Genome Segments with Machine Learning. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/6257h6wf

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


University of Toronto

15. Law, Rosalind. Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene.

Degree: 2014, University of Toronto

Individuals with ID and autism were identified carrying copy number variations within the autosomal recessive intellectual disability gene

M.Sc.

2016-11-18 00:00:00

Advisors/Committee Members: Vincent, John B, Medical Science.

Subjects/Keywords: Autism Spectrum Disorders; Copy Number Variations; Epigenetics; Genomic Imprinting; Intellectual disability; Methylation; 0369

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

APA (6th Edition):

Law, R. (2014). Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74600

Chicago Manual of Style (16th Edition):

Law, Rosalind. “Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene.” 2014. Masters Thesis, University of Toronto. Accessed October 28, 2020. http://hdl.handle.net/1807/74600.

MLA Handbook (7th Edition):

Law, Rosalind. “Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene.” 2014. Web. 28 Oct 2020.

Vancouver:

Law R. Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1807/74600.

Council of Science Editors:

Law R. Analysis of a putative imprinted locus within the TRAPPC9 intellectual disability gene. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/74600

16. C. Castronovo. RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING.

Degree: 2013, Università degli Studi di Milano

 Autistic behaviors were independently identified as recognizable syndromes in the early 20th century by Heller and, subsequently, by Kanner and Asperger. The autism diagnosis spans… (more)

Subjects/Keywords: autism spectrum disorders; copy number variations; array CGH; Settore MED/03 - Genetica Medica

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APA (6th Edition):

Castronovo, C. (2013). RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/218987

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):

Castronovo, C.. “RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING.” 2013. Thesis, Università degli Studi di Milano. Accessed October 28, 2020. http://hdl.handle.net/2434/218987.

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

MLA Handbook (7th Edition):

Castronovo, C.. “RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING.” 2013. Web. 28 Oct 2020.

Vancouver:

Castronovo C. RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2434/218987.

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

Council of Science Editors:

Castronovo C. RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/218987

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


University of Texas Southwestern Medical Center

17. Eskiocak, Banu. Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma.

Degree: 2016, University of Texas Southwestern Medical Center

 Genomic diversity and adaptive plasticity of melanoma tumors limit durable control with conventional and targeted therapies. Nevertheless, pathological activation of the ERK1/2 regulatory system is… (more)

Subjects/Keywords: Biomarkers; DNA Copy Number Variations; MAP Kinase Signaling System; Melanoma; Skin Neoplasms

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APA (6th Edition):

Eskiocak, B. (2016). Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5733

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):

Eskiocak, Banu. “Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed October 28, 2020. http://hdl.handle.net/2152.5/5733.

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

MLA Handbook (7th Edition):

Eskiocak, Banu. “Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma.” 2016. Web. 28 Oct 2020.

Vancouver:

Eskiocak B. Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2152.5/5733.

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

Council of Science Editors:

Eskiocak B. Biomarker Accessible and Chemically Addressable Mechanistic Subtypes of BRAF Melanoma. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5733

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


North-West University

18. Herfurth, Chanell. Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth .

Degree: 2014, North-West University

 Humans are continuously challenged by harmful endogenous and xenobiotic substances. Detoxification is the ability to neutralise and remove these substances from the body. Glycine N-acyltransferase,… (more)

Subjects/Keywords: GLYAT; Detoxification; Genetic variations; SNP; Copy number variance; Detoksifikasie; Genetiese variasies; Kopiegetal afwyking

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APA (6th Edition):

Herfurth, C. (2014). Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth . (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/11036

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):

Herfurth, Chanell. “Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth .” 2014. Thesis, North-West University. Accessed October 28, 2020. http://hdl.handle.net/10394/11036.

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

MLA Handbook (7th Edition):

Herfurth, Chanell. “Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth .” 2014. Web. 28 Oct 2020.

Vancouver:

Herfurth C. Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth . [Internet] [Thesis]. North-West University; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10394/11036.

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

Council of Science Editors:

Herfurth C. Sequencing and molecular characterization of variations in the glycine N-acyltransferase gene / Chanell Herfurth . [Thesis]. North-West University; 2014. Available from: http://hdl.handle.net/10394/11036

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


Freie Universität Berlin

19. Kariminejad, Roxana. Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen.

Degree: 2012, Freie Universität Berlin

 Die richtige räumliche und zeitliche Expression struktureller und regulatorischer Gene ist für die Hirnentwicklung von essentieller Bedeutung. Als Beitrag zur Aufklärung der daran beteiligten Mechanismen… (more)

Subjects/Keywords: Copy Number Variations; Brain Malformations; Array CGH; CNV; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Kariminejad, R. (2012). Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-11951

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):

Kariminejad, Roxana. “Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen.” 2012. Thesis, Freie Universität Berlin. Accessed October 28, 2020. http://dx.doi.org/10.17169/refubium-11951.

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

MLA Handbook (7th Edition):

Kariminejad, Roxana. “Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen.” 2012. Web. 28 Oct 2020.

Vancouver:

Kariminejad R. Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Oct 28]. Available from: http://dx.doi.org/10.17169/refubium-11951.

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

Council of Science Editors:

Kariminejad R. Copy-Number-Variations (CNVs) in der Ätiologie von Hirnfehlbildungen. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-11951

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


Tartu University

20. Palta, Priit. Computational methods for DNA copy number detection .

Degree: 2015, Tartu University

 DNA koopiaarvu variantideks või muutusteks nimetatakse selliseid erinevusi inimeste geneetilises materjalis, mille puhul mingi DNA lõigu koopiaarv on erinev oodatavast koopiaarvust kaks (üks koopia mingit… (more)

Subjects/Keywords: DNA koopiaarvu variatsioonid; genoomid; arvutusmeetodid; bioinformaatika; DNA copy number variations; genomes; numerical methods; bioinformatics

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APA (6th Edition):

Palta, P. (2015). Computational methods for DNA copy number detection . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/48509

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):

Palta, Priit. “Computational methods for DNA copy number detection .” 2015. Thesis, Tartu University. Accessed October 28, 2020. http://hdl.handle.net/10062/48509.

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

MLA Handbook (7th Edition):

Palta, Priit. “Computational methods for DNA copy number detection .” 2015. Web. 28 Oct 2020.

Vancouver:

Palta P. Computational methods for DNA copy number detection . [Internet] [Thesis]. Tartu University; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10062/48509.

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

Council of Science Editors:

Palta P. Computational methods for DNA copy number detection . [Thesis]. Tartu University; 2015. Available from: http://hdl.handle.net/10062/48509

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

21. Cheroki, Carola. Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins.

Degree: PhD, Biologia (Genética), 2008, University of São Paulo

 Introdução: A síndrome ou seqüência malformativa de Rokitansky-Mayer-Küster-Hauser (SR), de caráter geralmente esporádico, caracteriza-se por aplasia útero-vaginal, freqüentemente associada a anomalias esqueléticas e do trato… (more)

Subjects/Keywords: Absent or rudimentary uterus; Anomalias cromossômicas submicroscópicas; Aplasia útero vaginal; Array-CGH; Copy number variation (CNVs); Expressividade variável; Genomic imbalances; Short vagina

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APA (6th Edition):

Cheroki, C. (2008). Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-03062008-130845/ ;

Chicago Manual of Style (16th Edition):

Cheroki, Carola. “Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins.” 2008. Doctoral Dissertation, University of São Paulo. Accessed October 28, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-03062008-130845/ ;.

MLA Handbook (7th Edition):

Cheroki, Carola. “Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins.” 2008. Web. 28 Oct 2020.

Vancouver:

Cheroki C. Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Oct 28]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-03062008-130845/ ;.

Council of Science Editors:

Cheroki C. Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-03062008-130845/ ;


Universitat Pompeu Fabra

22. Spataro, Nino, 1984-. Human genetic disorders: Mendelian and complex diseases.

Degree: Departament de Ciències Experimentals i de la Salut, 2016, Universitat Pompeu Fabra

 Des de l'Origen de les Espècies de Darwin van passar molts anys abans que les malalties humanes fossin considerades sota un marc evolutiu. Tanmateix, tot… (more)

Subjects/Keywords: Mendelian disorders; Complex diseases; Parkinson's disease; Malalties complexes; Malaltia de Parkinson; Mètodes de col.lapse; Copy number variation (CNVs); Malalties mendelianes; Collapsing methods; Variació en el número de còpies; 575

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APA (6th Edition):

Spataro, Nino, 1. (2016). Human genetic disorders: Mendelian and complex diseases. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/482220

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):

Spataro, Nino, 1984-. “Human genetic disorders: Mendelian and complex diseases.” 2016. Thesis, Universitat Pompeu Fabra. Accessed October 28, 2020. http://hdl.handle.net/10803/482220.

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

MLA Handbook (7th Edition):

Spataro, Nino, 1984-. “Human genetic disorders: Mendelian and complex diseases.” 2016. Web. 28 Oct 2020.

Vancouver:

Spataro, Nino 1. Human genetic disorders: Mendelian and complex diseases. [Internet] [Thesis]. Universitat Pompeu Fabra; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10803/482220.

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

Council of Science Editors:

Spataro, Nino 1. Human genetic disorders: Mendelian and complex diseases. [Thesis]. Universitat Pompeu Fabra; 2016. Available from: http://hdl.handle.net/10803/482220

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


Penn State University

23. Khan, Hossain. Exploring Sequence Architectures at Flanking Regions of Copy Number Variants.

Degree: 2019, Penn State University

Copy number variations (CNVs) represent a subtype of structural variations where a portion of the genome is deleted or duplicated resulting in copy number changes… (more)

Subjects/Keywords: CNVs; Structural Variations; Alu elements; L1 LINE elements; Flanking regions of CNVs; Segmental Duplications

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APA (6th Edition):

Khan, H. (2019). Exploring Sequence Architectures at Flanking Regions of Copy Number Variants. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17031hmk42

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):

Khan, Hossain. “Exploring Sequence Architectures at Flanking Regions of Copy Number Variants.” 2019. Thesis, Penn State University. Accessed October 28, 2020. https://submit-etda.libraries.psu.edu/catalog/17031hmk42.

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

MLA Handbook (7th Edition):

Khan, Hossain. “Exploring Sequence Architectures at Flanking Regions of Copy Number Variants.” 2019. Web. 28 Oct 2020.

Vancouver:

Khan H. Exploring Sequence Architectures at Flanking Regions of Copy Number Variants. [Internet] [Thesis]. Penn State University; 2019. [cited 2020 Oct 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/17031hmk42.

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

Council of Science Editors:

Khan H. Exploring Sequence Architectures at Flanking Regions of Copy Number Variants. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/17031hmk42

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

24. Ribeiro, Cintia Marques. Estudo de genes candidatos aos Transtornos do Espectro Autista.

Degree: PhD, Biologia (Genética), 2013, University of São Paulo

 Os transtornos do espectro autista (TEA) são condições neuropsiquiátricas caracterizadas por padrões comportamentais estereotipados, ausência ou limitação de comunicação verbal e de interação social recíproca.… (more)

Subjects/Keywords: Autism spectrum disorders; Copy number variations; Microarray-CGH; Microarrays-CGH; Transtornos do espectro autista; Variações no número de cópias

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

APA (6th Edition):

Ribeiro, C. M. (2013). Estudo de genes candidatos aos Transtornos do Espectro Autista. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-06092013-153442/ ;

Chicago Manual of Style (16th Edition):

Ribeiro, Cintia Marques. “Estudo de genes candidatos aos Transtornos do Espectro Autista.” 2013. Doctoral Dissertation, University of São Paulo. Accessed October 28, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-06092013-153442/ ;.

MLA Handbook (7th Edition):

Ribeiro, Cintia Marques. “Estudo de genes candidatos aos Transtornos do Espectro Autista.” 2013. Web. 28 Oct 2020.

Vancouver:

Ribeiro CM. Estudo de genes candidatos aos Transtornos do Espectro Autista. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2020 Oct 28]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-06092013-153442/ ;.

Council of Science Editors:

Ribeiro CM. Estudo de genes candidatos aos Transtornos do Espectro Autista. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-06092013-153442/ ;

25. DeConti, Derrick K. Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation.

Degree: Interdisciplinary Graduate Program, Medicine, 2015, U of Massachusetts : Med

  Duplications and deletions are a major source of genomic variation. Duplications, specifically, have a significant impact on gene genesis and dosage, and the malaria… (more)

Subjects/Keywords: Plasmodium falciparum; Gene Duplication; Genomic Segmental Duplications; DNA Copy Number Variations; Bioinformatics; Computational Biology; Genetics; Genomics

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

APA (6th Edition):

DeConti, D. K. (2015). Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/869

Chicago Manual of Style (16th Edition):

DeConti, Derrick K. “Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 28, 2020. http://escholarship.umassmed.edu/gsbs_diss/869.

MLA Handbook (7th Edition):

DeConti, Derrick K. “Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation.” 2015. Web. 28 Oct 2020.

Vancouver:

DeConti DK. Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2020 Oct 28]. Available from: http://escholarship.umassmed.edu/gsbs_diss/869.

Council of Science Editors:

DeConti DK. Systematic Analysis of Duplications and Deletions in the Malaria Parasite P. falciparum: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/869


Universidade Estadual de Campinas

26. Martin, Nailú Angélica Sinicato, 1989-. Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus.

Degree: 2017, Universidade Estadual de Campinas

 Abstract: Systemic lupus erythematosus (SLE) is an autoimmune disease with a great spectrum of signs and symptoms that may arise according to the affected organ.… (more)

Subjects/Keywords: Lúpus eritematoso sistêmico; Hereditariedade; Variações do número de cópias de DNA; Lupus erythematosus, Systemic; Heredity; DNA copy number variations

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

APA (6th Edition):

Martin, Nailú Angélica Sinicato, 1. (2017). Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/322293

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):

Martin, Nailú Angélica Sinicato, 1989-. “Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus.” 2017. Thesis, Universidade Estadual de Campinas. Accessed October 28, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/322293.

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

MLA Handbook (7th Edition):

Martin, Nailú Angélica Sinicato, 1989-. “Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus.” 2017. Web. 28 Oct 2020.

Vancouver:

Martin, Nailú Angélica Sinicato 1. Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus. [Internet] [Thesis]. Universidade Estadual de Campinas; 2017. [cited 2020 Oct 28]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/322293.

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

Council of Science Editors:

Martin, Nailú Angélica Sinicato 1. Variações no número de cópias do DNA e recorrência familiar em pacientes com lúpus eritematoso sistêmico juvenil: DNA copy number variations and familiar recurrence in patients with childhood onset systemic lupus erythematosus. [Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/322293

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


Tartu University

27. Männik, Katrin. Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population .

Degree: 2012, Tartu University

 Intellektipuue on raske arenguhäire, mis arenenud riikides esineb ligikaudse sagedusega 2% üldpopulatsioonist. Intellektipuude tekkepõhjused võivad olla väga erinevad ning ligi pooltel patsientidest on häire põhjus… (more)

Subjects/Keywords: vaimne alaareng; DNA koopiaarvu variatsioonid; geeniuuringud; kromosoomid; populatsioonigeneetika; mental retardation; DNA copy number variations; genetic research; chromosomes; population genetics

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

APA (6th Edition):

Männik, K. (2012). Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/26095

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):

Männik, Katrin. “Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population .” 2012. Thesis, Tartu University. Accessed October 28, 2020. http://hdl.handle.net/10062/26095.

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

MLA Handbook (7th Edition):

Männik, Katrin. “Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population .” 2012. Web. 28 Oct 2020.

Vancouver:

Männik K. Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population . [Internet] [Thesis]. Tartu University; 2012. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10062/26095.

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

Council of Science Editors:

Männik K. Exploring the genomics of cognitive impairment: whole-genome SNP genotyping experience in Estonian patients and general population . [Thesis]. Tartu University; 2012. Available from: http://hdl.handle.net/10062/26095

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

28. La Cognata, Valentina. Reading through the building blocks of the genome: exonic variation in parkinson's disease.

Degree: 2017, Università degli Studi di Catania

 Parkinson's disease (PD) is one of the most common movement disorders worldwide, characterized by a profound and selective loss of dopaminergic neurons in the substantia… (more)

Subjects/Keywords: Area 06 - Scienze mediche; Genomics, Exons, Genes, Parkinson's Disease, Copy Number Variations, Alternative splicing, Systems biology

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

APA (6th Edition):

La Cognata, V. (2017). Reading through the building blocks of the genome: exonic variation in parkinson's disease. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/3927

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):

La Cognata, Valentina. “Reading through the building blocks of the genome: exonic variation in parkinson's disease.” 2017. Thesis, Università degli Studi di Catania. Accessed October 28, 2020. http://hdl.handle.net/10761/3927.

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

MLA Handbook (7th Edition):

La Cognata, Valentina. “Reading through the building blocks of the genome: exonic variation in parkinson's disease.” 2017. Web. 28 Oct 2020.

Vancouver:

La Cognata V. Reading through the building blocks of the genome: exonic variation in parkinson's disease. [Internet] [Thesis]. Università degli Studi di Catania; 2017. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10761/3927.

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

Council of Science Editors:

La Cognata V. Reading through the building blocks of the genome: exonic variation in parkinson's disease. [Thesis]. Università degli Studi di Catania; 2017. Available from: http://hdl.handle.net/10761/3927

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


Leiden University

29. Kriek, M. The human genome; you gain some, you lose some.

Degree: 2007, Leiden University

Copy number variations (CNVs) in the human genome are inherent in both evolutionary progression as well as the etiology of disease. The introduction of this… (more)

Subjects/Keywords: congenital malformation; Copy number variations; Evolutionary progression; Mental retardation; Pathogenicity; congenital malformation; Copy number variations; Evolutionary progression; Mental retardation; Pathogenicity

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

APA (6th Edition):

Kriek, M. (2007). The human genome; you gain some, you lose some. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/12479

Chicago Manual of Style (16th Edition):

Kriek, M. “The human genome; you gain some, you lose some.” 2007. Doctoral Dissertation, Leiden University. Accessed October 28, 2020. http://hdl.handle.net/1887/12479.

MLA Handbook (7th Edition):

Kriek, M. “The human genome; you gain some, you lose some.” 2007. Web. 28 Oct 2020.

Vancouver:

Kriek M. The human genome; you gain some, you lose some. [Internet] [Doctoral dissertation]. Leiden University; 2007. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1887/12479.

Council of Science Editors:

Kriek M. The human genome; you gain some, you lose some. [Doctoral Dissertation]. Leiden University; 2007. Available from: http://hdl.handle.net/1887/12479


University of Utah

30. 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

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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 October 28, 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. 28 Oct 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 Oct 28]. 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

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