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You searched for subject:(CNV). Showing records 1 – 30 of 104 total matches.

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Texas A&M University

1. Ghosh, Sharmila. Study of Genomic Copy Number Variation in Equine Health and Disease.

Degree: PhD, Biomedical Sciences, 2014, Texas A&M University

 This is a study of copy number variations (CNVs) in the horse genome to gain knowledge about the role of CNVs in equine biology, and… (more)

Subjects/Keywords: CNV; CNVR; RAO; DSD

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APA (6th Edition):

Ghosh, S. (2014). Study of Genomic Copy Number Variation in Equine Health and Disease. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153432

Chicago Manual of Style (16th Edition):

Ghosh, Sharmila. “Study of Genomic Copy Number Variation in Equine Health and Disease.” 2014. Doctoral Dissertation, Texas A&M University. Accessed December 01, 2020. http://hdl.handle.net/1969.1/153432.

MLA Handbook (7th Edition):

Ghosh, Sharmila. “Study of Genomic Copy Number Variation in Equine Health and Disease.” 2014. Web. 01 Dec 2020.

Vancouver:

Ghosh S. Study of Genomic Copy Number Variation in Equine Health and Disease. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1969.1/153432.

Council of Science Editors:

Ghosh S. Study of Genomic Copy Number Variation in Equine Health and Disease. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153432

2. Bonnefond, Mathilde. Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences.

Degree: Docteur es, Sciences Cognitives (doctorat sciences cognitives mention linguistique), 2009, Université Lumière – Lyon II

Le raisonnement conditionnel, fondé sur les énoncés de la forme Si P alors Q, est celui qui a reçu le plus d'attention de la part… (more)

Subjects/Keywords: N2; p3; psw; cnv

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APA (6th Edition):

Bonnefond, M. (2009). Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences. (Doctoral Dissertation). Université Lumière – Lyon II. Retrieved from http://www.theses.fr/2009LYO20101

Chicago Manual of Style (16th Edition):

Bonnefond, Mathilde. “Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences.” 2009. Doctoral Dissertation, Université Lumière – Lyon II. Accessed December 01, 2020. http://www.theses.fr/2009LYO20101.

MLA Handbook (7th Edition):

Bonnefond, Mathilde. “Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences.” 2009. Web. 01 Dec 2020.

Vancouver:

Bonnefond M. Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences. [Internet] [Doctoral dissertation]. Université Lumière – Lyon II; 2009. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2009LYO20101.

Council of Science Editors:

Bonnefond M. Caractérisation des étapes de traitement élémentaire du raisonnement conditionnel à l’aide de l’EEG et de la MEG : effet de l’incertitude du conditionnel et des différences interindividuelles : Characterization of elementary processing steps of conditional reasoning using EEG and MEG : effect of uncertainty of the conditional and individual differences. [Doctoral Dissertation]. Université Lumière – Lyon II; 2009. Available from: http://www.theses.fr/2009LYO20101


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

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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 01, 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. 01 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 01]. 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


West Virginia University

4. Singh, Salvi. Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations.

Degree: MS, Lane Department of Computer Science and Electrical Engineering, 2019, West Virginia University

  Lung cancer is the leading cause of cancer-related death in the world. Lung cancer can be categorized as non-small cell lung cancer (NSCLC) and… (more)

Subjects/Keywords: Boolean Implication Networks; DNA CNV; Genet-CNV; Bioinformatics; Other Computer Engineering

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APA (6th Edition):

Singh, S. (2019). Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations. (Thesis). West Virginia University. Retrieved from https://doi.org/10.33915/etd.3766 ; https://researchrepository.wvu.edu/etd/3766

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):

Singh, Salvi. “Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations.” 2019. Thesis, West Virginia University. Accessed December 01, 2020. https://doi.org/10.33915/etd.3766 ; https://researchrepository.wvu.edu/etd/3766.

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

MLA Handbook (7th Edition):

Singh, Salvi. “Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations.” 2019. Web. 01 Dec 2020.

Vancouver:

Singh S. Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations. [Internet] [Thesis]. West Virginia University; 2019. [cited 2020 Dec 01]. Available from: https://doi.org/10.33915/etd.3766 ; https://researchrepository.wvu.edu/etd/3766.

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

Council of Science Editors:

Singh S. Genet-CNV: Boolean Implication Networks for Modeling Genome-Wide Co-occurrence of DNA Copy Number Variations. [Thesis]. West Virginia University; 2019. Available from: https://doi.org/10.33915/etd.3766 ; https://researchrepository.wvu.edu/etd/3766

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

5. Sakai, Miwako. Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価.

Degree: 博士(医学), 2015, Niigata University / 新潟大学

学位の種類: 博士(医学). 報告番号: 甲第4063号. 学位記番号: 新大院博(医)甲第652号. 学位授与年月日: 平成27年9月24日

Molecular Cytogenetics. 2015, 8, 46.

Background: Cytogenomic mutations and chromosomal abnormality are implicated in the neuropathology of… (more)

Subjects/Keywords: CNV; Caudate; Genome instability; Schizophrenia; Somatic mutation

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APA (6th Edition):

Sakai, M. (2015). Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価. (Thesis). Niigata University / 新潟大学. Retrieved from http://hdl.handle.net/10191/35555

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):

Sakai, Miwako. “Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価.” 2015. Thesis, Niigata University / 新潟大学. Accessed December 01, 2020. http://hdl.handle.net/10191/35555.

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

MLA Handbook (7th Edition):

Sakai, Miwako. “Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価.” 2015. Web. 01 Dec 2020.

Vancouver:

Sakai M. Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価. [Internet] [Thesis]. Niigata University / 新潟大学; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10191/35555.

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

Council of Science Editors:

Sakai M. Assessment of copy number variations in the brain genome of schizophrenia patients : 統合失調症患者の脳内ゲノムにおけるコピー数変異の評価. [Thesis]. Niigata University / 新潟大学; 2015. Available from: http://hdl.handle.net/10191/35555

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


University of Toronto

6. Kanji, Zaheer Shamshudin. Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery.

Degree: 2013, University of Toronto

Familial Pancreatic Cancer (FPC) is an autosomal dominant condition with greater then 80% of genetic causes unknown. We hypothesize that an integrative approach employing germline… (more)

Subjects/Keywords: Cancer; Pancreatic; CNV; Genomics; Exome; Sequencing; 0564

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APA (6th Edition):

Kanji, Z. S. (2013). Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42995

Chicago Manual of Style (16th Edition):

Kanji, Zaheer Shamshudin. “Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery.” 2013. Masters Thesis, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/42995.

MLA Handbook (7th Edition):

Kanji, Zaheer Shamshudin. “Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery.” 2013. Web. 01 Dec 2020.

Vancouver:

Kanji ZS. Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/42995.

Council of Science Editors:

Kanji ZS. Somatic Copy Number Aberrations in Familial Pancreatic Cancer: Integrative Genomics and Gene Discovery. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42995


Boston University

7. Park, Richard Won. Visualization and analysis of cancer genome sequencing studies.

Degree: PhD, Bioinformatics, 2014, Boston University

 Large-scale genomics projects such as the Cancer Genome Atlas (TCGA), and the Encyclopedia of DNA Elements (ENCODE) involve generation of data at an unprecedented scale,… (more)

Subjects/Keywords: Bioinformatics; Cancer; CNV; NGS; Sequencing; Visualization

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APA (6th Edition):

Park, R. W. (2014). Visualization and analysis of cancer genome sequencing studies. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15066

Chicago Manual of Style (16th Edition):

Park, Richard Won. “Visualization and analysis of cancer genome sequencing studies.” 2014. Doctoral Dissertation, Boston University. Accessed December 01, 2020. http://hdl.handle.net/2144/15066.

MLA Handbook (7th Edition):

Park, Richard Won. “Visualization and analysis of cancer genome sequencing studies.” 2014. Web. 01 Dec 2020.

Vancouver:

Park RW. Visualization and analysis of cancer genome sequencing studies. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2144/15066.

Council of Science Editors:

Park RW. Visualization and analysis of cancer genome sequencing studies. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15066


University of Washington

8. Rippey, Caitlin Fields. Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia.

Degree: PhD, 2013, University of Washington

 Chimeric genes are caused by structural genomic rearrangements that fuse together portions of two different genes to create a novel gene. Chimeras may differ from… (more)

Subjects/Keywords: Chimerism; CNV; Schizophrenia; Genetics; Mental health; genetics

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APA (6th Edition):

Rippey, C. F. (2013). Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/23452

Chicago Manual of Style (16th Edition):

Rippey, Caitlin Fields. “Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia.” 2013. Doctoral Dissertation, University of Washington. Accessed December 01, 2020. http://hdl.handle.net/1773/23452.

MLA Handbook (7th Edition):

Rippey, Caitlin Fields. “Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia.” 2013. Web. 01 Dec 2020.

Vancouver:

Rippey CF. Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1773/23452.

Council of Science Editors:

Rippey CF. Formation of Chimeric Genes by Copy Number Variation as a Mutational Mechanism in Schizophrenia. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/23452


University of Sydney

9. Martin La Rotta, Nancy Yamile Del Pilar. Comparative analysis of chromosome 8 copy number in paediatric solid tumours .

Degree: 2015, University of Sydney

 Chromosomal imbalances are of major significance in cancer initiation and progression. Gains of chromosome 8 in human cancer have been described by a number of… (more)

Subjects/Keywords: aCGH; MLPA; CNV; solid tumours; cancer

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APA (6th Edition):

Martin La Rotta, N. Y. D. P. (2015). Comparative analysis of chromosome 8 copy number in paediatric solid tumours . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16185

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 La Rotta, Nancy Yamile Del Pilar. “Comparative analysis of chromosome 8 copy number in paediatric solid tumours .” 2015. Thesis, University of Sydney. Accessed December 01, 2020. http://hdl.handle.net/2123/16185.

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

MLA Handbook (7th Edition):

Martin La Rotta, Nancy Yamile Del Pilar. “Comparative analysis of chromosome 8 copy number in paediatric solid tumours .” 2015. Web. 01 Dec 2020.

Vancouver:

Martin La Rotta NYDP. Comparative analysis of chromosome 8 copy number in paediatric solid tumours . [Internet] [Thesis]. University of Sydney; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2123/16185.

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

Council of Science Editors:

Martin La Rotta NYDP. Comparative analysis of chromosome 8 copy number in paediatric solid tumours . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/16185

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

10. Tessereau, Chloé. Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition.

Degree: Docteur es, Biologie, 2014, Université Claude Bernard – Lyon I

Le macrosatellite RNU2 est constitué de répétitions en tandem d'une unité de 6,1 kb. Largement étudié pendant les années 1980 et 1990, il est maintenant… (more)

Subjects/Keywords: RNU2; Macrosatellite; CNV; BRCA1; Cancer du sein; RNU2; Macrosatellite; CNV; BRCA1; Breast cancer; 616.994

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APA (6th Edition):

Tessereau, C. (2014). Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2014LYO10075

Chicago Manual of Style (16th Edition):

Tessereau, Chloé. “Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition.” 2014. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed December 01, 2020. http://www.theses.fr/2014LYO10075.

MLA Handbook (7th Edition):

Tessereau, Chloé. “Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition.” 2014. Web. 01 Dec 2020.

Vancouver:

Tessereau C. Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2014. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2014LYO10075.

Council of Science Editors:

Tessereau C. Le macrosatellite RNU2 : caractérisation, évolution et lien avec la prédisposition génétique au cancer du sein : The RNU2 macrosatellite : characterization, evolution and link with breast cancer genetic predisposition. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2014. Available from: http://www.theses.fr/2014LYO10075

11. Bitar, Tania. Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université François-Rabelais de Tours

L’étiologie des troubles du spectre autistique (TSA) est multifactorielle mettant en jeu une forte composante génétique ainsi que des facteurs environnementaux. A ce jour, il… (more)

Subjects/Keywords: TSA; Environnement; CGHarray; CNV; Métabolomique; Urine; Biomarqueurs; ASD; Environment; CGHarray; CNV; Metabolomics; Urine; Biomarkers

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APA (6th Edition):

Bitar, T. (2018). Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2018TOUR3307

Chicago Manual of Style (16th Edition):

Bitar, Tania. “Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon.” 2018. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed December 01, 2020. http://www.theses.fr/2018TOUR3307.

MLA Handbook (7th Edition):

Bitar, Tania. “Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon.” 2018. Web. 01 Dec 2020.

Vancouver:

Bitar T. Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2018. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2018TOUR3307.

Council of Science Editors:

Bitar T. Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban : Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2018. Available from: http://www.theses.fr/2018TOUR3307

12. Uehara, Daniela Tiaki. Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica.

Degree: Mestrado, Biologia (Genética), 2010, University of São Paulo

 A complexidade da fisiologia da audição resulta da participação e interação de produtos de grande número de genes, razão pela qual a surdez hereditária exibe… (more)

Subjects/Keywords: CNV; CNV; Hereditary deafness; MLPA; MLPA; Nonsyndromic deafness; Surdez hereditária; Surdez não-sindrômica; Surdez sindrômica; Syndromic deafness

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APA (6th Edition):

Uehara, D. T. (2010). Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-22022011-111240/ ;

Chicago Manual of Style (16th Edition):

Uehara, Daniela Tiaki. “Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica.” 2010. Masters Thesis, University of São Paulo. Accessed December 01, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-22022011-111240/ ;.

MLA Handbook (7th Edition):

Uehara, Daniela Tiaki. “Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica.” 2010. Web. 01 Dec 2020.

Vancouver:

Uehara DT. Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Dec 01]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-22022011-111240/ ;.

Council of Science Editors:

Uehara DT. Pesquisa de microrrearranjos em genes candidatos a surdez sindrômica e não-sindrômica. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-22022011-111240/ ;

13. Rodrigues, Melina Guerreiro. Em busca da etiologia das displasias frontonasais.

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

 A displasia frontonasal (DFN) compreende quadros de aparência facial variável, sendo clinicamente caracterizada por dois ou mais dos seguintes sinais: hipertelorismo ocular com consequente alargamento… (more)

Subjects/Keywords: ALX1; ALX1; ALX4; ALX4; Candidate genes; CNV; CNV; Displasia frontonasal; Frontonasal dysplasia; Genes candidatos; Rearranjos cromossômicos estruturais; Structural chromosomal rearrangements

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APA (6th Edition):

Rodrigues, M. G. (2013). Em busca da etiologia das displasias frontonasais. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24032014-093037/ ;

Chicago Manual of Style (16th Edition):

Rodrigues, Melina Guerreiro. “Em busca da etiologia das displasias frontonasais.” 2013. Masters Thesis, University of São Paulo. Accessed December 01, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24032014-093037/ ;.

MLA Handbook (7th Edition):

Rodrigues, Melina Guerreiro. “Em busca da etiologia das displasias frontonasais.” 2013. Web. 01 Dec 2020.

Vancouver:

Rodrigues MG. Em busca da etiologia das displasias frontonasais. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2020 Dec 01]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24032014-093037/ ;.

Council of Science Editors:

Rodrigues MG. Em busca da etiologia das displasias frontonasais. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24032014-093037/ ;

14. Passot, Christophe. Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2014, Université François-Rabelais de Tours

Le FcRn est le récepteur responsable du recyclage des IgG ainsi que de leur transcytose. Ainsi cette protéine a un rôle majeur dans la pharmacocinétique… (more)

Subjects/Keywords: FcRn; Pharmacocinétique; Polymorphismes génétiques; Anticorps thérapeutiques; CNV; VNTR; Plaquettes; FcRn; Pharmacokinetics; Genetic polymorphisms; Therapeutic antibodies; CNV; Platelets

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APA (6th Edition):

Passot, C. (2014). Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2014TOUR3302

Chicago Manual of Style (16th Edition):

Passot, Christophe. “Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies.” 2014. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed December 01, 2020. http://www.theses.fr/2014TOUR3302.

MLA Handbook (7th Edition):

Passot, Christophe. “Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies.” 2014. Web. 01 Dec 2020.

Vancouver:

Passot C. Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2014. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2014TOUR3302.

Council of Science Editors:

Passot C. Expression du récepteur FcRn et pharmacocinétique des anticorps thérapeutiques : Expression of FcRn receptor and pharmacokinetics of monoclonal antibodies. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2014. Available from: http://www.theses.fr/2014TOUR3302

15. Karaouzene, Thomas. Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene.

Degree: Docteur es, MBS - Modèles, méthodes et algorithmes en biologie, santé et environnement, 2017, Université Grenoble Alpes (ComUE)

 Ces dix dernières années, l’investigation des maladies génétiques a été bouleversée par l’émergence des techniques de séquençage haut-débit. Celles-ci permettent désormais de ne plus séquencer… (more)

Subjects/Keywords: Séquençage Exomique; Algorithme; Infertilité; Variation du nombre de copie (CNV); Exome sequencing; Algorithm; Infertility; Copy number variation (CNV); 570; 004; 610

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APA (6th Edition):

Karaouzene, T. (2017). Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAS041

Chicago Manual of Style (16th Edition):

Karaouzene, Thomas. “Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed December 01, 2020. http://www.theses.fr/2017GREAS041.

MLA Handbook (7th Edition):

Karaouzene, Thomas. “Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene.” 2017. Web. 01 Dec 2020.

Vancouver:

Karaouzene T. Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2017GREAS041.

Council of Science Editors:

Karaouzene T. Bioinformatique et infertilité : analyse des données de séquençage haut-débit et caractérisation moléculaire du gène DPY19L2 : Bioinformatics and infertility : high throughput sequencing data analysis and molecular characterization of DPY19L2 gene. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAS041


Vrije Universiteit Amsterdam

16. Hazenbosch, P. Voor het volk om Christus' wil : Een geschiedenis van het CNV .

Degree: 2009, Vrije Universiteit Amsterdam

Subjects/Keywords: Geschiedenis CNV; cnv; sociale geschiedenis; christelijk-sociaal denken

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APA (6th Edition):

Hazenbosch, P. (2009). Voor het volk om Christus' wil : Een geschiedenis van het CNV . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/19797

Chicago Manual of Style (16th Edition):

Hazenbosch, P. “Voor het volk om Christus' wil : Een geschiedenis van het CNV .” 2009. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed December 01, 2020. http://hdl.handle.net/1871/19797.

MLA Handbook (7th Edition):

Hazenbosch, P. “Voor het volk om Christus' wil : Een geschiedenis van het CNV .” 2009. Web. 01 Dec 2020.

Vancouver:

Hazenbosch P. Voor het volk om Christus' wil : Een geschiedenis van het CNV . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2009. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1871/19797.

Council of Science Editors:

Hazenbosch P. Voor het volk om Christus' wil : Een geschiedenis van het CNV . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2009. Available from: http://hdl.handle.net/1871/19797


Brno University of Technology

17. Lacinová, Michaela. Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes.

Degree: 2019, Brno University of Technology

 This master thesis deals with analysis of structural variation of genome and with methods of its sequencing across all generations. Subsequently it contains a description… (more)

Subjects/Keywords: Variabilita počtu kopií; CNV; sekvenování; bakteriální genom; Klebsiella pneumoniae; Copy number variation; CNV; sequencing; bacterial genome; Klebsiella pneumoniae

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APA (6th Edition):

Lacinová, M. (2019). Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/177648

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):

Lacinová, Michaela. “Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes.” 2019. Thesis, Brno University of Technology. Accessed December 01, 2020. http://hdl.handle.net/11012/177648.

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

MLA Handbook (7th Edition):

Lacinová, Michaela. “Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes.” 2019. Web. 01 Dec 2020.

Vancouver:

Lacinová M. Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11012/177648.

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

Council of Science Editors:

Lacinová M. Detekce CNV v bakteriálních genomech: CNV detection in bacterial genomes. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/177648

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

18. Arista, Gautier. Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Université de Strasbourg

La vigne (Vitis vinifera) possède un métabolisme secondaire particulièrement riche donnant naissance à une large palette de molécules dont certaines sont impliquées dans les défenses… (more)

Subjects/Keywords: Vigne; Familles de gènes; Génomique comparative; Transcriptomique; CNV; Grapevine; Family of genes; Comparative genomics; Transcriptomics; CNV; 572.8; 581

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APA (6th Edition):

Arista, G. (2017). Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ010

Chicago Manual of Style (16th Edition):

Arista, Gautier. “Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed December 01, 2020. http://www.theses.fr/2017STRAJ010.

MLA Handbook (7th Edition):

Arista, Gautier. “Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives.” 2017. Web. 01 Dec 2020.

Vancouver:

Arista G. Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2017STRAJ010.

Council of Science Editors:

Arista G. Génomique comparative et fonctionnelle de familles de gènes liés au métabolisme secondaire de la vigne (Vitis vinifera) et de ses proches parents : Comparative and functional genomics of gene families linked to secondary metabolism in grapevine (Vitis vinifera) and its relatives. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ010

19. Huguet, Guillaume. Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia.

Degree: Docteur es, Génétique, 2013, Université Paris Descartes – Paris V

Les troubles du spectre autistique (TSA) touchent approximativement 1% de la population générale. Ces troubles se caractérisent par un déficit de la communication sociale, ainsi… (more)

Subjects/Keywords: Génétique; Dyslexie; Autisme; CNV; Synapse; Gènes; Mutations; Pression de sélection; Genetics; Dyslexia; Autism; CNV; Synapse; Genes; Mutations; Selection pressure; 599.935; 616.042

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

APA (6th Edition):

Huguet, G. (2013). Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T078

Chicago Manual of Style (16th Edition):

Huguet, Guillaume. “Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed December 01, 2020. http://www.theses.fr/2013PA05T078.

MLA Handbook (7th Edition):

Huguet, Guillaume. “Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia.” 2013. Web. 01 Dec 2020.

Vancouver:

Huguet G. Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2013PA05T078.

Council of Science Editors:

Huguet G. Identification de facteurs génétiques impliqués dans les troubles du spectre autistique et de la dyslexie : Identification of genetic factors involved in autism spectrum disorders and dyslexia. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T078


University of Michigan

20. Shen, Feichen. Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies.

Degree: PhD, Human Genetics, 2019, University of Michigan

 Copy number variation (CNV) is an important class of variation that contributes to genome evolution and disease. CNVs that become fixed in a species give… (more)

Subjects/Keywords: CNV; kmer; canine evolution; genome assembly; Genetics; Health Sciences

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

APA (6th Edition):

Shen, F. (2019). Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/150064

Chicago Manual of Style (16th Edition):

Shen, Feichen. “Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies.” 2019. Doctoral Dissertation, University of Michigan. Accessed December 01, 2020. http://hdl.handle.net/2027.42/150064.

MLA Handbook (7th Edition):

Shen, Feichen. “Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies.” 2019. Web. 01 Dec 2020.

Vancouver:

Shen F. Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2027.42/150064.

Council of Science Editors:

Shen F. Development of Copy Number Variation Detection Algorithms and Their Application to Genome Diversity Studies. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/150064

21. M.G. Strillacci. GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION.

Degree: 2014, Università degli Studi di Milano

 The QTL involved in susceptibility/resistance of infectious diseases and in the productive traits variations, are characterized by genetic heterogeneity and multifactorial inheritance, involving gene polymorphisms… (more)

Subjects/Keywords: gwas; cnv; bovine; Settore AGR/17 - Zootecnica Generale e Miglioramento Genetico

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APA (6th Edition):

Strillacci, M. (2014). GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/243633

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):

Strillacci, M.G.. “GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION.” 2014. Thesis, Università degli Studi di Milano. Accessed December 01, 2020. http://hdl.handle.net/2434/243633.

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

MLA Handbook (7th Edition):

Strillacci, M.G.. “GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION.” 2014. Web. 01 Dec 2020.

Vancouver:

Strillacci M. GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2434/243633.

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

Council of Science Editors:

Strillacci M. GENOME-WIDE DETECTION OF QTL AND CNVS IN DAIRY CATTLE POPULATION. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/243633

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


Colorado State University

22. Cabral, Brittany Kristine. Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The.

Degree: MS(M.S.), Human Development and Family Studies, 2014, Colorado State University

 The contingent negative variation (CNV) is a slow, negative drift in electroencephalographic potential that occurs between two stimuli. Researchers have examined the CNV and its… (more)

Subjects/Keywords: development; reliability; ERP; attention; contingent negative variation (CNV); EEG

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APA (6th Edition):

Cabral, B. K. (2014). Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/83880

Chicago Manual of Style (16th Edition):

Cabral, Brittany Kristine. “Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The.” 2014. Masters Thesis, Colorado State University. Accessed December 01, 2020. http://hdl.handle.net/10217/83880.

MLA Handbook (7th Edition):

Cabral, Brittany Kristine. “Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The.” 2014. Web. 01 Dec 2020.

Vancouver:

Cabral BK. Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The. [Internet] [Masters thesis]. Colorado State University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10217/83880.

Council of Science Editors:

Cabral BK. Test-retest reliability of the contingent negative variation (CNV) in children and adults before and after removing aberrant CNV segments, The. [Masters Thesis]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/83880


Université Paris-Sud – Paris XI

23. Marenne, Gaëlle. Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie.

Degree: Docteur es, Statistique génétique, 2012, Université Paris-Sud – Paris XI

Les variations en nombre de copies (CNV) sont des gains ou pertes d’une séquence d’ADN et peuvent avoir un rôle dans la susceptibilité à certaines… (more)

Subjects/Keywords: Variations en nombre de copies (CNV); Polymorphisme d’un seul nucléotide (SNP); Détection des CNV; Étude d’association pangénomique; Cancer de la vessie; Copy number variation (CNV); Single nucleotide polymorphism (SNP); CNV calling; Genomewide association study; Bladder cancer

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APA (6th Edition):

Marenne, G. (2012). Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA11T046

Chicago Manual of Style (16th Edition):

Marenne, Gaëlle. “Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 01, 2020. http://www.theses.fr/2012PA11T046.

MLA Handbook (7th Edition):

Marenne, Gaëlle. “Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie.” 2012. Web. 01 Dec 2020.

Vancouver:

Marenne G. Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2012PA11T046.

Council of Science Editors:

Marenne G. Statistical Methods to Combine SPN and CNV Information in Genome-Wide Association Studies : An Application to Bladder Cancer : Utilisation conjointe de l'information apportée par les différents polymorphismes, SNPs et CNVs, dans les études d'association pangénomique : application au cancer de la vessie. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA11T046


University of Western Ontario

24. Maiti, Sujit. Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia.

Degree: 2012, University of Western Ontario

 Genetic variability is essential to human individuality. Genetic variation includes differences in sequence at the single nucleotide level to structural variations of large segments of… (more)

Subjects/Keywords: Copy number variants; microarray; monozygotic twin; CNV calling algorithms; Life Sciences

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APA (6th Edition):

Maiti, S. (2012). Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1108

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):

Maiti, Sujit. “Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia.” 2012. Thesis, University of Western Ontario. Accessed December 01, 2020. https://ir.lib.uwo.ca/etd/1108.

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

MLA Handbook (7th Edition):

Maiti, Sujit. “Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia.” 2012. Web. 01 Dec 2020.

Vancouver:

Maiti S. Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2020 Dec 01]. Available from: https://ir.lib.uwo.ca/etd/1108.

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

Council of Science Editors:

Maiti S. Comprehensive Assessment of CNV Calling Algorithms: A Family Based Study Involving Monozygotic Twins Discordant for Schizophrenia. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/1108

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


Washington University in St. Louis

25. Lin, Peng. New methods for discovering common and rare genetic variants in human disease.

Degree: PhD, Biology and Biomedical Sciences: Human and Statistical Genetics, 2011, Washington University in St. Louis

 Since the discovery of Mendel's laws, one of the most challenging problems in genetic research has been to locate and characterize genetic variants that cause… (more)

Subjects/Keywords: Biostatistics; Genetics; Alcohol dependence; CNV accuracy; Collapsing; Imputation accuracy; Rare variants

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APA (6th Edition):

Lin, P. (2011). New methods for discovering common and rare genetic variants in human disease. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/606

Chicago Manual of Style (16th Edition):

Lin, Peng. “New methods for discovering common and rare genetic variants in human disease.” 2011. Doctoral Dissertation, Washington University in St. Louis. Accessed December 01, 2020. https://openscholarship.wustl.edu/etd/606.

MLA Handbook (7th Edition):

Lin, Peng. “New methods for discovering common and rare genetic variants in human disease.” 2011. Web. 01 Dec 2020.

Vancouver:

Lin P. New methods for discovering common and rare genetic variants in human disease. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2011. [cited 2020 Dec 01]. Available from: https://openscholarship.wustl.edu/etd/606.

Council of Science Editors:

Lin P. New methods for discovering common and rare genetic variants in human disease. [Doctoral Dissertation]. Washington University in St. Louis; 2011. Available from: https://openscholarship.wustl.edu/etd/606


Universidade do Rio Grande do Norte

26. Silva, Heglayne Pereira Vital da. Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina .

Degree: 2019, Universidade do Rio Grande do Norte

 Non-syndromic orofacial clefts (OFC) consist of craniofacial malformations characterized by the presence of abnormal spaces or gaps in the upper lip, alveolus and/or palate, which… (more)

Subjects/Keywords: Fenda de lábio e palato; Genética; CNV; Análise cromossômica por microarranjos

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APA (6th Edition):

Silva, H. P. V. d. (2019). Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina . (Doctoral Dissertation). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/28603

Chicago Manual of Style (16th Edition):

Silva, Heglayne Pereira Vital da. “Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina .” 2019. Doctoral Dissertation, Universidade do Rio Grande do Norte. Accessed December 01, 2020. http://repositorio.ufrn.br/handle/123456789/28603.

MLA Handbook (7th Edition):

Silva, Heglayne Pereira Vital da. “Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina .” 2019. Web. 01 Dec 2020.

Vancouver:

Silva HPVd. Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina . [Internet] [Doctoral dissertation]. Universidade do Rio Grande do Norte; 2019. [cited 2020 Dec 01]. Available from: http://repositorio.ufrn.br/handle/123456789/28603.

Council of Science Editors:

Silva HPVd. Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina . [Doctoral Dissertation]. Universidade do Rio Grande do Norte; 2019. Available from: http://repositorio.ufrn.br/handle/123456789/28603


University of Melbourne

27. Payne, Gemma Marie. Structural variations in the ovine genome: their detection and association with phenotypic traits.

Degree: 2013, University of Melbourne

 Growth and meat yield traits are important to the New Zealand sheep industry. Genomic selection (GS) of these traits uses information from high density ovine… (more)

Subjects/Keywords: CNV; sheep; genetics; genomics; association; SNP; meat yield; growth

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APA (6th Edition):

Payne, G. M. (2013). Structural variations in the ovine genome: their detection and association with phenotypic traits. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38589

Chicago Manual of Style (16th Edition):

Payne, Gemma Marie. “Structural variations in the ovine genome: their detection and association with phenotypic traits.” 2013. Doctoral Dissertation, University of Melbourne. Accessed December 01, 2020. http://hdl.handle.net/11343/38589.

MLA Handbook (7th Edition):

Payne, Gemma Marie. “Structural variations in the ovine genome: their detection and association with phenotypic traits.” 2013. Web. 01 Dec 2020.

Vancouver:

Payne GM. Structural variations in the ovine genome: their detection and association with phenotypic traits. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11343/38589.

Council of Science Editors:

Payne GM. Structural variations in the ovine genome: their detection and association with phenotypic traits. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38589

28. Dammers, Jürgen. Localisation and time courses of CMV generators from MFT analysis of average MEG signals.

Degree: PhD, 2000, Open University

 The research presented here is divided into two parts. The first part addresses questions relating to the localisation capability of magnetoencephalography (MEG), with emphasise on… (more)

Subjects/Keywords: 612; Magnetoencephalography; CNV; Motor cortex

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

APA (6th Edition):

Dammers, J. (2000). Localisation and time courses of CMV generators from MFT analysis of average MEG signals. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/63849/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326584

Chicago Manual of Style (16th Edition):

Dammers, Jürgen. “Localisation and time courses of CMV generators from MFT analysis of average MEG signals.” 2000. Doctoral Dissertation, Open University. Accessed December 01, 2020. http://oro.open.ac.uk/63849/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326584.

MLA Handbook (7th Edition):

Dammers, Jürgen. “Localisation and time courses of CMV generators from MFT analysis of average MEG signals.” 2000. Web. 01 Dec 2020.

Vancouver:

Dammers J. Localisation and time courses of CMV generators from MFT analysis of average MEG signals. [Internet] [Doctoral dissertation]. Open University; 2000. [cited 2020 Dec 01]. Available from: http://oro.open.ac.uk/63849/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326584.

Council of Science Editors:

Dammers J. Localisation and time courses of CMV generators from MFT analysis of average MEG signals. [Doctoral Dissertation]. Open University; 2000. Available from: http://oro.open.ac.uk/63849/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326584

29. Cintia Cristina Palu. CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano.

Degree: 2010, Laboratório Nacional de Computação Científica

 O uso de ferramentas de análise e visualização de dados é essencial para a pesquisa de CNVs, porém nem sempre está ao alcance de todo… (more)

Subjects/Keywords: Bioinformática; Desenvolvimento de Website,Informática na medicina; Computação gráfica; CNV-Variação do número de cópias; Comparação de perfil de CNV; Ánalise exploratória-Desenvolvimento de software; CIENCIAS BIOLOGICAS; CIENCIAS BIOLOGICAS

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

APA (6th Edition):

Palu, C. C. (2010). CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano. (Masters Thesis). Laboratório Nacional de Computação Científica. Retrieved from http://www.lncc.br/tdmc/tde_busca/arquivo.php?codArquivo=226

Chicago Manual of Style (16th Edition):

Palu, Cintia Cristina. “CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano.” 2010. Masters Thesis, Laboratório Nacional de Computação Científica. Accessed December 01, 2020. http://www.lncc.br/tdmc/tde_busca/arquivo.php?codArquivo=226.

MLA Handbook (7th Edition):

Palu, Cintia Cristina. “CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano.” 2010. Web. 01 Dec 2020.

Vancouver:

Palu CC. CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano. [Internet] [Masters thesis]. Laboratório Nacional de Computação Científica; 2010. [cited 2020 Dec 01]. Available from: http://www.lncc.br/tdmc/tde_busca/arquivo.php?codArquivo=226.

Council of Science Editors:

Palu CC. CNViewer : aplicativo baseado em navegador web para análise de variações de número de cópias (CNV) do genoma humano. [Masters Thesis]. Laboratório Nacional de Computação Científica; 2010. Available from: http://www.lncc.br/tdmc/tde_busca/arquivo.php?codArquivo=226


Brno University of Technology

30. Pleskačová, Barbora. Detekce CNV v sekvenačních datech: CNV detection in the sequencing data.

Degree: 2020, Brno University of Technology

 Copy number variation detection in prokaryotic organisms is currently receiving more and more attention, mainly due to the association of CNV with pathogenicity and antibiotic… (more)

Subjects/Keywords: Variabilita počtu kopií; CNV; strukturní variabilita; prokaryotní genom; sekvenační čtení; pokrytí; Copy number variation; CNV; structural variation; prokaryotic genome; sequencing reads; coverage

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

APA (6th Edition):

Pleskačová, B. (2020). Detekce CNV v sekvenačních datech: CNV detection in the sequencing data. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/189153

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):

Pleskačová, Barbora. “Detekce CNV v sekvenačních datech: CNV detection in the sequencing data.” 2020. Thesis, Brno University of Technology. Accessed December 01, 2020. http://hdl.handle.net/11012/189153.

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

MLA Handbook (7th Edition):

Pleskačová, Barbora. “Detekce CNV v sekvenačních datech: CNV detection in the sequencing data.” 2020. Web. 01 Dec 2020.

Vancouver:

Pleskačová B. Detekce CNV v sekvenačních datech: CNV detection in the sequencing data. [Internet] [Thesis]. Brno University of Technology; 2020. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11012/189153.

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

Council of Science Editors:

Pleskačová B. Detekce CNV v sekvenačních datech: CNV detection in the sequencing data. [Thesis]. Brno University of Technology; 2020. Available from: http://hdl.handle.net/11012/189153

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

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