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Refinado por: assunto: Genome, Human remover
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31
Clustering of codons with rare cognate tRNAs in human genes suggests an extra level of expression regulation
Clustering of codons with rare cognate tRNAs in human genes suggests an extra level of expression regulation
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Clustering of codons with rare cognate tRNAs in human genes suggests an extra level of expression regulation

Parmley, Joanna L ; Huynen, Martijn A Petrov, Dmitri A.

PLoS genetics, 2009-07, Vol.5 (7), p.e1000548-e1000548 [Periódico revisado por pares]

United States: Public Library of Science

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32
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
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Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Zhou, Bo ; Ho, Steve S ; Zhang, Xianglong ; Pattni, Reenal ; Haraksingh, Rajini R ; Urban, Alexander E

Journal of medical genetics, 2018-11, Vol.55 (11), p.735-743 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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33
BFAST: an alignment tool for large scale genome resequencing
BFAST: an alignment tool for large scale genome resequencing
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BFAST: an alignment tool for large scale genome resequencing

Homer, Nils ; Merriman, Barry ; Nelson, Stanley F Creighton, Chad

PloS one, 2009-11, Vol.4 (11), p.e7767-e7767 [Periódico revisado por pares]

United States: Public Library of Science

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34
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization
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Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

Blout Zawatsky, Carrie L. ; Shah, Nidhi ; Machini, Kalotina ; Perez, Emma ; Christensen, Kurt D. ; Zouk, Hana ; Steeves, Marcie ; Koch, Christopher ; Uveges, Melissa ; Shea, Janelle ; Gold, Nina ; Krier, Joel ; Boutin, Natalie ; Mahanta, Lisa ; Rehm, Heidi L. ; Weiss, Scott T. ; Karlson, Elizabeth W. ; Smoller, Jordan W. ; Lebo, Matthew S. ; Green, Robert C.

American journal of human genetics, 2021-12, Vol.108 (12), p.2224-2237 [Periódico revisado por pares]

United States: Elsevier Inc

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35
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
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Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

Pasaniuc, Bogdan ; Zaitlen, Noah ; Lettre, Guillaume ; Chen, Gary K ; Tandon, Arti ; Kao, W H Linda ; Ruczinski, Ingo ; Fornage, Myriam ; Siscovick, David S ; Zhu, Xiaofeng ; Larkin, Emma ; Lange, Leslie A ; Cupples, L Adrienne ; Yang, Qiong ; Akylbekova, Ermeg L ; Musani, Solomon K ; Divers, Jasmin ; Mychaleckyj, Joe ; Li, Mingyao ; Papanicolaou, George J ; Millikan, Robert C ; Ambrosone, Christine B ; John, Esther M ; Bernstein, Leslie ; Zheng, Wei ; Hu, Jennifer J ; Ziegler, Regina G ; Nyante, Sarah J ; Bandera, Elisa V ; Ingles, Sue A ; Press, Michael F ; Chanock, Stephen J ; Deming, Sandra L ; Rodriguez-Gil, Jorge L ; Palmer, Cameron D ; Buxbaum, Sarah ; Ekunwe, Lynette ; Hirschhorn, Joel N ; Henderson, Brian E ; Myers, Simon ; Haiman, Christopher A ; Reich, David ; Patterson, Nick ; Wilson, James G ; Price, Alkes L Schork, Nicholas J.

PLoS genetics, 2011-04, Vol.7 (4), p.e1001371 [Periódico revisado por pares]

United States: Public Library of Science

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36
Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip
Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip
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Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

Spencer, Chris C A ; Su, Zhan ; Donnelly, Peter ; Marchini, Jonathan Storey, John D.

PLoS genetics, 2009-05, Vol.5 (5), p.e1000477-e1000477 [Periódico revisado por pares]

United States: Public Library of Science

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37
A knowledge-based weighting framework to boost the power of genome-wide association studies
A knowledge-based weighting framework to boost the power of genome-wide association studies
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A knowledge-based weighting framework to boost the power of genome-wide association studies

Li, Miao-Xin ; Sham, Pak C ; Cherny, Stacey S ; Song, You-Qiang Mailund, Thomas

PloS one, 2010-12, Vol.5 (12), p.e14480-e14480 [Periódico revisado por pares]

United States: Public Library of Science

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38
Mathematical analysis of copy number variation in a DNA sample using digital PCR on a nanofluidic device
Mathematical analysis of copy number variation in a DNA sample using digital PCR on a nanofluidic device
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Mathematical analysis of copy number variation in a DNA sample using digital PCR on a nanofluidic device

Dube, Simant ; Qin, Jian ; Ramakrishnan, Ramesh Wu, Xiaolin

PloS one, 2008-08, Vol.3 (8), p.e2876-e2876 [Periódico revisado por pares]

United States: Public Library of Science

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39
Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
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Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?

Casto, Amanda M ; Feldman, Marcus W Akey, Joshua M.

PLoS genetics, 2011-01, Vol.7 (1), p.e1001266-e1001266 [Periódico revisado por pares]

United States: Public Library of Science

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40
The impact of recombination on nucleotide substitutions in the human genome
The impact of recombination on nucleotide substitutions in the human genome
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The impact of recombination on nucleotide substitutions in the human genome

Duret, Laurent ; Arndt, Peter F Przeworski, Molly

PLoS genetics, 2008-05, Vol.4 (5), p.e1000071-e1000071 [Periódico revisado por pares]

United States: Public Library of Science

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