Comparing variant calling algorithms for target-exon sequencing in a large sample

por Lo, Yancy, Kang, Hyun M, Nelson, Matthew R, Othman, Mohammad I, Chissoe, Stephanie L, Ehm, Margaret G, Abecasis, Gonçalo R, Zöllner, Sebastian
Publicado 2015

Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes

por Li, Li, Li, Yun, Browning, Sharon R., Browning, Brian L., Slater, Andrew J., Kong, Xiangyang, Aponte, Jennifer L., Mooser, Vincent E., Chissoe, Stephanie L., Whittaker, John C., Nelson, Matthew R., Ehm, Margaret Gelder
Publicado 2011

Characterization of ADME gene variation in 21 populations by exome sequencing

por Hovelson, Daniel H., Xue, Zhengyu, Zawistowski, Matthew, Ehm, Margaret G., Harris, Elizabeth C., Stocker, Sophie L., Gross, Annette S., Jang, In-Jin, Ieiri, Ichiro, Lee, Jong-Eun, Cardon, Lon R., Chissoe, Stephanie L., Abecasis, Gonçalo, Nelson, Matthew R.
Publicado 2017

Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

por Warren, Liling L., Li, Li, Nelson, Matthew R., Ehm, Margaret G., Shen, Judong, Fraser, Dana J., Aponte, Jennifer L., Nangle, Keith L., Slater, Andrew J., Woollard, Peter M., Hall, Matt D., Topp, Simon D., Yuan, Xin, Cardon, Lon R., Chissoe, Stephanie L., Mooser, Vincent, Morris, Andrew D., Palmer, Colin N.A., Perry, John R., Frayling, Timothy M., Whittaker, John C., Waterworth, Dawn M.
Publicado 2012