A Transposon-Based Strategy for Sequencing Repetitive DNA in Eukaryotic Genomes

Por Devine, Scott E., Chissoe, Stephanie L., Eby, Yolanda, Wilson, Richard K., Boeke, Jef D.
Publicado em 1997

Representation of cloned genomic sequences in two sequencing vectors: correlation of DNA sequence and subclone distribution.

Por Chissoe, S L, Marra, M A, Hillier, L, Brinkman, R, Wilson, R K, Waterston, R H
Publicado em 1997

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 no BMC Bioinformatics (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 em 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 no Pharmacogenet Genomics (2017)

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe

Por Rubio, Justin P., Topp, Simon, Warren, Liling, St Jean, Pamela L., Wegmann, Daniel, Kessner, Darren, Novembre, John, Shen, Judong, Fraser, Dana, Aponte, Jennifer, Nangle, Keith, Cardon, Lon R., Ehm, Margaret G., Chissoe, Stephanie L., Whittaker, John C., Nelson, Matthew R., Mooser, Vincent E.
Publicado em 2012

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 em 2012

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

Por Nelson, Matthew R., Wegmann, Daniel, Ehm, Margaret G., Kessner, Darren, St. Jean, Pamela, Verzilli, Claudio, Shen, Judong, Tang, Zhengzheng, Bacanu, Silviu-Alin, Fraser, Dana, Warren, Liling, Aponte, Jennifer, Zawistowski, Matthew, Liu, Xiao, Zhang, Hao, Zhang, Yong, Li, Jun, Li, Yun, Li, Li, Woollard, Peter, Topp, Simon, Hall, Matthew D., Nangle, Keith, Wang, Jun, Abecasis, Gonçalo, Cardon, Lon R., Zöllner, Sebastian, Whittaker, John C., Chissoe, Stephanie L., Novembre, John, Mooser, Vincent
Publicado no Science (2012)

Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes

Por Ellsworth, Rachel E., Jamison, D. Curtis, Touchman, Jeffrey W., Chissoe, Stephanie L., Braden Maduro, Valerie V., Bouffard, Gerard G., Dietrich, Nicole L., Beckstrom-Sternberg, Stephen M., Iyer, Leslie M., Weintraub, Lauren A., Cotton, Marc, Courtney, Laura, Edwards, Jennifer, Maupin, Rachel, Ozersky, Philip, Rohlfing, Theresa, Wohldmann, Patricia, Miner, Tracie, Kemp, Kimberley, Kramer, Jason, Korf, Ian, Pepin, Kimberlie, Antonacci-Fulton, Lucinda, Fulton, Robert S., Minx, Patrick, Hillier, LaDeana W., Wilson, Richard K., Waterston, Robert H., Miller, Webb, Green, Eric D.
Publicado em 2000