Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing
Jens G. Lohr(Dana-Farber Cancer Institute), Todd R. Golub(Broad Institute), Petar Stojanov(Broad Institute), Claudia Rangel‐Escareño(National Institute of Genomic Medicine), Birgit Knoechel(Broad Institute), Iván Imaz-Rosshandler(MRC Laboratory of Molecular Biology), Joshua Gould(Eli and Edythe Broad Foundation), Eric S. Lander(Broad Institute), Margaret A. Shipp(Broad Institute), Yan W. Asmann(Mayo Clinic in Florida), Ahmet Doǧan(Memorial Sloan Kettering Cancer Center), Thomas M. Habermann(Mayo Clinic in Arizona), Anne J. Novak(Mayo Clinic), Enrique Hernández–Lemus(National Institute of Genomic Medicine), Gordon Saksena, Daniel Auclair(Multiple Myeloma Research Foundation), Stephen M. Ansell(Mayo Clinic), Lihua Zou(Affiliated Hospital of Southwest Medical University), Peter Cruz‐Gordillo(Broad Institute), Susan L. Slager(Mayo Clinic), Nicolas Stransky(Broad Institute), Michael S. Lawrence(Broad Institute), Akinyemi I. Ojesina(Medical College of Wisconsin), Bjoern Chapuy(University of Göttingen), James R. Cerhan(Mayo Clinic), Juan Carlos Fernández-López(National Institute of Genomic Medicine), Carrie Sougnez(Broad Institute), Angela Schwarz‐Cruz y Celis(National Institute of Genomic Medicine), Brian K. Link(University of Iowa), Jorge Meléndez-Zajgla(National Institute of Genomic Medicine), Chandra Sekhar Pedamallu(Broad Institute), Gad Getz(Broad Institute), Joonil Jung(Broad Institute), Alfredo Hidalgo‐Miranda(National Institute of Genomic Medicine)
Cited by 990
Related Papers
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
|Proceedings of the National Academy of Sciences|2005|56.5k
Initial sequencing and analysis of the human genome
|Nature|2001|24.6k
A global reference for human genetic variation
|Nature|2015|20.3k
Integrative genomics viewer
|Nature Biotechnology|2011|16.5k