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Human Mutation|February 24, 2015
Oncotator: cancer variant annotation toolAlex H Ramos, Lee Lichtenstein, Manaswi Gupta, et al.EMBO Molecular Medicine|March 8, 2017
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutationsRam Ajore, David Raiser, Marie McConkey, et al.Plos One|April 21, 2017
Somatic copy number alterations in gastric adenocarcinomas among Asian and Western patientsSteven E Schumacher, Byoung Yong Shim, Giovanni Corso, et al.Plos One|February 6, 2014
A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing eventsAngela N Brooks, Peter S Choi, Luc de Waal, et al.Cell Systems|March 30, 2018
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesKyle Ellrott, Matthew H Bailey, Gordon Saksena, et al.Bioinformatics (Oxford, England)|August 30, 2022
Tangent normalization for somatic copy-number inference in cancer genome analysisGalen F Gao, Coyin Oh, Gordon Saksena, et al.Nature Genetics|July 16, 2013
An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancersSteven A Roberts, Michael S Lawrence, Leszek J Klimczak, et al.Nature Genetics|September 28, 2013
Pan-cancer patterns of somatic copy number alterationTravis I Zack, Stephen E Schumacher, Scott L Carter, et al.Nature Communications|September 22, 2020
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.Nature Communications|December 1, 2020
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samplesMatthew H Bailey, William U Meyerson, Lewis Jonathan Dursi, et al.Pageof 4