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Cancer Discovery|April 4, 2024
Somatic Mutations in Normal Tissues: Calm before the StormZahraa Rahal, Paul Scheet, Humam KadaraGenetic Epidemiology|August 17, 2016
A meta-analytic framework for detection of genetic interactionsYulun Liu, Yong Chen, Paul ScheetGenetic Epidemiology|December 20, 2018
System for Quality-Assured Data Analysis: Flexible, reproducible scientific workflowsJerry Fowler, Francis Anthony San Lucas, Paul ScheetGenome Research|December 8, 2011
Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate dispositionLaura B Ramsey, Gitte H Bruun, Wenjian Yang, et al.Genetic Epidemiology|January 22, 2011
A comparison of approaches to account for uncertainty in analysis of imputed genotypesJin Zheng, Yun Li, Gonçalo R Abecasis, et al.Genetic Epidemiology|December 8, 2011
Haploscope: a tool for the graphical display of haplotype structure in populationsF Anthony San Lucas, Noah A Rosenberg, Paul ScheetBioinformatics (Oxford, England)|November 22, 2018
Directional allelic imbalance profiling and visualization from multi-sample data with RECURYasminka A Jakubek, F Anthony San Lucas, Paul ScheetCancer Prevention Research (Philadelphia, Pa.)|March 24, 2016
Early Events in the Molecular Pathogenesis of Lung CancerHumam Kadara, Paul Scheet, Ignacio I Wistuba, et al.Breast Cancer Research and Treatment|May 20, 2014
Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence dataSvasti Haricharan, Matthew N Bainbridge, Paul Scheet, et al.Bioinformatics (Oxford, England)|December 6, 2011
Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant toolsF Anthony San Lucas, Gao Wang, Paul Scheet, et al.Pageof 14