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Genetic Epidemiology
|
December 8, 2011
Haploscope: a tool for the graphical display of haplotype structure in populations
F Anthony San Lucas, Noah A Rosenberg, Paul Scheet
Bioinformatics (Oxford, England)
|
November 22, 2018
Directional allelic imbalance profiling and visualization from multi-sample data with RECUR
Yasminka A Jakubek, F Anthony San Lucas, Paul Scheet
Cancer Prevention Research (Philadelphia, Pa.)
|
March 24, 2016
Early Events in the Molecular Pathogenesis of Lung Cancer
Humam 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 data
Svasti 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 tools
F Anthony San Lucas, Gao Wang, Paul Scheet, et al.
JAMA Oncology
|
October 28, 2021
Evaluation of COVID-19 Mortality and Adverse Outcomes in US Patients With or Without Cancer
Mariana Chavez-MacGregor, Xiudong Lei, Hui Zhao, et al.
Genetic Epidemiology
|
November 9, 2010
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
Yun Li, Cristen J Willer, Jun Ding, et al.
Nature Genetics
|
February 24, 2006
Automating sequence-based detection and genotyping of SNPs from diploid samples
Matthew Stephens, James S Sloan, P D Robertson, et al.
Bioinformatics (Oxford, England)
|
June 12, 2016
Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq
F Anthony San Lucas, Smruthy Sivakumar, Selina Vattathil, et al.
Molecular Cancer Therapeutics
|
October 29, 2014
Cancer in silico drug discovery: a systems biology tool for identifying candidate drugs to target specific molecular tumor subtypes
F Anthony San Lucas, Jerry Fowler, Kyle Chang, et al.
Page
of 13
Search research articles
Search
Showing results (11-20 of 129) with videos related to
Sort By:
Page
of 13
Genetic Epidemiology
|
December 8, 2011
Haploscope: a tool for the graphical display of haplotype structure in populations
F Anthony San Lucas, Noah A Rosenberg, Paul Scheet
Bioinformatics (Oxford, England)
|
November 22, 2018
Directional allelic imbalance profiling and visualization from multi-sample data with RECUR
Yasminka A Jakubek, F Anthony San Lucas, Paul Scheet
Cancer Prevention Research (Philadelphia, Pa.)
|
March 24, 2016
Early Events in the Molecular Pathogenesis of Lung Cancer
Humam 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 data
Svasti 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 tools
F Anthony San Lucas, Gao Wang, Paul Scheet, et al.
JAMA Oncology
|
October 28, 2021
Evaluation of COVID-19 Mortality and Adverse Outcomes in US Patients With or Without Cancer
Mariana Chavez-MacGregor, Xiudong Lei, Hui Zhao, et al.
Genetic Epidemiology
|
November 9, 2010
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
Yun Li, Cristen J Willer, Jun Ding, et al.
Nature Genetics
|
February 24, 2006
Automating sequence-based detection and genotyping of SNPs from diploid samples
Matthew Stephens, James S Sloan, P D Robertson, et al.
Bioinformatics (Oxford, England)
|
June 12, 2016
Rapid and powerful detection of subtle allelic imbalance from exome sequencing data with hapLOHseq
F Anthony San Lucas, Smruthy Sivakumar, Selina Vattathil, et al.
Molecular Cancer Therapeutics
|
October 29, 2014
Cancer in silico drug discovery: a systems biology tool for identifying candidate drugs to target specific molecular tumor subtypes
F Anthony San Lucas, Jerry Fowler, Kyle Chang, et al.
Page
of 13