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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 4, 2013
Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data
Hao Hu, Chad D Huff
Proceedings of the National Academy of Sciences of the United States of America
|
November 16, 2017
Reply to Mafessoni and Prüfer: Inferences with and without singleton site patterns
Alan R Rogers, Ryan J Bohlender, Chad D Huff
BMC Genomics
|
January 7, 2010
Detecting positive selection from genome scans of linkage disequilibrium
Chad D Huff, Henry C Harpending, Alan R Rogers
Proceedings of the National Academy of Sciences of the United States of America
|
August 9, 2017
Early history of Neanderthals and Denisovans
Alan R Rogers, Ryan J Bohlender, Chad D Huff
Genome Medicine
|
August 27, 2016
VARPRISM: incorporating variant prioritization in tests of de novo mutation association
Hao Hu, Hilary Coon, Man Li, et al.
Plos One
|
October 27, 2015
The Relationship between Native American Ancestry, Body Mass Index and Diabetes Risk among Mexican-Americans
Hao Hu, Chad D Huff, Yuko Yamamura, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2010
Mobile elements reveal small population size in the ancient ancestors of Homo sapiens
Chad D Huff, Jinchuan Xing, Alan R Rogers, et al.
Molecular Biology and Evolution
|
February 3, 2007
Ancestral alleles and population origins: inferences depend on mutation rate
Alan R Rogers, Stephen Wooding, Chad D Huff, et al.
Genetic Epidemiology
|
July 10, 2013
VAAST 2.0: improved variant classification and disease-gene identification using a conservation-controlled amino acid substitution matrix
Hao Hu, Chad D Huff, Barry Moore, et al.
Journal of Medical Genetics
|
May 25, 2020
Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma
Fulan Hu, Yao Yu, Jiun-Sheng Chen, et al.
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of 9
Search research articles
Search
Showing results (1-10 of 88) with videos related to
Sort By:
Page
of 9
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 4, 2013
Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data
Hao Hu, Chad D Huff
Proceedings of the National Academy of Sciences of the United States of America
|
November 16, 2017
Reply to Mafessoni and Prüfer: Inferences with and without singleton site patterns
Alan R Rogers, Ryan J Bohlender, Chad D Huff
BMC Genomics
|
January 7, 2010
Detecting positive selection from genome scans of linkage disequilibrium
Chad D Huff, Henry C Harpending, Alan R Rogers
Proceedings of the National Academy of Sciences of the United States of America
|
August 9, 2017
Early history of Neanderthals and Denisovans
Alan R Rogers, Ryan J Bohlender, Chad D Huff
Genome Medicine
|
August 27, 2016
VARPRISM: incorporating variant prioritization in tests of de novo mutation association
Hao Hu, Hilary Coon, Man Li, et al.
Plos One
|
October 27, 2015
The Relationship between Native American Ancestry, Body Mass Index and Diabetes Risk among Mexican-Americans
Hao Hu, Chad D Huff, Yuko Yamamura, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 6, 2010
Mobile elements reveal small population size in the ancient ancestors of Homo sapiens
Chad D Huff, Jinchuan Xing, Alan R Rogers, et al.
Molecular Biology and Evolution
|
February 3, 2007
Ancestral alleles and population origins: inferences depend on mutation rate
Alan R Rogers, Stephen Wooding, Chad D Huff, et al.
Genetic Epidemiology
|
July 10, 2013
VAAST 2.0: improved variant classification and disease-gene identification using a conservation-controlled amino acid substitution matrix
Hao Hu, Chad D Huff, Barry Moore, et al.
Journal of Medical Genetics
|
May 25, 2020
Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma
Fulan Hu, Yao Yu, Jiun-Sheng Chen, et al.
Page
of 9