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American Journal of Human Genetics
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January 17, 2017
Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits
Alanna C Morrison, Zhuoyi Huang, Bing Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 5, 2019
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
Desheng Liang, David S Cram, Hu Tan, et al.
Human Mutation
|
December 17, 2015
Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses
Ian M Campbell, Tomasz Gambin, Shalini Jhangiani, et al.
Science (New York, N.Y.)
|
April 21, 2007
Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens"
Fuli Yu, R Sean Hill, Stephen F Schaffner, et al.
BMC Genomics
|
April 19, 2015
PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations
Min Wang, Christine R Beck, Adam C English, et al.
Human Mutation
|
March 2, 2017
Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development
Yiyun Chen, Justin Bartanus, Desheng Liang, et al.
BMC Bioinformatics
|
January 31, 2014
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
Jeffrey G Reid, Andrew Carroll, Narayanan Veeraraghavan, et al.
Plos Genetics
|
October 6, 2005
Positive selection of a pre-expansion CAG repeat of the human SCA2 gene
Fuli Yu, Pardis C Sabeti, Paul Hardenbol, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2018
Rho Guanine Nucleotide Exchange Factor <i>ARHGEF17</i> Is a Risk Gene for Intracranial Aneurysms
Xinyu Yang, Jiani Li, Yabo Fang, et al.
American Journal of Obstetrics and Gynecology
|
June 1, 2018
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
Jing Wang, Lin Chen, Cong Zhou, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
American Journal of Human Genetics
|
January 17, 2017
Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits
Alanna C Morrison, Zhuoyi Huang, Bing Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 5, 2019
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
Desheng Liang, David S Cram, Hu Tan, et al.
Human Mutation
|
December 17, 2015
Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses
Ian M Campbell, Tomasz Gambin, Shalini Jhangiani, et al.
Science (New York, N.Y.)
|
April 21, 2007
Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens"
Fuli Yu, R Sean Hill, Stephen F Schaffner, et al.
BMC Genomics
|
April 19, 2015
PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations
Min Wang, Christine R Beck, Adam C English, et al.
Human Mutation
|
March 2, 2017
Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development
Yiyun Chen, Justin Bartanus, Desheng Liang, et al.
BMC Bioinformatics
|
January 31, 2014
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
Jeffrey G Reid, Andrew Carroll, Narayanan Veeraraghavan, et al.
Plos Genetics
|
October 6, 2005
Positive selection of a pre-expansion CAG repeat of the human SCA2 gene
Fuli Yu, Pardis C Sabeti, Paul Hardenbol, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2018
Rho Guanine Nucleotide Exchange Factor <i>ARHGEF17</i> Is a Risk Gene for Intracranial Aneurysms
Xinyu Yang, Jiani Li, Yabo Fang, et al.
American Journal of Obstetrics and Gynecology
|
June 1, 2018
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
Jing Wang, Lin Chen, Cong Zhou, et al.
Page
of 6