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Nucleic Acids Research
|
February 16, 2011
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm
Alberto Magi, Matteo Benelli, Seungtai Yoon, et al.
Genome Research
|
August 7, 2009
Sensitive and accurate detection of copy number variants using read depth of coverage
Seungtai Yoon, Zhenyu Xuan, Vladimir Makarov, et al.
BMC Genetics
|
February 3, 2006
A Bayesian approach for applying Haseman-Elston methods
Seungtai Yoon, Young Ju Suh, Nancy Role Mendell, et al.
Bioinformatics (Oxford, England)
|
January 20, 2012
AnnTools: a comprehensive and versatile annotation toolkit for genomic variants
Vladimir Makarov, Tina O'Grady, Guiqing Cai, et al.
G3 (Bethesda, Md.)
|
March 3, 2012
Inferring haplotypes of copy number variations from high-throughput data with uncertainty
Mamoru Kato, Seungtai Yoon, Naoya Hosono, et al.
American Journal of Human Genetics
|
December 6, 2011
Finding disease variants in Mendelian disorders by using sequence data: methods and applications
Iuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, et al.
BMC Proceedings
|
March 1, 2012
Principal components ancestry adjustment for Genetic Analysis Workshop 17 data
Jing Jin, Jane E Cerise, Sun Jung Kang, et al.
Cell Genomics
|
June 30, 2023
Sharing parental genomes by siblings concordant or discordant for autism
Mathew Wroten, Seungtai Yoon, Peter Andrews, et al.
BMC Proceedings
|
May 10, 2008
Mixture modeling of microarray gene expression data
Yang Yang, Adam P Tashman, Jung Yeon Lee, et al.
Human Genetics
|
September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia
Jose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Nucleic Acids Research
|
February 16, 2011
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm
Alberto Magi, Matteo Benelli, Seungtai Yoon, et al.
Genome Research
|
August 7, 2009
Sensitive and accurate detection of copy number variants using read depth of coverage
Seungtai Yoon, Zhenyu Xuan, Vladimir Makarov, et al.
BMC Genetics
|
February 3, 2006
A Bayesian approach for applying Haseman-Elston methods
Seungtai Yoon, Young Ju Suh, Nancy Role Mendell, et al.
Bioinformatics (Oxford, England)
|
January 20, 2012
AnnTools: a comprehensive and versatile annotation toolkit for genomic variants
Vladimir Makarov, Tina O'Grady, Guiqing Cai, et al.
G3 (Bethesda, Md.)
|
March 3, 2012
Inferring haplotypes of copy number variations from high-throughput data with uncertainty
Mamoru Kato, Seungtai Yoon, Naoya Hosono, et al.
American Journal of Human Genetics
|
December 6, 2011
Finding disease variants in Mendelian disorders by using sequence data: methods and applications
Iuliana Ionita-Laza, Vlad Makarov, Seungtai Yoon, et al.
BMC Proceedings
|
March 1, 2012
Principal components ancestry adjustment for Genetic Analysis Workshop 17 data
Jing Jin, Jane E Cerise, Sun Jung Kang, et al.
Cell Genomics
|
June 30, 2023
Sharing parental genomes by siblings concordant or discordant for autism
Mathew Wroten, Seungtai Yoon, Peter Andrews, et al.
BMC Proceedings
|
May 10, 2008
Mixture modeling of microarray gene expression data
Yang Yang, Adam P Tashman, Jung Yeon Lee, et al.
Human Genetics
|
September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia
Jose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Page
of 3