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Trends in Genetics : TIG
|
January 13, 2015
Accounting for uncertainty in DNA sequencing data
Jason A O'Rawe, Scott Ferson, Gholson J Lyon
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline
Laura T Jiménez-Barrón, Jason A O'Rawe, Yiyang Wu, et al.
Peerj
|
October 11, 2013
Integrating precision medicine in the study and clinical treatment of a severely mentally ill person
Jason A O'Rawe, Han Fang, Shawn Rynearson, et al.
Nature Methods
|
August 18, 2014
Accurate de novo and transmitted indel detection in exome-capture data using microassembly
Giuseppe Narzisi, Jason A O'Rawe, Ivan Iossifov, et al.
Genome Medicine
|
November 27, 2014
Reducing INDEL calling errors in whole genome and exome sequencing data
Han Fang, Yiyang Wu, Giuseppe Narzisi, et al.
Nature Protocols
|
November 18, 2016
Indel variant analysis of short-read sequencing data with Scalpel
Han Fang, Ewa A Bergmann, Kanika Arora, et al.
American Journal of Human Genetics
|
December 7, 2015
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations
Jason A O'Rawe, Yiyang Wu, Max J Dörfel, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Trends in Genetics : TIG
|
January 13, 2015
Accounting for uncertainty in DNA sequencing data
Jason A O'Rawe, Scott Ferson, Gholson J Lyon
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline
Laura T Jiménez-Barrón, Jason A O'Rawe, Yiyang Wu, et al.
Peerj
|
October 11, 2013
Integrating precision medicine in the study and clinical treatment of a severely mentally ill person
Jason A O'Rawe, Han Fang, Shawn Rynearson, et al.
Nature Methods
|
August 18, 2014
Accurate de novo and transmitted indel detection in exome-capture data using microassembly
Giuseppe Narzisi, Jason A O'Rawe, Ivan Iossifov, et al.
Genome Medicine
|
November 27, 2014
Reducing INDEL calling errors in whole genome and exome sequencing data
Han Fang, Yiyang Wu, Giuseppe Narzisi, et al.
Nature Protocols
|
November 18, 2016
Indel variant analysis of short-read sequencing data with Scalpel
Han Fang, Ewa A Bergmann, Kanika Arora, et al.
American Journal of Human Genetics
|
December 7, 2015
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations
Jason A O'Rawe, Yiyang Wu, Max J Dörfel, et al.
Page
of 1