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Nature Biotechnology
|
May 12, 2010
Advancing RNA-Seq analysis
Brian J Haas, Michael C Zody
Genome Research
|
March 29, 2018
taxMaps: comprehensive and highly accurate taxonomic classification of short-read data in reasonable time
André Corvelo, Wayne E Clarke, Nicolas Robine, et al.
Nature Genetics
|
July 4, 2012
Structural haplotypes and recent evolution of the human 17q21.31 region
Linda M Boettger, Robert E Handsaker, Michael C Zody, et al.
Bioinformatics (Oxford, England)
|
November 9, 2002
Identification of mixups among DNA sequencing plates
Nikola Stojanovic, Jean L Chang, Jessica Lehoczky, et al.
BMC Genomics
|
October 4, 2013
V-Phaser 2: variant inference for viral populations
Xiao Yang, Patrick Charlebois, Alex Macalalad, et al.
Bioinformatics (Oxford, England)
|
June 30, 2016
Conpair: concordance and contamination estimator for matched tumor-normal pairs
Ewa A Bergmann, Bo-Juen Chen, Kanika Arora, et al.
Bioinformatics (Oxford, England)
|
May 30, 2009
Identifying novel constrained elements by exploiting biased substitution patterns
Manuel Garber, Mitchell Guttman, Michele Clamp, et al.
Genome Research
|
September 6, 2005
Why do human diversity levels vary at a megabase scale?
Ines Hellmann, Kay Prüfer, Hongkai Ji, et al.
Bioinformatics (Oxford, England)
|
November 26, 2020
Somatic variant analysis of linked-reads sequencing data with Lancet
Rajeeva Musunuri, Kanika Arora, André Corvelo, et al.
Nucleic Acids Research
|
June 11, 2013
ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
Chang Liu, Xiao Yang, Brian Duffy, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 108) with videos related to
Sort By:
Page
of 11
Nature Biotechnology
|
May 12, 2010
Advancing RNA-Seq analysis
Brian J Haas, Michael C Zody
Genome Research
|
March 29, 2018
taxMaps: comprehensive and highly accurate taxonomic classification of short-read data in reasonable time
André Corvelo, Wayne E Clarke, Nicolas Robine, et al.
Nature Genetics
|
July 4, 2012
Structural haplotypes and recent evolution of the human 17q21.31 region
Linda M Boettger, Robert E Handsaker, Michael C Zody, et al.
Bioinformatics (Oxford, England)
|
November 9, 2002
Identification of mixups among DNA sequencing plates
Nikola Stojanovic, Jean L Chang, Jessica Lehoczky, et al.
BMC Genomics
|
October 4, 2013
V-Phaser 2: variant inference for viral populations
Xiao Yang, Patrick Charlebois, Alex Macalalad, et al.
Bioinformatics (Oxford, England)
|
June 30, 2016
Conpair: concordance and contamination estimator for matched tumor-normal pairs
Ewa A Bergmann, Bo-Juen Chen, Kanika Arora, et al.
Bioinformatics (Oxford, England)
|
May 30, 2009
Identifying novel constrained elements by exploiting biased substitution patterns
Manuel Garber, Mitchell Guttman, Michele Clamp, et al.
Genome Research
|
September 6, 2005
Why do human diversity levels vary at a megabase scale?
Ines Hellmann, Kay Prüfer, Hongkai Ji, et al.
Bioinformatics (Oxford, England)
|
November 26, 2020
Somatic variant analysis of linked-reads sequencing data with Lancet
Rajeeva Musunuri, Kanika Arora, André Corvelo, et al.
Nucleic Acids Research
|
June 11, 2013
ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
Chang Liu, Xiao Yang, Brian Duffy, et al.
Page
of 11