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Bioinformatics (Oxford, England)
|
August 2, 2011
ContEst: estimating cross-contamination of human samples in next-generation sequencing data
Kristian Cibulskis, Aaron McKenna, Tim Fennell, et al.
Genome Research
|
July 21, 2010
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna, Matthew Hanna, Eric Banks, et al.
Nature Biotechnology
|
February 12, 2013
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
Kristian Cibulskis, Michael S Lawrence, Scott L Carter, et al.
Current Protocols in Human Genetics
|
June 29, 2010
Targeted exon sequencing by in-solution hybrid selection
Brendan Blumenstiel, Kristian Cibulskis, Sheila Fisher, et al.
The Journal of Clinical Investigation
|
July 17, 2012
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers
Ryan S Lee, Chip Stewart, Scott L Carter, et al.
Human Mutation
|
October 16, 2012
A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder
Erik G Puffenberger, Robert N Jinks, Heng Wang, et al.
Nature Biotechnology
|
May 1, 2012
Absolute quantification of somatic DNA alterations in human cancer
Scott L Carter, Kristian Cibulskis, Elena Helman, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Accelerating scRNA-seq Analysis: Automated cell type annotation using representation learning and vector search
Stephen R Williams, Fedor Grab, Govinda M Kamath, et al.
Nature Biotechnology
|
September 16, 2015
Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes
Sachet A Shukla, Michael S Rooney, Mohini Rajasagi, et al.
Blood
|
June 4, 2014
Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemia
Mohini Rajasagi, Sachet A Shukla, Edward F Fritsch, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 62) with videos related to
Sort By:
Page
of 7
Bioinformatics (Oxford, England)
|
August 2, 2011
ContEst: estimating cross-contamination of human samples in next-generation sequencing data
Kristian Cibulskis, Aaron McKenna, Tim Fennell, et al.
Genome Research
|
July 21, 2010
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna, Matthew Hanna, Eric Banks, et al.
Nature Biotechnology
|
February 12, 2013
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
Kristian Cibulskis, Michael S Lawrence, Scott L Carter, et al.
Current Protocols in Human Genetics
|
June 29, 2010
Targeted exon sequencing by in-solution hybrid selection
Brendan Blumenstiel, Kristian Cibulskis, Sheila Fisher, et al.
The Journal of Clinical Investigation
|
July 17, 2012
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers
Ryan S Lee, Chip Stewart, Scott L Carter, et al.
Human Mutation
|
October 16, 2012
A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder
Erik G Puffenberger, Robert N Jinks, Heng Wang, et al.
Nature Biotechnology
|
May 1, 2012
Absolute quantification of somatic DNA alterations in human cancer
Scott L Carter, Kristian Cibulskis, Elena Helman, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Accelerating scRNA-seq Analysis: Automated cell type annotation using representation learning and vector search
Stephen R Williams, Fedor Grab, Govinda M Kamath, et al.
Nature Biotechnology
|
September 16, 2015
Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes
Sachet A Shukla, Michael S Rooney, Mohini Rajasagi, et al.
Blood
|
June 4, 2014
Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemia
Mohini Rajasagi, Sachet A Shukla, Edward F Fritsch, et al.
Page
of 7