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Human Molecular Genetics
|
September 17, 2010
Analysis of next-generation genomic data in cancer: accomplishments and challenges
Li Ding, Michael C Wendl, Daniel C Koboldt, et al.
Nature Reviews. Genetics
|
July 9, 2014
Expanding the computational toolbox for mining cancer genomes
Li Ding, Michael C Wendl, Joshua F McMichael, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 10, 2021
AeQTL: eQTL analysis using region-based aggregation of rare genomic variants
Guanlan Dong, Michael C Wendl, Bin Zhang, et al.
Nature Cancer
|
February 5, 2022
Moving pan-cancer studies from basic research toward the clinic
Feng Chen, Michael C Wendl, Matthew A Wyczalkowski, et al.
Bioinformatics (Oxford, England)
|
April 19, 2011
PathScan: a tool for discerning mutational significance in groups of putative cancer genes
Michael C Wendl, John W Wallis, Ling Lin, et al.
Genome Research
|
April 10, 2007
PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data
Ken Chen, Michael D McLellan, Li Ding, et al.
Bioinformatics (Oxford, England)
|
December 28, 2013
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data
Beifang Niu, Kai Ye, Qunyuan Zhang, et al.
Genome Biology
|
August 15, 2015
Codon usage patterns in Nematoda: analysis based on over 25 million codons in thirty-two species
Makedonka Mitreva, Michael C Wendl, John Martin, et al.
Bioinformatics (Oxford, England)
|
June 6, 2017
BreakPoint Surveyor: a pipeline for structural variant visualization
Matthew A Wyczalkowski, Kristine M Wylie, Song Cao, et al.
Briefings in Bioinformatics
|
January 18, 2021
MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data
Xinyin Han, Shuying Zhang, Daniel Cui Zhou, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 95) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
September 17, 2010
Analysis of next-generation genomic data in cancer: accomplishments and challenges
Li Ding, Michael C Wendl, Daniel C Koboldt, et al.
Nature Reviews. Genetics
|
July 9, 2014
Expanding the computational toolbox for mining cancer genomes
Li Ding, Michael C Wendl, Joshua F McMichael, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
March 10, 2021
AeQTL: eQTL analysis using region-based aggregation of rare genomic variants
Guanlan Dong, Michael C Wendl, Bin Zhang, et al.
Nature Cancer
|
February 5, 2022
Moving pan-cancer studies from basic research toward the clinic
Feng Chen, Michael C Wendl, Matthew A Wyczalkowski, et al.
Bioinformatics (Oxford, England)
|
April 19, 2011
PathScan: a tool for discerning mutational significance in groups of putative cancer genes
Michael C Wendl, John W Wallis, Ling Lin, et al.
Genome Research
|
April 10, 2007
PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data
Ken Chen, Michael D McLellan, Li Ding, et al.
Bioinformatics (Oxford, England)
|
December 28, 2013
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data
Beifang Niu, Kai Ye, Qunyuan Zhang, et al.
Genome Biology
|
August 15, 2015
Codon usage patterns in Nematoda: analysis based on over 25 million codons in thirty-two species
Makedonka Mitreva, Michael C Wendl, John Martin, et al.
Bioinformatics (Oxford, England)
|
June 6, 2017
BreakPoint Surveyor: a pipeline for structural variant visualization
Matthew A Wyczalkowski, Kristine M Wylie, Song Cao, et al.
Briefings in Bioinformatics
|
January 18, 2021
MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data
Xinyin Han, Shuying Zhang, Daniel Cui Zhou, et al.
Page
of 10