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Nature Communications
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March 21, 2024
Allele-specific transcriptional effects of subclonal copy number alterations enable genotype-phenotype mapping in cancer cells
Hongyu Shi, Marc J Williams, Gryte Satas, et al.
Bioinformatics (Oxford, England)
|
July 2, 2003
GeneComber: combining outputs of gene prediction programs for improved results
Sohrab P Shah, Graham P McVicker, Alan K Mackworth, et al.
Plos Computational Biology
|
February 23, 2019
Integrated structural variation and point mutation signatures in cancer genomes using correlated topic models
Tyler Funnell, Allen W Zhang, Diljot Grewal, et al.
BMC Bioinformatics
|
February 23, 2005
Atlas - a data warehouse for integrative bioinformatics
Sohrab P Shah, Yong Huang, Tao Xu, et al.
Bioinformatics (Oxford, England)
|
July 29, 2006
Integrating copy number polymorphisms into array CGH analysis using a robust HMM
Sohrab P Shah, Xiang Xuan, Ron J DeLeeuw, et al.
Nature Methods
|
January 10, 2017
Scalable whole-genome single-cell library preparation without preamplification
Hans Zahn, Adi Steif, Emma Laks, et al.
Genome Biology
|
April 24, 2015
Cis-regulatory somatic mutations and gene-expression alteration in B-cell lymphomas
Anthony Mathelier, Calvin Lefebvre, Allen W Zhang, et al.
Nature Methods
|
May 31, 2017
E-scape: interactive visualization of single-cell phylogenetics and cancer evolution
Maia A Smith, Cydney B Nielsen, Fong Chun Chan, et al.
Blood
|
March 27, 2010
Genome-wide copy number analysis of Hodgkin Reed-Sternberg cells identifies recurrent imbalances with correlations to treatment outcome
Christian Steidl, Adele Telenius, Sohrab P Shah, et al.
Nature Communications
|
October 1, 2024
Inferring replication timing and proliferation dynamics from single-cell DNA sequencing data
Adam C Weiner, Marc J Williams, Hongyu Shi, et al.
Page
of 15
Search research articles
Search
Showing results (11-20 of 150) with videos related to
Sort By:
Page
of 15
Nature Communications
|
March 21, 2024
Allele-specific transcriptional effects of subclonal copy number alterations enable genotype-phenotype mapping in cancer cells
Hongyu Shi, Marc J Williams, Gryte Satas, et al.
Bioinformatics (Oxford, England)
|
July 2, 2003
GeneComber: combining outputs of gene prediction programs for improved results
Sohrab P Shah, Graham P McVicker, Alan K Mackworth, et al.
Plos Computational Biology
|
February 23, 2019
Integrated structural variation and point mutation signatures in cancer genomes using correlated topic models
Tyler Funnell, Allen W Zhang, Diljot Grewal, et al.
BMC Bioinformatics
|
February 23, 2005
Atlas - a data warehouse for integrative bioinformatics
Sohrab P Shah, Yong Huang, Tao Xu, et al.
Bioinformatics (Oxford, England)
|
July 29, 2006
Integrating copy number polymorphisms into array CGH analysis using a robust HMM
Sohrab P Shah, Xiang Xuan, Ron J DeLeeuw, et al.
Nature Methods
|
January 10, 2017
Scalable whole-genome single-cell library preparation without preamplification
Hans Zahn, Adi Steif, Emma Laks, et al.
Genome Biology
|
April 24, 2015
Cis-regulatory somatic mutations and gene-expression alteration in B-cell lymphomas
Anthony Mathelier, Calvin Lefebvre, Allen W Zhang, et al.
Nature Methods
|
May 31, 2017
E-scape: interactive visualization of single-cell phylogenetics and cancer evolution
Maia A Smith, Cydney B Nielsen, Fong Chun Chan, et al.
Blood
|
March 27, 2010
Genome-wide copy number analysis of Hodgkin Reed-Sternberg cells identifies recurrent imbalances with correlations to treatment outcome
Christian Steidl, Adele Telenius, Sohrab P Shah, et al.
Nature Communications
|
October 1, 2024
Inferring replication timing and proliferation dynamics from single-cell DNA sequencing data
Adam C Weiner, Marc J Williams, Hongyu Shi, et al.
Page
of 15