Search "+VarScan"

Positive matches

• 0.115 + - SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data
• 0.068 + - Allele-specific copy number profiling by next-generation DNA sequencing
• 0.055 + - ASCAT
• 0.050 + - ngCGH
• 0.045 + - Samtools
• 0.045 + - Java
• 0.045 + - Illumina
• 0.045 + - Copy-number variation
• 0.045 + - SNV calling from NGS data
• 0.045 + - Perl
• 0.045 + - NGS
• 0.045 + - BAM
• 0.045 + - SOLiD
• 0.045 + - Comparison of custom capture for targeted next-generation DNA sequencing
• 0.045 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
• 0.045 + - 2011
• 0.045 + - April 28
• 0.045 + - Evaluation of somatic copy number estimation tools for whole-exome sequencing data
• 0.045 + - Hyungyong Kim
• 0.045 + - WGS

Negative matches