Search "+An evaluation of copy number variation detection tools from whole-exome sequencing data"

Positive matches

• 0.102 + - ngCGH
• 0.101 + - Allele-specific copy number profiling by next-generation DNA sequencing
• 0.077 + - ExomeDepth
• 0.077 + - Hidden Markov model
• 0.077 + - Human Mutation
• 0.077 + - CoNIFER
• 0.077 + - PCA
• 0.077 + - XHMM]: [[PCA
• 0.077 + - XHMM
• 0.077 + - CONTRA
• 0.077 + - 2014
• 0.077 + - CNV calling from NGS data
• 0.077 + - Singular value decomposition
• 0.077 + - Exome sequencing
• 0.077 + - March 5
• 0.063 + - 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
• 0.062 + - CODEX
• 0.049 + - CNVkit
• 0.028 + - ASCAT
• 0.025 + - PyCon Korea 2014

Negative matches