Search "+ngCGH"

Positive matches

• 0.250 + - Python
• 0.250 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
• 0.250 + - CNV calling from NGS data
• 0.250 + - Comparative genomic hybridization
• 0.182 + - Allele-specific copy number profiling by next-generation DNA sequencing
• 0.087 + - Evaluation of somatic copy number estimation tools for whole-exome sequencing data
• 0.066 + - CNVkit
• 0.025 + - CoNIFER
• 0.025 + - Neoplasm
• 0.025 + - Programming language
• 0.025 + - January 23
• 0.025 + - 2013
• 0.024 + - An evaluation of copy number variation detection tools from whole-exome sequencing data
• 0.024 + - Copy-number variation
• 0.024 + - saasCNV
• 0.024 + - 2015
• 0.024 + - bioRxiv
• 0.024 + - Oncotarget
• 0.023 + - September 13
• 0.023 + - VarScan

Negative matches