Search "+saasCNV"

Positive matches

• 0.225 + - Allele-specific copy number profiling by next-generation DNA sequencing
• 0.143 + - 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
• 0.143 + - SNP array
• 0.143 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
• 0.143 + - Allele-specific copy number
• 0.143 + - WGS
• 0.143 + - CNV calling from NGS data
• 0.143 + - Exome sequencing
• 0.065 + - ngCGH
• 0.025 + - Copy-number variation
• 0.025 + - Genetics in Medicine
• 0.025 + - July 7
• 0.025 + - March 9
• 0.025 + - Sequence assembly
• 0.025 + - April 18
• 0.025 + - SNP
• 0.024 + - BMC Genetics
• 0.024 + - An evaluation of copy number variation detection tools from whole-exome sequencing data
• 0.024 + - NGS
• 0.024 + - November 3

Negative matches