Search "+WGS"

Positive matches

• 0.098 + - Comparative genomic hybridization
• 0.095 + - Allele-specific copy number
• 0.086 + - 잃어버린 유전 가능성(Missing heritability)에 대해
• 0.069 + - Pathology
• 0.061 + - VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
• 0.058 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
• 0.049 + - Cell-free tumor DNA
• 0.036 + - ExAC
• 0.036 + - AscatNgs
• 0.036 + - VarScan
• 0.036 + - 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
• 0.036 + - 암 맞춤의학과 생물정보학
• 0.036 + - Bipolar disorder
• 0.036 + - Copy-number variation
• 0.036 + - Genome
• 0.036 + - NGS
• 0.036 + - Breast cancer
• 0.036 + - Nanopore sequencing
• 0.036 + - gnomeAD
• 0.036 + - Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Negative matches