Search "+WGS"

Positive matches

• 0.199 + - BRCA2
• 0.084 + - Allele-specific copy number
• 0.046 + - Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
• 0.045 + - Comparative genomic hybridization
• 0.045 + - Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
• 0.043 + - 잃어버린 유전 가능성(Missing heritability)에 대해
• 0.040 + - Liver cancer
• 0.038 + - HMEC
• 0.037 + - AscatNgs
• 0.037 + - VarScan
• 0.037 + - 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
• 0.037 + - 암 맞춤의학과 생물정보학
• 0.037 + - Bipolar disorder
• 0.037 + - Copy-number variation
• 0.037 + - NGS
• 0.037 + - Breast cancer
• 0.037 + - Nanopore sequencing
• 0.037 + - gnomeAD
• 0.037 + - Landscape of somatic mutations in 560 breast cancer whole-genome sequences
• 0.037 + - saasCNV

Negative matches