Search "+Long non-coding RNA -tRNA +Biochip +Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data -Cancer genomics"

Positive matches

• 0.090 + - Gene expression
• 0.075 + - SNP array
• 0.050 + - DNA methylation
• 0.047 + - 2016
• 0.040 + - hppRNA-a Snakemake-based handy parameter-free pipeline for RNA-Seq analysis of numerous samples
• 0.040 + - Epigenetics in Human Disease
• 0.034 + - Comparative genomic hybridization
• 0.025 + - Scientific Reports
• 0.025 + - Copy-number variation
• 0.025 + - WIFA-Seq
• 0.025 + - May 9
• 0.022 + - Enhancer
• 0.022 + - 2015
• 0.022 + - NGS
• 0.016 + - GISTIC
• 0.016 + - GTEx
• 0.014 + - Cattle
• 0.014 + - CanineHD Whole-Genome Genotyping BeadChip
• 0.014 + - Landscape of somatic mutations in 560 breast cancer whole-genome sequences
• 0.012 + - CNVkit

Negative matches

• 0.160 + - Non-coding RNA
• 0.029 + - Companion diagnostic
• 0.017 + - GDISC
• 0.016 + - Colorectal cancer
• 0.013 + - Ovarian cancer
• 0.011 + - Identification of druggable cancer driver genes amplified across TCGA datasets
• 0.010 + - Cloud computing
• 0.008 + - Glioblastoma
• 0.008 + - Peter Park
• 0.008 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
• 0.005 + - Pathology
• 0.005 + - Identification of Biomarkers for Breast Cancer Using Databases
• 0.005 + - 자연주의
• 0.005 + - Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
• 0.005 + - CODEX: a normalization and copy number variation detection method for whole exome sequencing
• 0.004 + - BRIC
• 0.004 + - 게놈
• 0.004 + - Human genome
• 0.003 + - VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
• 0.003 + - dbGaP