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

Positive matches

• 0.085 + - Gene expression
• 0.055 + - SNP array
• 0.050 + - DNA methylation
• 0.050 + - 2016
• 0.040 + - hppRNA-a Snakemake-based handy parameter-free pipeline for RNA-Seq analysis of numerous samples
• 0.040 + - Epigenetics in Human Disease
• 0.025 + - NGS
• 0.025 + - Scientific Reports
• 0.025 + - Cancer genomics
• 0.025 + - May 9
• 0.025 + - 2015
• 0.025 + - WIFA-Seq
• 0.022 + - Enhancer
• 0.019 + - GTEx
• 0.017 + - Landscape of somatic mutations in 560 breast cancer whole-genome sequences
• 0.014 + - CanineHD Whole-Genome Genotyping BeadChip
• 0.012 + - CNVkit
• 0.012 + - edgeR
• 0.011 + - GISTIC
• 0.011 + - saasCNV

Negative matches

• 0.160 + - Non-coding RNA
• 0.020 + - Hidden Markov model
• 0.020 + - Perl
• 0.020 + - Genome Research
• 0.020 + - 2007
• 0.020 + - October 5
• 0.020 + - BeadStudio
• 0.012 + - Genome-Wide Human SNP Array 6.0
• 0.012 + - Affymetrix Power Tools
• 0.008 + - Comparison of custom capture for targeted next-generation DNA sequencing
• 0.008 + - ASreml
• 0.006 + - 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
• 0.005 + - October 25
• 0.005 + - SNP
• 0.005 + - Dog
• 0.004 + - Markov process
• 0.004 + - CNV calling from NGS data
• 0.004 + - August 15
• 0.004 + - Markov model
• 0.003 + - Genetic variation