VarScan
From MaRDI portal
Cited in
(44)- MATHT: a web server for comprehensive transcriptome data analysis
- Exome sequencing identifies predisposing and fusion gene in ganglioneuroma, ganglioneuroblastoma and neuroblastoma
- GATK
- miRBase
- Samtools
- FASTX
- Trimmomatic
- RSEM
- ReadDepth
- Bioinformatics for high throughput sequencing
- Error correction in methylation profiling from NGS bisulfite protocols
- BS Seeker
- BSMAP
- MATHT
- TopHat-Fusion
- miTarget
- FunCoup
- DNMAD
- SNVMix
- mrsFAST
- Wileup
- topGO
- ReQON
- MultiQC
- SomaticSniper
- Strelka
- eSNV-detect
- MapSplice
- HaploReg
- abSNP
- RNASeqReadSimulator
- GlfMultiples
- Sniper
- MethylCoder
- abSNP: RNA-Seq SNP calling in repetitive regions via abundance estimation
- Analysis of expression profile and gene variation via development of methods for next generation sequencing data
- SomaticSignatures
- HitWalker
- Jannovar
- SNVer
- HTQC
- BCFtools
- ExomeWalker
- Computational exome and genome analysis
This page was built for software: VarScan
