ericminikel / minimal_representationLinks
Convert genetic variants to minimal representation
☆23Updated 7 years ago
Alternatives and similar repositories for minimal_representation
Users that are interested in minimal_representation are comparing it to the libraries listed below
Sorting:
- Keep Me Around: Intron Retention Detection☆29Updated 6 years ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆49Updated 6 years ago
- (DEPRECATED) epic: diffuse domain ChIP-Seq caller based on SICER☆31Updated 6 years ago
- Analysis from kallisto paper☆32Updated 9 years ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- Exon-exon splice junctions across SRA☆42Updated 4 years ago
- Haplotype, isoform and gene level expression analysis using multi-mapping RNA-seq reads☆68Updated last year
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 5 years ago