BoevaLab / SV-BayLinks
Detection of structural variants in cancer mate-pair and paired-end data
☆12Updated 6 years ago
Alternatives and similar repositories for SV-Bay
Users that are interested in SV-Bay are comparing it to the libraries listed below
Sorting:
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆23Updated 4 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Updated 5 years ago
- Structural variation and indel detection using rolling local string graph assembly☆9Updated 8 years ago
- Using reference-free compressed data structures to analyse thousands of human genomes (1000 Genomes ReadServer)☆14Updated 7 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆38Updated 2 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- Accurate, Lightweight Clustering of de novo Transcriptomes using Fragment Equivalence Classes☆31Updated 11 months ago
- A Framework to call Structural Variants from NGS based datasets☆22Updated 7 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 9 months ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants