xapple / trackLinks
Provides easy read/write access to genomic tracks
☆22Updated 9 years ago
Alternatives and similar repositories for track
Users that are interested in track are comparing it to the libraries listed below
Sorting:
- Novel Adjacency Identification with Barcoded Reads☆13Updated 3 years ago
- A configurable de novo assembly pipeline☆28Updated 9 years ago
- Docker images of bioinformatics software☆21Updated 8 years ago
- gvcf aggregation tool☆12Updated 7 years ago
- An ultra fast and accurate paired-end adapter trimmer that needs no a priori adapter sequences.☆22Updated 5 years ago
- Stupid Simple Structural Variant View☆25Updated 9 years ago
- Hemang Parikh☆11Updated 10 years ago
- ☆36Updated 5 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆25Updated 9 years ago
- laSV is a software package that employs local assembly to detect structural variations from whole-genome high-throughput sequencing datas…☆12Updated 9 years ago
- Convert CWL to WDL☆17Updated 9 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated last year
- Wrapper for RTG's vcfeval; DEPRECATED!☆21Updated 9 years ago
- normalize, left-align, trim, validate and clean VCF files☆20Updated 10 years ago
- program for haplotype phasing from sequence reads and related tools☆25Updated 7 years ago
- Specific Transposable Element Aligner (HERV-K)☆16Updated 6 years ago
- Graph based multi genome aligner☆49Updated 4 years ago
- Generate and process BAM files from Illumina sequencing instrument files☆23Updated 9 years ago
- Tandem Repeat Annotation Library☆25Updated 2 years ago
- GenoTypes Compressor☆16Updated 3 years ago
- DNA assembler developed on FER (Croatia), RBI (Croatia) and GIS (Singapore)☆18Updated 10 years ago
- A tutorial for learning de novo assembly☆33Updated 14 years ago
- ☆16Updated 9 years ago
- FermiKit small variant calls for public SGDP samples☆17Updated 9 years ago
- create a gemini-compatible database from a VCF☆55Updated 5 years ago
- This repository contains information about ongoing analysis performed by GIAB☆14Updated 6 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated last week
- HGVS variant description extractor☆11Updated 5 years ago
- vcf file manipulation☆22Updated 10 years ago
- Variant caller GUI + genetic disease analysis☆22Updated 5 years ago