DKMS / Hapl-o-MatLinks
A software for haplotype inference
☆13Updated 8 months ago
Alternatives and similar repositories for Hapl-o-Mat
Users that are interested in Hapl-o-Mat are comparing it to the libraries listed below
Sorting:
- heuristics to merge structural variant calls in VCF format.☆38Updated 9 years ago
- ☆12Updated last year
- Computes various SV statistics☆14Updated 2 years ago
- Pipeline for structural variation detection in cohorts☆52Updated 4 years ago
- Fast and scalable variant annotation tool☆30Updated 3 years ago
- ☆84Updated 11 months ago
- This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially …☆27Updated 6 months ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- ☆51Updated 6 years ago
- CN-Learn☆30Updated 6 years ago
- Structural variant caller☆55Updated 4 years ago
- ☆19Updated this week
- UCSC Nanopore☆44Updated 6 years ago
- Enabling differential allele-specific analysis☆11Updated last year
- Automated human exome/genome variants detection from FASTQ files☆23Updated 4 years ago
- A simple script to create a customizable html file from an AnnotSV output.☆19Updated last year
- ☆35Updated 4 years ago
- Variant annotation and merging pipeline☆42Updated 6 months ago
- A tutorial on structural variant calling for short read sequencing data☆39Updated last year
- Whole Genome Sequenceing Structural Variation Pipelines☆18Updated 6 years ago
- Structural variant merging tool☆57Updated last year
- a tool for predicting mitochondrial DNA deletions using soft-clipping☆23Updated 4 years ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Updated 2 years ago
- Detection and genotyping of structural variants☆19Updated 3 months ago
- Population-wide Deletion Calling☆35Updated 9 months ago
- Tools to process LIANTI sequence data☆23Updated 6 years ago
- Copy number estimation and variant calling for duplicated genes using WGS.☆32Updated last week
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Updated 2 months ago
- new repo☆28Updated 4 years ago
- Code for phasing SVs with SNPs☆53Updated 5 years ago