davidebolo1993 / VISORLinks
VarIant SimulatOR for short, long and linked reads
☆49Updated 9 months ago
Alternatives and similar repositories for VISOR
Users that are interested in VISOR are comparing it to the libraries listed below
Sorting:
- Structural variant caller for real-time long-read sequencing data☆57Updated 2 years ago
- SRF: Satellite Repeat Finder☆97Updated last year
- Tools for the analysis of structural variation in genomes☆80Updated last year
- Toolkit for calling structural variants using short or long reads☆107Updated last week
- PGR-TK: Pangenome Research Tool Kit☆100Updated last year
- Reference-based variant calling pipeline for a pair of phased haplotype assemblies☆101Updated 4 years ago
- ☆77Updated 5 years ago
- Collection of tools for the analysis of CpG data☆87Updated 3 weeks ago
- Application of pan-genome for population☆108Updated 9 months ago
- Show pangenome graphs in an easy way☆56Updated last week
- Methylation Phasing for Nanopore Sequencing☆48Updated 2 years ago
- A list of software for pangenomics☆121Updated last week
- Phased assembly variant caller☆123Updated 8 months ago
- Call select base modifications in PacBio HiFi reads☆10Updated 6 months ago
- Evaluate variant calls and its combination with k-mer multiplicity☆67Updated 2 years ago
- A program for assessing the T2T genome continuity☆83Updated last month
- Mapping pipeline for data generated using Arima-HiC☆79Updated last year
- A local-haplotagging-based small and structural variant caller☆78Updated last week
- Variant annotation and merging pipeline☆39Updated 2 weeks ago
- Copy number variant caller and depth visualization utility for PacBio HiFi reads☆43Updated 9 months ago
- Pipeline to convert a haploid assembly into diploid☆102Updated 6 months ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆122Updated last week
- Hybrid error correction of long reads using colored de Bruijn graphs☆102Updated 10 months ago
- Fast and accurate coordinate conversion between assemblies☆114Updated 4 months ago
- ☆63Updated last week
- ☆116Updated 3 months ago
- Copy number caller for long read data including SNV utilization☆65Updated 4 months ago
- A fast tool for detecting and decomposing segmental duplications in genome assemblies☆49Updated 2 weeks ago
- ☆134Updated 3 months ago
- Set of tools to manipulate and visualize modified base bam files☆56Updated 3 years ago