WGLab / LongReadSumLinks
☆24Updated this week
Alternatives and similar repositories for LongReadSum
Users that are interested in LongReadSum are comparing it to the libraries listed below
Sorting:
- Set of tools to manipulate and visualize modified base bam files☆56Updated 3 years ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- A Nextflow workflow to generate lift over files for any pair of genomes☆68Updated 3 months ago
- MethPhaser: methylation-based haplotype phasing of human genomes☆49Updated 6 months ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆50Updated 6 months ago
- Joint structural variant and copy number variant caller for HiFi sequencing data☆60Updated last week
- Error correction of ONT transcript reads☆58Updated 2 years ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆37Updated last year
- python plotly Circos from VCF☆39Updated last year
- A battery of methylation tools for PacBio HiFi reads☆41Updated last week
- Methylation Phasing for Nanopore Sequencing☆48Updated 2 years ago
- Structural variant merging tool☆54Updated last year
- WDL workflows for variant calling and assembly using ONT☆36Updated last week
- A local-haplotagging-based small and structural variant caller☆80Updated 2 weeks ago
- Method for inferring path posterior probabilities and abundances from pangenome graph read alignments