lh3 / longdustLinks
Identify long STRs, VNTRs, satellite DNA and other low-complexity regions in a genome
☆74Updated 3 weeks ago
Alternatives and similar repositories for longdust
Users that are interested in longdust are comparing it to the libraries listed below
Sorting:
- A Nextflow workflow to generate lift over files for any pair of genomes☆68Updated 3 months ago
- Joint structural variant and copy number variant caller for HiFi sequencing data☆61Updated 2 weeks ago
- A local-haplotagging-based small and structural variant caller☆85Updated this week
- VACmap: a long-read aligner specifically designed for complex structural variation discovery☆36Updated 2 months ago
- Compute N50/NG50 and auN/auNG☆32Updated 2 years ago
- ☆45Updated 2 months ago
- A bioinformatics tool for viewing and calculating base modification frequencies from BAM files☆37Updated 3 weeks ago
- Correcting errors in noisy long reads using variation graphs☆51Updated 2 years ago
- ☆66Updated last month
- Kmer Analysis of Pileups for Genotyping☆32Updated this week
- ☆36Updated 2 months ago
- Easy genomic regions for short-read variant calling☆44Updated last month
- A battery of methylation tools for PacBio HiFi reads☆42Updated last month
- MarginPolish: Graph based assembly polishing☆46Updated 4 years ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆52Updated 7 months ago
- ☆28Updated 2 years ago
- Long-read splice alignment with high accuracy☆63Updated last year
- A snakemake pipeline to assembly, polishing, correction and quality check from Oxford nanopore reads.☆36Updated 6 months ago
- Efficient low-divergence mapping of long reads in minimizer space☆66Updated 2 years ago
- MethPhaser: methylation-based haplotype phasing of human genomes☆49Updated 7 months ago
- ☆18Updated last year
- hifiasm_meta - de novo metagenome assembler, based on hifiasm, a haplotype-resolved de novo assembler for PacBio Hifi reads.☆69Updated last week
- Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)☆45Updated last month
- In-depth characterization and annotation of differences between two sets of DNA sequences☆62Updated 5 years ago
- Dot: An interactive dot plot viewer for comparative genomics☆34Updated 2 years ago
- ☆66Updated last year
- Pan-Genomic Matching Statistics☆53Updated last year
- Error correction of ONT transcript reads☆58Updated 2 years ago
- Exact Tandem Repeat Finder (not a TRF replacement)☆50Updated 5 years ago
- TELR is a fast non-reference transposable element detector from long read sequencing data.☆34Updated 2 years ago