ndierckx / NOVOLociLinks
Haplotype-aware assembly of complex regions and small genomes
☆15Updated last month
Alternatives and similar repositories for NOVOLoci
Users that are interested in NOVOLoci are comparing it to the libraries listed below
Sorting:
- Hierarchical clustering of cgMLST☆11Updated last year
- convert a blast output to a bed file☆12Updated 10 years ago
- Yet another Hi-C scaffolding tool☆22Updated last year
- Cantù Lab @ UC Davis - Annotation pipeline - EVM based☆14Updated last year
- Improved Phased Assembler☆28Updated 3 years ago
- Command line tool to plot genomic coverage from a BAM file☆14Updated 2 years ago
- Nanopanel2: a somatic variant caller for Nanopore panel sequencing data☆11Updated 4 years ago
- plot genome alignment synteny☆21Updated 5 years ago
- Quality control plotting for long reads☆10Updated last year
- A nextflow pipeline for polishing CLR assemblies☆18Updated 2 years ago
- Scaffolding with Ultralong Reads☆15Updated 4 years ago
- Scripts for identifying sites with differential error rates in mapped nanopore DRS data☆11Updated 4 years ago
- Identification of segmental duplications in the genome☆27Updated 3 years ago
- A method for measuring chromosome-specific telomere length from long reads☆22Updated last year
- ☆28Updated last year
- Gap2Seq is a gap filling and insertion genotyping tool.☆22Updated last year
- ☆11Updated 3 years ago
- interactive Multi Objective K-mer Analysis☆23Updated 2 years ago
- Scripts to reproduce TrioBinning manuscript☆17Updated 5 years ago
- Simple pipeline to go from an alignment to a neutral model, using the PHAST toolkit☆11Updated 5 years ago
- An R package to infer and analyze synteny networks from protein sequences☆34Updated 3 months ago
- Simple script to generate whole-genome coverage plots☆19Updated 10 years ago
- A module for improving the insertion sequences of structural variant calls☆32Updated 4 years ago
- Human pan-genome analysis pipeline☆31Updated 5 years ago
- ☆18Updated last year
- ASTRAL for PaRalogs and Orthologs☆21Updated 3 years ago
- ☆16Updated 4 years ago
- ☆15Updated 3 years ago
- Tandem Repeats Finder: a program to analyze DNA sequences☆17Updated 3 months ago
- Correcting errors in noisy long reads using variation graphs☆50Updated 2 years ago