smarco / BiWFA-paperLinks
Bidirectional WFA (Paper)
☆48Updated last year
Alternatives and similar repositories for BiWFA-paper
Users that are interested in BiWFA-paper are comparing it to the libraries listed below
Sorting:
- C implementation of the Landau-Vishkin algorithm☆35Updated 3 years ago
- A reimplementation of the WaveFront Alignment algorithm at low memory☆50Updated last year
- vcfdist: Accurately benchmarking phased variant calls☆84Updated 2 months ago
- Efficient low-divergence mapping of long reads in minimizer space☆68Updated 2 years ago
- ☆67Updated last year
- Dashing 2 is a fast toolkit for k-mer and minimizer encoding, sketching, comparison, and indexing.☆68Updated last year
- MarginPolish: Graph based assembly polishing☆47Updated 5 years ago
- BWT construction and search☆121Updated last week
- Banded Striped DNA Sequence Alignment☆49Updated 2 years ago
- Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)☆46Updated 3 months ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆52Updated 9 months ago
- A C++ library and utilities for manipulating the Graphical Fragment Assembly format.☆55Updated 3 years ago
- Pan-Genomic Matching Statistics☆54Updated last year
- Tumour-only somatic mutation calling using long reads☆28Updated last year
- Fast and exact gap-affine partial order alignment☆56Updated 3 weeks ago
- ☆36Updated 9 months ago
- PBSIM2: a simulator for long read sequencers with a novel generative model of quality scores☆73Updated 2 years ago
- Scalable long read self-correction and assembly polishing with multiple sequence alignment☆53Updated last year
- A repository for generating strobemers and evalaution☆79Updated last year
- Pangenome graphs (review article on graph-based pangenomic methods)☆72Updated 5 years ago
- ⚡️ 🧬 Fulgor is a fast and space-efficient colored de Bruijn graph index.☆57Updated 2 weeks ago
- Sensitive and Fast Alignment Search Tool for Long Read sequencing Data.☆41Updated 6 years ago
- ☆35Updated 5 years ago
- URMAP ultra-fast read mapper☆38Updated 5 years ago
- SAPLING: Suffix Array Piecewise Linear INdex for Genomics☆25Updated 5 years ago
- Symmetric DUST for finding low-complexity regions in DNA sequences☆45Updated 4 months ago
- Estimating k-mer coverage histogram of genomics data☆76Updated last year
- Gfapy: a flexible and extensible software library for handling sequence graphs in Python☆70Updated 3 weeks ago
- Optimized sequence graph implementations for graph genomics☆34Updated last week
- Joint structural variant and copy number variant caller for HiFi sequencing data☆65Updated last month