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Starred repositories
Architected for speed. Automated for easy. Monitoring and troubleshooting, transformed!
A versatile pairwise aligner for genomic and spliced nucleotide sequences
Tools (written in C using htslib) for manipulating next-generation sequencing data
Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
bedtools - the swiss army knife for genome arithmetic
C library for high-throughput sequencing data formats
De novo assembler for single molecule sequencing reads using repeat graphs
This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html
Official home of genome aligner based upon notion of Cactus graphs
Redbean: A fuzzy Bruijn graph approach to long noisy reads assembly
Fast and accurate de novo assembler for long reads
lumpy: a general probabilistic framework for structural variant discovery
Short read de novo assembler using de Bruijn graphs, as published in: D.R. Zerbino and E. Birney. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Research, 1…
Inference of ploidy and heterozygosity structure using whole genome sequencing data
UCSC Genome Browser source tree. Stable branch: "beta".
Tools for manipulating sequence graphs in the GFA and rGFA formats
software tools for haplotype assembly from sequence data
Fast and accurately polish the genome generated by long reads.
Wavefront alignment algorithm (WFA): Fast and exact gap-affine pairwise alignment