NCBI BLAST finds regions of similarity between biological sequences.
a suite of tools to address common questions raised in genomic studies.
Toolkit for processing sequences in FASTA/Q formats.
Reading/writing BCF2/VCF/gVCF files and calling/filtering/summarising SNP
Tools (written in C using htslib) for manipulating next-generation sequencing data
C library for high-throughput sequencing data formats
Bioinformatics Research and Achievement Display Platform for BIO SIG
Efficient phylogenomic software by maximum likelihood
A program for the Bayesian estimation of phylogeny
A tool for automated alignment trimming in large-scale phylogenetic analyses
Multiple alignment program for amino acid or nucleotide sequences
Tools for early stage alignment file processing
The Community repo is to store all the information about openEuler Community, inclouding governance, SIGs(project teams), Communications and etc.
C++ API & command-line toolkit for working with BAM data
Picard is a set of command line tools for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
libdeflate is a library for fast, whole-buffer DEFLATE-based compression and decompression, supporting DEFLATE, gzip, and zlib.
the bedtools utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks
