There are 4 repositories under fasta topic.
A cross-platform and ultrafast toolkit for FASTA/Q file manipulation
Renderers and renderer extensions for JupyterLab
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
a python package for fast random access to sequences from plain and gzipped FASTA/Q files
Clone with Python! Data structures for double stranded DNA & simulation of homologous recombination, Gibson assembly, cut & paste cloning.
A modern compressor for genomic files (FASTQ, SAM/BAM/CRAM, VCF, FASTA, GFF/GTF/GVF, 23andMe...), up to 5x better than gzip and faster too
Precision genomics for everyone, everywhere. Powered by private AI.
Redundans is a pipeline that assists an assembly of heterozygous/polymorphic genomes.
GET_HOMOLOGUES: a versatile software package for pan-genome analysis
Goalign is a set of command line tools and an API to manipulate multiple sequence alignments. It is implemented in Go language.
FluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Nucleotide Archival Format - Compressed file format for DNA/RNA/protein sequences
Fast FASTA/Q parser and writer (C++ re-implementation of kseq library)
pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)
Generate unique KMERs for every contig in a FASTA file
Prepares a SARS-CoV-2 submission for GISAID, NCBI or ENA. Can read GISAID or NCBI files, or plain fasta+tsv/csv/xls. Finds files in input directory and merges everything into a single output directory. Auto-detects input file formats. Can submit the results to multiple repositories from the command line.