mviewMView extracts and reformats the results of a sequence database search or multiple alignment.
nafNucleotide Archival Format - Compressed file format for DNA/RNA/protein sequences
perfPERF is an Exhaustive Repeat Finder
polyA Go package for engineering organisms.
fucFrequently used commands in bioinformatics
FluentDNAFluentDNA 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.
freqgen🎯 Generate DNA sequences with specified amino acid, codon, and k-mer frequencies
angsd-wrapperUtilities for analyzing next generation sequencing data.
tidysqtidy processing of biological sequences in R
hts-pythonpythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)
PlasFlowSoftware for prediction of plasmid sequences in metagenomic assemblies
pydnaClone with Python! Data structures for double stranded DNA & simulation of homologous recombination, Gibson assembly, cut & paste cloning.
redundansRedundans is a pipeline that assists an assembly of heterozygous/polymorphic genomes.
PairfqSync paired-end FASTA/Q files and keep singleton reads
biomisc Rcommand line bioinformatic scripts written in R
cljamA DNA Sequence Alignment/Map (SAM) library for Clojure