R
Free software environment for statistical computing and graphics
Rapptainer
Application containers for linux (previously known as Singularity)
apptainerapptainer
apptainer-overriden-nixosbedops
Suite of tools for addressing questions arising in genomics studies
bedopsbedtools
Powerful toolset for genome arithmetic
bedtoolsfastp
Ultra-fast all-in-one FASTQ preprocessor
fastpgenmap
Ultra-fast computation of genome mappability
genmaphisat2
Graph based aligner
hisat2isa-l
Collection of optimised low-level functions targeting storage applications
isa-llast
Genomic sequence aligner
lastminia
Short read genome assembler
miniamosdepth
Fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
mosdepthoctopus
Bayesian haplotype-based mutation calling
octopus-callerpicard-tools
Tools for high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF
picard-toolspython3.12-bx-python
Tools for manipulating biological data, particularly multiple sequence alignments
python312Packages.bx-pythonpython3.12-cnvkit
Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data
python312Packages.cnvkitpython3.12-pyfaidx
Python classes for indexing, retrieval, and in-place modification of FASTA files using a samtools compatible index
python312Packages.pyfaidxpython3.12-python-lzo
Python bindings for the LZO data compression library
python312Packages.python-lzobx-python
Tools for manipulating biological data, particularly multiple sequence alignments
python313Packages.bx-pythoncnvkit
Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data
python313Packages.cnvkit