Ngs Python Packages

pysam

Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.

peppy

Project metadata manager for PEPs in Python

galaxy-tool-util

Data intensive science for everyone.

galaxy-util

Data intensive science for everyone.

galaxy-tool-util-models

Data intensive science for everyone.

deeptools

Tools to process and analyze deep sequencing data.

cooler

A cool place to store your Hi-C

pairtools

Extract 3D contacts (.pairs) from sequencing alignments

oxbow

Oxbow makes genomic data ready for high-performance analytics.

barcode

NGS barcode design and validation.

galaxy-objectstore

Data intensive science for everyone.

strkit

A short tandem repeat (STR) genotyping and analysis toolkit for long reads

sequana

Sequana: a set of Snakemake NGS pipelines

galaxy-job-metrics

Data intensive science for everyone.

galaxy-files

Data intensive science for everyone.

galaxy-data

Data intensive science for everyone.

galaxy-job-execution

Data intensive science for everyone.

galaxy-web-framework

Data intensive science for everyone.

galaxy-web-stack

Data intensive science for everyone.

galaxy-tours

Galaxy tours backend framework

galaxy-app

Galaxy application (backend)

wasp2

WASP2: High-performance allele-specific analysis pipeline for next-generation sequencing data

galaxy-auth

Galaxy auth framework and implementations

galaxy-containers

Data intensive science for everyone.