Process management library
☆18Aug 17, 2022Updated 4 years ago
Alternatives and similar repositories for psh
Users that are interested in psh are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- DEPRECATED Lightweight bioinformatics pipeline tools using iPython☆14Dec 11, 2015Updated 10 years ago
- Python package for managing sessions in the UCSC Genome Browser.☆11Mar 19, 2015Updated 11 years ago
- Simple interval class for fast fasta access☆10Jun 18, 2012Updated 14 years ago
- Wrappers around NGS peak callers to both call peaks and run IDR☆11Aug 2, 2013Updated 13 years ago
- Blacktie: a streamlined interface to the popular tophat/cufflinks RNA-seq pipeline☆26Oct 5, 2015Updated 11 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- A small library for ranges/intervals, for use with genomic data.☆17Nov 27, 2012Updated 13 years ago
- python stuff I use☆21Feb 16, 2026Updated 8 months ago
- normalize, left-align, trim, validate and clean VCF files☆20Jul 22, 2015Updated 11 years ago
- A python script used to annotate genomic intervals.☆18May 29, 2020Updated 6 years ago
- Fast Structural Variation Detection Toolbox☆19Feb 16, 2015Updated 11 years ago
- indel haplotype visualization on the command line from BAM files☆12Mar 12, 2014Updated 12 years ago
- ☆12Sep 10, 2026Updated last month
- A suite of javascript apps for visualizing sequencing data☆12Nov 18, 2013Updated 12 years ago
- Copy number estimation of highly duplicated sequences☆12Aug 15, 2017Updated 9 years ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- A support vector machine for calling variants from next-gen sequencing data☆15Dec 12, 2013Updated 12 years ago
- Basic, no assumptions, multi-pileup☆24Mar 26, 2014Updated 12 years ago
- collection of small scripts or how-tos that don't fall under a separate project☆20Oct 18, 2017Updated 9 years ago
- BigWig manpulation tools using libBigWig and htslib☆30Aug 8, 2024Updated 2 years ago
- laSV is a software package that employs local assembly to detect structural variations from whole-genome high-throughput sequencing datas…☆12Sep 26, 2016Updated 10 years ago
- This project is no longer maintained.☆13Oct 11, 2012Updated 14 years ago
- A Python QuickCheck implementation☆11Oct 18, 2018Updated 8 years ago
- ☆11Jan 10, 2018Updated 8 years ago
- franklin library for NGS sequencing analysis.☆25Oct 10, 2012Updated 14 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- VariantToolChest (VTC) is intended to be a powerful tool chest to analyze VCF files. I encourage anyone to contribute their tools and hel…☆25Apr 8, 2016Updated 10 years ago
- port of ruby's descriptive statistics to python☆15Feb 21, 2013Updated 13 years ago
- A Swiss army knife for genome projects☆15Aug 13, 2013Updated 13 years ago
- An extensible framework for genome assembly.☆12Nov 10, 2022Updated 3 years ago
- A configurable de novo assembly pipeline☆30Jun 29, 2016Updated 10 years ago
- Railroadtracks is a Python package to handle connected computation steps for DNA and RNA Seq.☆14Jun 22, 2015Updated 11 years ago
- A tool to identify, annotate and visualise splicing switch events from RNA-seq data☆14Aug 26, 2015Updated 11 years ago
- Computational Framework to reconstructing tumor clone structures☆15Mar 31, 2021Updated 5 years ago
- ☆17Sep 24, 2013Updated 13 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- ☆15Mar 7, 2016Updated 10 years ago
- Multiscale representation of genomic signals☆13Jan 31, 2017Updated 9 years ago
- Concordance between variant callers☆17Nov 27, 2014Updated 11 years ago
- The gkno launcher for executing tools or pipelines☆31Jan 17, 2017Updated 9 years ago
- Hotspot is a program for identifying genomic regions of local enrichment of short-read sequence tags.☆16Apr 12, 2014Updated 12 years ago
- fast bloomfilter☆21May 13, 2014Updated 12 years ago
- A workflow assembler for cancer genome analytics and informatics☆19Nov 16, 2016Updated 9 years ago