Interface between matplotlib and plotly
☆13Jun 26, 2014Updated 12 years ago
Alternatives and similar repositories for matplotlylib
Users that are interested in matplotlylib 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
- Creates a rarefaction curve to measure complexity in RNA Seq data using start position☆13Apr 2, 2017Updated 9 years ago
- Simple interval class for fast fasta access☆10Jun 18, 2012Updated 14 years ago
- Blacktie: a streamlined interface to the popular tophat/cufflinks RNA-seq pipeline☆26Oct 5, 2015Updated 11 years ago
- The original version of MGA has been archived - please see https://github.com/crukci-bioinformatics/mga2 instead.☆24Apr 15, 2021Updated 5 years ago
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- A python script used to annotate genomic intervals.☆18May 29, 2020Updated 6 years ago
- Fast and Accurate Classification of Sequences using Bloom filters☆16Apr 19, 2023Updated 3 years ago
- Playing around with the human genome and Clojure☆11Mar 15, 2022Updated 4 years ago
- Report generator for Chanjo output☆10Jun 5, 2024Updated 2 years ago
- Simple interface to BioMart (Python -> rpy2 -> R/BioConductor's biomaRt)☆15May 21, 2014Updated 12 years ago
- Analyze exome data for Mendelian disorders. Still in alpha-testing.☆10Apr 13, 2016Updated 10 years ago
- ☆17Sep 24, 2013Updated 13 years ago
- picking up low allelic-fraction, somatic variants from tumor samples☆14Jan 4, 2018Updated 8 years ago
- Railroadtracks is a Python package to handle connected computation steps for DNA and RNA Seq.☆14Jun 22, 2015Updated 11 years ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- eXtasy: Variant Prioritization by Genomic Data Fusion☆13Feb 19, 2014Updated 12 years ago
- Python package for managing sessions in the UCSC Genome Browser.☆11Mar 19, 2015Updated 11 years ago
- A Ruffus pipeline for Analysis of High-Throughput Sequencing data☆12Apr 3, 2013Updated 13 years ago
- Resources that facilitate and automate the analysis of RNA-Seq data☆12Aug 30, 2019Updated 7 years ago
- A tool to examine duplicate read characteristics in a BAM file☆12Dec 8, 2017Updated 8 years ago
- Directly create a bigwig file with signal derived from a sorted and indexed bam file.☆11Jul 7, 2017Updated 9 years ago
- Wrappers around NGS peak callers to both call peaks and run IDR☆11Aug 2, 2013Updated 13 years ago
- python wrapper to dpryan79's bigwig library using cffi☆18May 13, 2016Updated 10 years ago
- Genomics database manager☆25Mar 3, 2014Updated 12 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.
- Computational Framework to reconstructing tumor clone structures☆15Mar 31, 2021Updated 5 years ago
- Normalization and difference calling for Next Generation Sequencing (NGS) data via joint multinomial modeling.☆11May 21, 2026Updated 5 months ago
- Use somatic mutations to choose a personalized cancer vaccine (tumor-specific immunogenic peptides)☆16Sep 23, 2016Updated 10 years ago
- Basic, no assumptions, multi-pileup☆24Mar 26, 2014Updated 12 years ago
- Infrastructure code to support DNA pipeline☆38May 5, 2015Updated 11 years ago
- Concordance between variant callers☆17Nov 27, 2014Updated 11 years ago
- Contig Ploidy and Allele Dosage Estimation☆12Oct 30, 2015Updated 11 years ago
- example of shiny plots which react to clicking on points☆11Jun 18, 2015Updated 11 years ago
- A small library for ranges/intervals, for use with genomic data.☆17Nov 27, 2012Updated 13 years ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- A package for simulating RNA-seq library preparation with parameter estimation☆23Mar 3, 2014Updated 12 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Oct 2, 2026Updated last month
- fast bloomfilter☆21May 13, 2014Updated 12 years ago
- A tool for Read Multi-Mapper Resolution☆25Feb 15, 2017Updated 9 years ago
- Mostly deprecated in favor of : https://github.com/hbc/bcbioRNASeq. Quality control, differential gene/transcript expression and pathway …☆26Dec 11, 2017Updated 8 years ago
- hyb: a bioinformatics pipeline for the analysis of CLASH (crosslinking, ligation and sequencing of hybrids) data☆14Jul 12, 2024Updated 2 years ago
- Fast Structural Variation Detection Toolbox☆19Feb 16, 2015Updated 11 years ago
Are these results useful?