Python package for normalization of gene expression matrices.
☆10Nov 30, 2019Updated 6 years ago
Alternatives and similar repositories for PyGMNormalize
Users that are interested in PyGMNormalize are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Pathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform☆17Dec 12, 2022Updated 3 years ago
- ☆14Sep 2, 2026Updated 2 months ago
- fastq quality assessment and filtering tool☆17Dec 10, 2022Updated 3 years ago
- API for FAIRMD Lipids Databank (formerly NMRlipids Databank)☆14Updated this week
- fork from https://sourceforge.net/projects/xmsannotator/☆11Oct 30, 2022Updated 4 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.
- geoRge: a computational tool for stable isotope labelling detection in LC/MS-based untargeted metabolomics☆11Sep 17, 2021Updated 5 years ago
- ☆10Oct 28, 2026Updated last week
- Analyse molecular dynamics simulations of interfacial and confined systems.☆17Updated this week
- Info about NIH-IRP Single Cell Users Group events☆12Nov 21, 2023Updated 2 years ago
- SCOUP is a probabilistic model to analyze single-cell expression data during differentiation☆10Apr 20, 2017Updated 9 years ago
- A Universal Modeling Language for Metabolic Flux Analysis☆12Oct 8, 2026Updated 3 weeks ago
- ☆18Apr 10, 2015Updated 11 years ago
- Iteratively Adjusted Surrogate Variable Analysis☆10Aug 23, 2021Updated 5 years ago
- nmrXiv is currently developed as the FAIR, consensus-driven NMR data repository and computational platform. The ultimate goal is to accel…☆22Updated this week
- End-to-end encrypted email - Proton Mail • AdSpecial offer: 40% Off Yearly / 80% Off First Month. All Proton services are open source and independently audited for security.
- A python library for replica exchange transition interface sampling with infinite swaps☆17May 26, 2026Updated 5 months ago
- An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictog…☆13Oct 16, 2026Updated 3 weeks ago
- Python nd2 reader based on the ND2 SDK☆17Jan 28, 2022Updated 4 years ago
- A python package for the prediction of chemical shieldings of organic solids and beyond.☆23Sep 30, 2026Updated last month
- Python Programming for Biologists☆13Dec 3, 2025Updated 11 months ago
- ☆15Jun 17, 2026Updated 4 months ago
- Normalization methods for RNA-Seq expression data in Python.☆11Jan 7, 2015Updated 11 years ago
- ☆17Apr 27, 2022Updated 4 years ago
- Detection of structural variants in cancer mate-pair and paired-end data☆13May 3, 2019Updated 7 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.
- Single Cell RNA-seq UMI Filtering Facilitator☆10Oct 6, 2025Updated last year
- A label free quantification tool.☆20Jan 13, 2026Updated 9 months ago
- A project to develop the R Shiny applications.☆12May 13, 2019Updated 7 years ago
- ☆13Oct 16, 2017Updated 9 years ago
- Scripts related to building major-allele references for Bowtie and Bowtie 2☆13Jun 3, 2021Updated 5 years ago
- Let's benchmark quantum chemistry packages!☆23Nov 3, 2020Updated 6 years ago
- robust matching of small variant datasets using flexible scoring schemes☆12Mar 26, 2020Updated 6 years ago
- Gene expression viewer template☆12Aug 30, 2017Updated 9 years ago
- Sequential model-based optimization with a `scipy.optimize` interface☆25Jun 4, 2024Updated 2 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- Allele-Specific Quantification of Structural Variations in Cancer Genomes☆19Mar 5, 2019Updated 7 years ago
- RNA Fusion Detection and Quantification☆18Oct 31, 2018Updated 8 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 10 years ago
- assembles images in a grid☆33Jan 30, 2020Updated 6 years ago
- 用每个窗口的read数作为特征、胎儿浓度作为标签，训练神经网络模型；训练完成的神经网络模型可用于NIPT胎儿浓度的预测☆11Jun 10, 2022Updated 4 years ago
- Code and figures accompanying the paper, "Single-cell alternative splicing analysis with Expedition reveals splicing dynamics during neu…☆20Jun 28, 2017Updated 9 years ago
- Single cell RNA Seq data analysis with quantitative phenotypes☆13Nov 17, 2020Updated 5 years ago