☆13Feb 10, 2021Updated 5 years ago
Alternatives and similar repositories for Strandscript
Users that are interested in Strandscript are comparing it to the libraries listed below
Sorting:
- A Rare Variant Caller for Array-based Genotyping☆25Feb 25, 2015Updated 11 years ago
- Script to convert GTC/BPM files to VCF☆48Oct 13, 2025Updated 4 months ago
- An R package for import, QC and analysis of Illumina Infinium genotyping arrays☆35Mar 20, 2018Updated 7 years ago
- Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF☆163Aug 20, 2025Updated 6 months ago
- Sanity check Variant Call Format (VCF) files.☆37Mar 18, 2016Updated 9 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- FELLA: an R package for Metabolomics data enrichment through diffusion☆23Jan 23, 2026Updated last month
- A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample☆26May 4, 2023Updated 2 years ago
- ADS1263 bare-metal driver for MCUs☆11May 17, 2018Updated 7 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 3 years ago
- We apply deep learning approaches to accurately identify 30 common bacterial pathogens, achieving an average isolate-level accuracy of ov…☆13Feb 27, 2021Updated 5 years ago
- Late nights, long commits, quiet focus. A colorscheme for performance.☆14Jan 18, 2026Updated last month
- A benchmark on predicting how small molecules change gene expression in different cell types.☆15Jul 4, 2025Updated 7 months ago
- Application for Raman Spectroscopy Analysis☆13Jan 24, 2025Updated last year
- Lipid identification software for discovery LC-MS/MS☆12Mar 29, 2019Updated 6 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- PaNeV: an R package for a pathway-based network visualization☆10Aug 25, 2025Updated 6 months ago
- ☆17Jan 17, 2026Updated last month
- Systematic Multi-Trait AAV Capsid Engineering for Efficient Gene Delivery (Eid et al., Nature Communications, 2024)☆11Aug 26, 2024Updated last year
- Alignment workflow for Kids-First DRC☆11Feb 12, 2026Updated 2 weeks ago
- K-RET: Knowledgeable Biomedical Relation Extraction System☆10Feb 22, 2025Updated last year
- 🌓 Allele specific analyses across cell states and conditions☆10Nov 28, 2022Updated 3 years ago
- LAAVA: Long-read AAV Analysis☆13Dec 9, 2025Updated 2 months ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Sep 3, 2019Updated 6 years ago
- Lazy TUI to handle chezmoi dotfiles☆13Feb 1, 2025Updated last year
- Retrieve and normalize records from ICTRP☆10May 26, 2020Updated 5 years ago
- ☆11Feb 4, 2026Updated 3 weeks ago
- an app for storing and calculating with arbitrary structures of values.☆11Dec 25, 2017Updated 8 years ago
- http://tinyurl.com/cruk-shiny☆11Sep 13, 2017Updated 8 years ago
- Generating Protein Variants with Different Generative Models (HMM, VAE, ESM-2, ProtGPT2)☆11Mar 14, 2024Updated last year
- Integrating Ribo-SEQ Upstream and Downstream Analysis☆11Oct 14, 2024Updated last year
- Motif Transformers for Predicting Protein-Protein Interactions Between a Novel Virus and Humans☆10Dec 4, 2024Updated last year
- WhatsGNU: a tool for identifying proteomic novelty☆14Jan 27, 2025Updated last year
- Bayesian-based fetal genotyping using maternal cell-free DNA and parental sequencing data.☆14Jun 5, 2019Updated 6 years ago
- NGS perl modules☆11Updated this week
- A beautiful, vibrant Neovim colorscheme inspired by spring blossoms with a soft, dreamy aesthetic.☆21Jan 5, 2026Updated last month
- Generic methods, types and modules for the BioJulia ecosystem.☆12Jul 11, 2024Updated last year
- Machine Learning based toxicity prediction tool for small molecules.☆11Feb 13, 2024Updated 2 years ago
- Pipeline to generate variant catalogues, a list of variants and their frequencies in a population, from whole genome sequences.☆13Jun 3, 2025Updated 8 months ago