An online database of variants functionally demonstrated to affect (or not affect) splicing.
☆11Apr 28, 2026Updated 3 weeks ago
Alternatives and similar repositories for SpliceVarDB
Users that are interested in SpliceVarDB are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Accessing AlphaMissense Data Resources in R☆13Nov 26, 2025Updated 5 months ago
- Software to process, statistically analyse and visualise deep mutational scanning data☆14Apr 28, 2026Updated 3 weeks ago
- Benchmarking variant calling in polyploids☆16Nov 26, 2021Updated 4 years ago
- Accompanying analysis code for the FRASER manuscript☆25Aug 27, 2020Updated 5 years ago
- ☆20Nov 17, 2025Updated 6 months 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.
- customizable robust Independent Component Analysis (ICA)☆12Sep 16, 2024Updated last year
- Rare Disease variant reanalysis tool☆34Updated this week
- nPoRe: n-Polymer Realigner for improved pileup-based variant calling☆18Jul 11, 2022Updated 3 years ago
- A deep learning-based SNP calling method to identify SNPs based on low-coverage Nanopore sequencing reads.☆21Nov 20, 2022Updated 3 years ago
- Python Client Library for the G2P Portal API☆15Aug 14, 2025Updated 9 months ago
- My animations for my videos☆12Jan 26, 2019Updated 7 years ago
- 🏃♀️🎨 R package for quick extraction of color palettes from text and images☆27Apr 29, 2021Updated 5 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Mar 10, 2018Updated 8 years ago
- FRASER - Find RAre Splicing Events in RNA-seq☆55Feb 11, 2026Updated 3 months 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.
- ☆50Sep 4, 2025Updated 8 months ago
- Pangolin is a deep-learning method for predicting splice site strengths.☆88Jun 17, 2024Updated last year
- Simulate patients with rare genetic conditions☆24Jul 28, 2023Updated 2 years ago
- Toolkit for calling and analyzing de novo STR mutations☆17Dec 17, 2023Updated 2 years ago
- Research Object BagIt archive☆21Jan 13, 2023Updated 3 years ago
- Python Matrix Factorization Module☆14Mar 13, 2017Updated 9 years ago
- Metadata indexer and query service used for AnVIL, HCA, LungMAP, and CGP☆11Updated this week
- An R htmlwidgets package of phylotree.js☆18Feb 26, 2015Updated 11 years ago
- ☆96Apr 3, 2026Updated last month
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Fully sync two secure-scuttlebutt databases over a duplex stream.☆15Jun 13, 2018Updated 7 years ago
- qstat wrapper☆17Nov 25, 2020Updated 5 years ago
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Nov 17, 2021Updated 4 years ago
- Repository☆10Oct 23, 2024Updated last year
- Pynocular is a lightweight ORM that lets you query your database using Pydantic models and asyncio☆11May 24, 2022Updated 4 years ago
- Infrastructure setup.☆10Jul 27, 2019Updated 6 years ago
- ☆20Jul 28, 2025Updated 9 months ago
- This is a Python script to generate Sunburst Charts that visualise the structure of English words.☆16Mar 6, 2019Updated 7 years ago
- Docker for Bioinformatics☆20Mar 27, 2026Updated last month
- 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.
- ☆10Dec 17, 2025Updated 5 months ago
- Prioritization of functional rare genetic variants by integrating genomic annotations and RNA-seq☆19Dec 6, 2022Updated 3 years ago
- Rapid and accurate ancestry inference using SNVs.☆28Aug 15, 2025Updated 9 months ago
- Implementation of multiple clustering algorithms (K-means, Bisecting K-means, Agglomerative Hierarchial Clustering with Intra-Cluster Sim…☆22Aug 25, 2013Updated 12 years ago
- Companion to "A genome-wide almanac of co-essential modules assigns function to uncharacterized genes" (https://doi.org/10.1101/827071)☆27Jul 19, 2022Updated 3 years ago
- Implicit matrix factorization as outlined in http://www2.research.att.com/~yifanhu/PUB/cf.pdf.☆18Sep 18, 2014Updated 11 years ago
- SIMD aligned data structures to work with `std::simd`.☆11Dec 14, 2024Updated last year