An online database of variants functionally demonstrated to affect (or not affect) splicing.
☆14Sep 22, 2026Updated last month
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:
- PubMind is a large language model (LLM)-assisted framework for Publication Mutation and information Discovery, designed to extract varian…☆15Aug 24, 2026Updated 2 months ago
- MaveDB API☆19Updated this week
- Single cell isoform heterogeneity and differential alternative splicing analysis☆14Sep 14, 2025Updated last year
- Accessing AlphaMissense Data Resources in R☆13Sep 7, 2026Updated last month
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆63Jul 29, 2026Updated 3 months ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- ☆11May 15, 2025Updated last year
- Collapsed Haplotype Pattern Method for Linkage Analysis of Next-Generation Sequencing Data☆11Apr 12, 2023Updated 3 years ago
- ☆19Oct 16, 2026Updated 2 weeks ago
- Software to process, statistically analyse and visualise deep mutational scanning data☆14Aug 3, 2026Updated 3 months ago
- Oncogenicity Variant Interpreter for somatic variants☆16Sep 8, 2026Updated last month
- ☆109Apr 3, 2026Updated 6 months ago
- Allele frequency filter app☆15May 4, 2022Updated 4 years ago
- ☆42Jul 3, 2025Updated last year
- FRASER - Find RAre Splicing Events in RNA-seq☆58Oct 27, 2026Updated last week
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- Nanopore sequencing-based episignature detection☆19Jun 10, 2026Updated 4 months ago
- An R interface to the GTEx Portal API☆13Aug 19, 2025Updated last year
- ☆15Jan 16, 2018Updated 8 years ago
- A mutation rate model at the basepair resolution identifies the mutagenic effect of Polymerase III transcription☆16Mar 17, 2026Updated 7 months ago
- ☆25Jul 29, 2025Updated last year
- A neural network model to predict splice site usage and splicing-altering mutations☆17Jul 24, 2025Updated last year
- customizable robust Independent Component Analysis (ICA)☆12Sep 16, 2024Updated 2 years ago
- Benchmarking variant calling in polyploids☆16Nov 26, 2021Updated 4 years ago
- A deep learning-based SNP calling method to identify SNPs based on low-coverage Nanopore sequencing reads.☆22Nov 20, 2022Updated 3 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.
- Accompanying analysis code for the FRASER manuscript☆25Aug 27, 2020Updated 6 years ago
- ☆17Dec 21, 2022Updated 3 years ago
- nPoRe: n-Polymer Realigner for improved pileup-based variant calling☆19Jul 11, 2022Updated 4 years ago
- A variant caller for the GBA gene using WGS data☆23Jul 31, 2024Updated 2 years ago
- ☆33Dec 6, 2024Updated last year
- Noise-Cancelling Repeat Finder☆27Apr 2, 2026Updated 7 months ago
- Pre-mAsking Long reads for Mobile Element inseRtion☆10Feb 27, 2023Updated 3 years ago
- Research Object BagIt archive☆22Jan 13, 2023Updated 3 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆18Mar 10, 2018Updated 8 years ago
- 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.
- Variant sequence context analysis tool☆10Jul 5, 2024Updated 2 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆32Jul 3, 2026Updated 4 months ago
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆39Mar 25, 2026Updated 7 months ago
- PanGenome Graph Building with the first 100 assemblies from the 1000G ONT Sequencing Consortium☆14Apr 5, 2025Updated last year
- ☆10Nov 11, 2024Updated last year
- A tool for diagnosing SMA in exome, genome or targeted sequencing data☆14Jul 1, 2026Updated 4 months ago
- Infrastructure setup.☆10Jul 27, 2019Updated 7 years ago