FRASER - Find RAre Splicing Events in RNA-seq
☆55Feb 11, 2026Updated 3 months ago
Alternatives and similar repositories for FRASER
Users that are interested in FRASER are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Detecting Aberrant Splicing Events from RNA-sequencing data☆16Dec 10, 2024Updated last year
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆166Mar 24, 2026Updated 2 months ago
- Accompanying analysis code for the FRASER manuscript☆25Aug 27, 2020Updated 5 years ago
- OUTRIDER: OUTlier in RNA-seq fInDER is an R-based framework to find aberrantly expressed genes in RNA-seq data☆56Feb 11, 2026Updated 3 months ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 7 years 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.
- A list of alternative splicing analysis resources☆50Mar 26, 2025Updated last year
- Tests Allelic Expression data for extreme imbalance w.r.t. population☆11Oct 8, 2021Updated 4 years ago
- A nextflow pipeline for calling exome CNVs☆14May 19, 2026Updated last week
- An online database of variants functionally demonstrated to affect (or not affect) splicing.☆11Apr 28, 2026Updated 3 weeks ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆37Jul 1, 2024Updated last year
- ☆13May 13, 2024Updated 2 years ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 6 months ago
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Jun 2, 2022Updated 3 years ago
- Structural variant (SV) analysis tools☆41Jul 1, 2024Updated last year
- 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.
- alternative splicing analysis pipeline☆20Apr 9, 2021Updated 5 years ago
- Tool for the detection and quantification of alternative splicing events from RNA-Seq data.☆113Apr 13, 2026Updated last month
- RNA-seq analysis pipeline for detection of gene-fusions☆174Updated this week
- rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis☆64Jun 3, 2025Updated 11 months ago
- Alternative polyadenylation detection from diverse data sources such as 3'-seq, long-read and short-reads.☆36Nov 8, 2023Updated 2 years ago
- Command-line tool for the visualization of splicing events across multiple samples☆141Jun 28, 2024Updated last year
- Automatised pipeline of ConsensuSV workflow.☆24Aug 23, 2023Updated 2 years ago
- A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient☆18Apr 1, 2026Updated last month
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 2 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.
- reference-free transcriptome assembly for short and long reads☆109Mar 13, 2026Updated 2 months ago
- Visualizing transcript structure and annotation using ggplot2☆168Aug 24, 2024Updated last year
- A tool for diagnosing SMA in exome, genome or targeted sequencing data☆13Updated this week
- A curated list of bioinformatics bench-marking papers and resources.☆15Nov 27, 2019Updated 6 years ago
- ☆11Jul 13, 2018Updated 7 years ago
- web-based analysis tool for rare disease genomics☆204May 18, 2026Updated last week
- ☆39Apr 25, 2023Updated 3 years ago
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆18Mar 10, 2022Updated 4 years ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated last year
- 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.
- ☆16Jan 10, 2022Updated 4 years ago
- genetic variant expressions, annotation, and filtering for great good.☆274May 12, 2026Updated 2 weeks ago
- Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact (Illumina) reads.☆32Sep 19, 2022Updated 3 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 4 years ago
- python plotly Circos from VCF☆42Jun 20, 2024Updated last year
- fastVEP: High-performance Variant Effect Predictor in Rust☆87May 9, 2026Updated 2 weeks ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Dec 6, 2023Updated 2 years ago