Generic Interactive Variant Analysis browser
☆29Apr 12, 2022Updated 4 years ago
Alternatives and similar repositories for iva
Users that are interested in iva are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- An Open Computational Genomics Analysis platform for big data genomics analysis. OpenCGA is maintained and develop by its parent company …☆179May 22, 2026Updated 3 weeks ago
- JSorolla is a JavaScript Library for biological and genomic data visualization. Found a bug or have an idea for a new feature? Let us kno…☆41Mar 12, 2026Updated 3 months ago
- High-Performance NoSQL database and RESTful web services to access to most relevant biological data. Found a bug or have an idea for a ne…☆95Mar 12, 2026Updated 3 months ago
- Website to analyze conflicting assertions in ClinVar☆19Mar 16, 2026Updated 2 months ago
- Java library that models biological entities and their equivalents in different file formats typically used in bioinformatics. Found a bu…☆30Mar 5, 2026Updated 3 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.
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- This repository implements converters and tools for working with NGS data in HPC or Hadoop cluster☆17Apr 13, 2018Updated 8 years ago
- gnomAD browser pre-ASHG 2018☆33Nov 2, 2020Updated 5 years ago
- Rapid and accurate ancestry inference using SNVs.☆28Aug 15, 2025Updated 9 months ago
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50May 8, 2026Updated last month
- Gene Exploration System for Variance☆22Dec 8, 2022Updated 3 years ago
- web-based analysis tool for rare disease genomics☆207Updated this week
- ☆21Oct 24, 2020Updated 5 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.
- Python API and React frontend for the Phenopolis Genomics Browser☆31Mar 12, 2026Updated 3 months ago
- This has been archived and active development transferred to gitlab.com/genomicsengland/gelreportmodels/GelReportModels☆14May 14, 2021Updated 5 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆32Jul 6, 2022Updated 3 years ago
- Convolutional Embedded Networks for Population Scale Clustering and Bio-ancestry Inferencing☆11Jan 7, 2020Updated 6 years ago
- A tool to extract LOH blocks from VCF, BAM and FASTA data☆25Aug 30, 2024Updated last year
- using all the bits for echt rapid variant annotation and filtering☆162Apr 30, 2026Updated last month
- Python client for GA4GH htsget protocol☆15Nov 7, 2022Updated 3 years ago
- SEQSpark documentation☆18Nov 17, 2020Updated 5 years ago
- CRyPTIC data processing pipelines☆35Jul 18, 2024Updated last year
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- LOVD3 development repository☆25Oct 13, 2025Updated 7 months ago
- Phylogeny-based Contamination Detection in Mitochondrial and Whole-Genome Sequencing Studies☆17Jun 14, 2023Updated 2 years ago
- Visualization and charting JS library for streaming genomic data☆19Dec 4, 2024Updated last year
- Gigabase: Synthetic Biology Cell Modeling Project☆19Nov 3, 2013Updated 12 years ago
- PopSTR - A Population based microsatellite genotyper☆32Oct 23, 2023Updated 2 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Feb 16, 2018Updated 8 years ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆43Nov 21, 2022Updated 3 years ago
- A Snakemake workflow to process single samples or cohorts of Illumina paired-end sequencing data (WGS or WES) using trim galore/bwa/GATK4…☆34Jan 13, 2023Updated 3 years ago
- COMPSRA: a COMprehensive Platform for Small RNA-Seq data Analysis☆17Jan 4, 2021Updated 5 years ago
- Open source password manager - Proton Pass • AdSecurely store, share, and autofill your credentials with Proton Pass, the end-to-end encrypted password manager trusted by millions.
- Tool to upload SARS-CoV-2 sequences to BH20 Arvados instance and orchestrate analysis☆13Sep 21, 2022Updated 3 years ago
- genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF☆150Feb 17, 2026Updated 3 months ago
- Cube Schema☆14May 17, 2026Updated 3 weeks ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 8 years ago
- ☆13Jun 4, 2026Updated last week
- A python3 package for operations on pedigree and genotype data☆21Nov 13, 2017Updated 8 years ago
- Repository for development of the genomic module of the CDM.☆26Jun 14, 2019Updated 6 years ago