☆21Aug 30, 2022Updated 4 years ago
Alternatives and similar repositories for MLVar
Users that are interested in MLVar are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- REEV: Explanation and Evaluation of Variants☆11Apr 27, 2026Updated 6 months ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated last year
- Automatic classification of sequence variants and CNVs according to ACMG criteria.☆34Sep 30, 2024Updated 2 years ago
- ☆13Dec 7, 2021Updated 4 years ago
- ☆17Oct 17, 2024Updated 2 years ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- Clinical machine-learning based interpreter of germline mutations.☆11Mar 13, 2025Updated last year
- ☆12Sep 30, 2026Updated last month
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10May 7, 2017Updated 9 years ago
- Clinical Variant Annotation Pipeline☆10Apr 21, 2020Updated 6 years ago
- iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Genera…☆16Jun 11, 2026Updated 4 months ago
- KIV2/D4Z4 genotyper using HiFi WGS data☆18Aug 9, 2026Updated 2 months ago
- A nextflow pipeline for calling CNVs in probe-enriched sequencing workflows☆14Oct 20, 2026Updated 2 weeks ago
- Prioritize structural variants based on CADD scores☆29May 7, 2020Updated 6 years ago
- Detect somatic variants from tumor and normal WGS/WXS data☆21Sep 21, 2026Updated last month
- 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.
- ☆19Mar 14, 2022Updated 4 years ago
- A tool for visualizing alignments of reads in regions containing tandem repeats☆92Apr 20, 2026Updated 6 months ago
- A tool to detect postzygotic single-nucleotide mosaicism from unpaired, trio, or paired samples.☆13Feb 23, 2021Updated 5 years ago
- Structural variant pipeline☆18Jun 25, 2020Updated 6 years ago
- Ancestry and haplotype aware simulation of genotypes and phenotypes for complex trait analysis☆28Updated this week
- Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores …☆17Aug 9, 2018Updated 8 years ago
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆27Jun 22, 2026Updated 4 months ago
- ☆25Jul 29, 2025Updated last year
- a tool for predicting mitochondrial DNA deletions using soft-clipping☆23Feb 3, 2022Updated 4 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.
- A Data Fusion Method for Multi Source (VCF4.0+) Structural Variation Analysis☆24Feb 4, 2025Updated last year
- Research pipeline for exploring clinically relevant genomic variants☆18Jul 20, 2026Updated 3 months ago
- Learn how to analyse NGS data using the latest bioinformatics tools and resources☆11Jul 5, 2024Updated 2 years ago
- ☆11Aug 29, 2022Updated 4 years ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 9 years ago
- WGS Pipeline☆13Jan 19, 2018Updated 8 years ago
- Phenotype driven gene prioritization for HPO☆53Jul 26, 2021Updated 5 years ago
- Tests Allelic Expression data for extreme imbalance w.r.t. population☆11Oct 8, 2021Updated 5 years ago
- PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.☆19Dec 28, 2022Updated 3 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- Bitscopic Interpreting ACMG Standards 2015☆37Oct 27, 2026Updated last week
- My coursework files for the classes that I took at Istanbul Technical University over the semesters☆13Aug 5, 2025Updated last year
- This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially …☆28May 28, 2026Updated 5 months ago
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Jun 2, 2022Updated 4 years ago
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Dec 13, 2019Updated 6 years ago
- Curated list of resources for variant prioritization☆16Nov 18, 2025Updated 11 months ago
- A local database infrastructure for analysis of targeted- and whole genome re-sequencing projects☆11Apr 7, 2015Updated 11 years ago