Multi-nucleotide variants (MNVs) in gnomAD 2.1
☆14Oct 29, 2026Updated this week
Alternatives and similar repositories for gnomad_mnv
Users that are interested in gnomad_mnv are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Multi-nucleotide Variation Annotation Corrector☆11Dec 13, 2022Updated 3 years ago
- A comprehensive and intelligent clinical phasing tool☆15Dec 3, 2022Updated 3 years ago
- Utilities to detect and profile `het-kmers`☆12Aug 5, 2024Updated 2 years ago
- ☆11Jun 14, 2023Updated 3 years ago
- Analysis code for the TAP-seq manuscript.☆13Jun 25, 2021Updated 5 years 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.
- A lightweight, alignment-free utility for detecting repeat-containing reads in short-read WGS, WES and RNA-seq data.☆19Jan 16, 2026Updated 9 months ago
- Swift Accel-Amplicon primer trimming tool for fast alignment-based primer trimming☆11Apr 6, 2021Updated 5 years ago
- ☆23Sep 21, 2021Updated 5 years ago
- python module for querying the vicc knowledgebase integration datastore☆11Jul 6, 2023Updated 3 years ago
- GWAS and rare variants tests at high speed using regenie☆16Oct 14, 2026Updated 2 weeks ago
- Mean Alterations Using Discrete Expression☆14Updated this week
- Source code for MutPred2.0☆16Mar 27, 2025Updated last year
- Mutation rate analysis of autosomal loci☆15Jun 25, 2020Updated 6 years ago
- ☆11Mar 4, 2025Updated last year
- 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.
- Clinical Variant Annotation Pipeline☆10Apr 21, 2020Updated 6 years ago
- A tool to detect structural variant☆17Mar 27, 2023Updated 3 years ago
- Adaptive haplotype assembly for efficiently leveraging high coverage in long reads☆13Sep 4, 2018Updated 8 years ago
- 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
- ☆16Jul 9, 2026Updated 3 months ago
- Code associated with MIX-seq manuscript☆16Aug 26, 2020Updated 6 years ago
- A tool set to assess the quality of the per read phasing and reduce the errors.☆13Jun 25, 2020Updated 6 years ago
- INC-Seq: Accurate single molecule reads using nanopore sequencing☆16Sep 11, 2020Updated 6 years ago
- a tool for annotation of immunoglobulin genes in genome assemblies☆15Sep 22, 2025Updated last year
- 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.
- MicrOSAtellite Instability Classifier☆15Apr 27, 2026Updated 6 months ago
- A simple variant calling and annotation pipeline using BWA, GATK and ENSEMBL.☆14Nov 29, 2013Updated 12 years ago
- ☆15Oct 24, 2024Updated 2 years ago
- Human mitochondrial variants annotation using HmtVar.☆18Oct 16, 2023Updated 3 years ago
- End-guided RNA assembler☆15Dec 2, 2025Updated 11 months ago
- Long read to reference genome mapping tool☆13Mar 14, 2024Updated 2 years ago
- Local Agentic Model Deployment on AI Cluster☆17Aug 27, 2026Updated 2 months ago
- Concordance and contamination estimator for tumor–normal pairs☆60Oct 22, 2024Updated 2 years ago
- cnv-seq with custom bugfix☆10Mar 23, 2013Updated 13 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.
- Portable database of microhaplotype marker and allele frequency data☆13Oct 2, 2025Updated last year
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- ☆57Jan 11, 2023Updated 3 years ago
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 7 years ago
- SEASTAR - Systematic Evaluation of Alternative transcription STArt site in RNA☆14Jan 21, 2018Updated 8 years ago
- R Package for phasing of single cell Strand-seq data☆11Jan 14, 2025Updated last year
- Supporting code and materials for GATK gCNV publication☆12Jul 13, 2022Updated 4 years ago