scripts to automatically update ANNOVAR db
☆19Nov 17, 2021Updated 4 years ago
Alternatives and similar repositories for update_annovar_db
Users that are interested in update_annovar_db are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- The Exome Coverage and Identification Report displays the coverage of every target region in your capture design. It also displays regio…☆14Apr 22, 2015Updated 11 years ago
- 肿瘤突变负荷学习笔记(tumor mutation burden)☆17Dec 10, 2019Updated 6 years ago
- Microsatellite Analysis for Normal-Tumor InStability☆79Jul 14, 2022Updated 4 years ago
- WebApp for DNA variants interpretation☆16Updated this week
- automatic update Clinvar db for ANNOVAR☆11Updated this week
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Mutation Identification Pipeline. Read the latest documentation:☆47Nov 18, 2025Updated 9 months ago
- do some exercise☆15Dec 2, 2025Updated 9 months ago
- LOVD3 development repository☆26Jun 26, 2026Updated 2 months ago
- Haplotype-based somatic genome simulator☆10Apr 20, 2026Updated 4 months ago
- microsatellite instability detection using tumor only or paired tumor-normal data☆134Jan 6, 2021Updated 5 years ago
- This is a read-only mirror of the CRAN R package repository. sequenza — Copy Number Estimation from Tumor Genome Sequencing Data. Homep…☆22May 9, 2019Updated 7 years ago
- ☆10Jul 13, 2022Updated 4 years ago
- Microsatellite instability (MSI) detection for tumor only data.☆117Apr 23, 2024Updated 2 years ago
- ☆13Dec 7, 2021Updated 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.
- RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection☆29Oct 1, 2020Updated 5 years ago
- Annotates variants in MAF with OncoKB annotation.☆147Aug 25, 2026Updated last week
- Splicing Prediction Pipeline☆15Aug 12, 2023Updated 3 years ago
- Exome Copy Number Variation Polisher via Deep Learning☆18Jun 1, 2020Updated 6 years ago
- ☆127Sep 5, 2023Updated 2 years ago
- ☆11Jun 29, 2021Updated 5 years ago
- HLA typing for Sanger Based Test☆20Apr 7, 2023Updated 3 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆18Mar 10, 2018Updated 8 years ago
- DACE: A Scalable DP-means Algorithm for Clustering Extremely Large Sequence Data☆10May 22, 2016Updated 10 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.
- MFEprimer-2.0: A fast thermodynamics-based program for checking PCR primer specificity☆41Feb 16, 2021Updated 5 years ago
- ☆10Jun 15, 2017Updated 9 years ago
- Microsatellite Instability (MSI) detection using high-throughput sequencing data.☆117Apr 2, 2025Updated last year
- Genome-wide Association Study (GWAS) Tutorial☆41Apr 12, 2019Updated 7 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆75Jun 26, 2023Updated 3 years ago
- Linkage disequlibrium-informed PGT-A (LD-PGTA). A package for detecting genotypic signatures of aneuploidy from extremely low-coverage se…☆19Oct 10, 2022Updated 3 years ago
- Machine Learning with Python☆12Jul 25, 2022Updated 4 years ago
- myVCF: a web-based platform for target and exome mutations data management☆21Apr 13, 2021Updated 5 years ago
- ☆10Jul 7, 2022Updated 4 years ago
- End-to-end encrypted email - Proton Mail • AdSpecial offer: 40% Off Yearly / 80% Off First Month. All Proton services are open source and independently audited for security.
- A MatchMaker Exchange server☆12Jun 1, 2026Updated 3 months ago
- Alleloscope is a method for allele-specific copy number estimation that can be applied to single cell DNA and ATAC sequencing data (separ…☆32Mar 10, 2023Updated 3 years ago
- Basecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files☆124Updated this week
- ☆57Jan 11, 2023Updated 3 years ago
- Clonal structure identification through penalizing pairwise differences☆11Jul 22, 2026Updated last month
- Introductory workshop teaching python for Data Science and Biomedical Machine Learning☆13May 13, 2022Updated 4 years ago
- Pipeline for universal design of target-enrichment probes from various sources of genomic data.☆29Oct 18, 2020Updated 5 years ago