Shiny ClinVar web server source code
☆12Apr 29, 2019Updated 6 years ago
Alternatives and similar repositories for Simple-ClinVar
Users that are interested in Simple-ClinVar are comparing it to the libraries listed below
Sorting:
- Website to analyze conflicting assertions in ClinVar☆19Jan 24, 2026Updated last month
- Creating package to draw proteins from Uniprot API☆35Feb 2, 2026Updated last month
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- Interactive table from gemini output☆10Mar 5, 2019Updated 6 years ago
- ProXL Web App -- Visualize and Share Protein Cross-linking Data☆13Feb 23, 2026Updated last week
- Automatically exported from code.google.com/p/kojak-ms☆13Apr 11, 2025Updated 10 months ago
- WIP : regular expressions for identifying and extracting values from HGVS nomenclature☆14Apr 15, 2018Updated 7 years ago
- A reporting pipeline for visualization of immunopeptidomics MS data.☆15Nov 19, 2022Updated 3 years ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 8 years ago
- R-Shiny GUI integrated with the MSstats package family☆20Updated this week
- Code associated with 2019 manuscript entitled "Transcript expression-aware annotation improves rare variant discovery and interpretation…☆34May 5, 2022Updated 3 years ago
- Convert PDB residues to their Uniprot equivalents☆17Mar 31, 2020Updated 5 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Jan 28, 2026Updated last month
- Convert genetic variants to minimal representation☆23Dec 8, 2017Updated 8 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Aug 18, 2020Updated 5 years ago
- LOVD3 development repository☆25Oct 13, 2025Updated 4 months ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 3 years ago
- Python package for investigating the structural context of PTMs☆28Jan 9, 2025Updated last year
- Method for detecting STR expansions from short-read sequencing data☆63Dec 15, 2021Updated 4 years ago
- ☆30May 15, 2025Updated 9 months ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆39Nov 19, 2025Updated 3 months ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆30Feb 20, 2021Updated 5 years ago
- ☆11Aug 10, 2023Updated 2 years ago
- Ensembl tools☆34Nov 3, 2025Updated 4 months ago
- Python bindings to bwa mem☆32Mar 26, 2020Updated 5 years ago
- GraphBio: a shiny web app to easily perform popular visualization analysis for omics data☆33Jul 14, 2023Updated 2 years ago
- CKA 练习环境,适配中国国内网络环境,使用 vagrant 进行管理虚拟机,并使用阿里源☆11Dec 21, 2020Updated 5 years ago
- Biological Relationships - Biorels data preparation infrastructure for biology and drug discovery☆15May 19, 2025Updated 9 months ago
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆91Oct 30, 2025Updated 4 months ago
- The Industrialisation and Professionalisation of Data Science: 12 Questions☆13Aug 12, 2017Updated 8 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Sep 3, 2019Updated 6 years ago
- An easy-to-use and interactive web application for FragPipe☆13Jul 28, 2025Updated 7 months ago
- Proteogenomics database-generation tool for protein haplotypes and variants☆11Jun 19, 2025Updated 8 months ago
- The DNAnexus incremental upload script packaged as an Ansible Role☆13Apr 7, 2025Updated 10 months ago
- Quickomics: exploring omics data in an intuitive, interactive and informative manner. Bioinformatics. 2021 Apr 26:btab255.☆42Updated this week
- Extensible specification for representing and uniquely identifying biological sequence variation☆96Feb 25, 2026Updated last week
- An agile visualization dashboard for R☆19Oct 8, 2021Updated 4 years ago
- Repository for the code and documentation of EveRplot☆13Jul 20, 2023Updated 2 years ago
- ☆11Aug 21, 2024Updated last year