Clinical DNA Sequencing Analysis and Data Warehouse
☆24Oct 24, 2014Updated 11 years ago
Alternatives and similar repositories for varify
Users that are interested in varify are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- MedSavant is a search engine for genetic variants☆22Apr 21, 2016Updated 10 years ago
- Metadata APIs for Django☆41Oct 22, 2019Updated 6 years ago
- Official client for Harvest (http://harvest.research.chop.edu)☆28Nov 16, 2017Updated 8 years ago
- Harvest CLI and starter project template☆26Oct 23, 2015Updated 10 years ago
- Generate an enhanced VCF files from ClinVar XML Full releases☆17Jul 21, 2026Updated 2 months ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- The original version of MGA has been archived - please see https://github.com/crukci-bioinformatics/mga2 instead.☆24Apr 15, 2021Updated 5 years ago
- STORMSeq: Scalable Tools for Open-source Read Mapping☆19May 19, 2014Updated 12 years ago
- Serrano implements a hypermedia API for Avocado. Avocado is a Django app which targets developers who are interested in letting their dat…☆20Feb 8, 2018Updated 8 years ago
- EXPERIMENTAL implementation of side graph☆10Apr 16, 2015Updated 11 years ago
- robust matching of small variant datasets using flexible scoring schemes☆12Mar 26, 2020Updated 6 years ago
- A configurable de novo assembly pipeline☆30Jun 29, 2016Updated 10 years ago
- ☆13Feb 19, 2017Updated 9 years ago
- Variant Alert!, a framework to monitor every significant alteration in variant classification and gene-disease association between two ve…☆14Jul 19, 2021Updated 5 years ago
- A simple and performant API for working with many genomic file formats in a consistent fashion☆16Mar 23, 2018Updated 8 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Django model relation tree traversal, i.e. automatic joins.☆17Jul 3, 2019Updated 7 years ago
- Hemang Parikh☆11Jan 12, 2016Updated 10 years ago
- A support vector machine for calling variants from next-gen sequencing data☆15Dec 12, 2013Updated 12 years ago
- ☆13Jun 21, 2017Updated 9 years ago
- This project is deprecated, please see strelka2 at https://github.com/Illumina/strelka☆37Feb 24, 2017Updated 9 years ago
- laSV is a software package that employs local assembly to detect structural variations from whole-genome high-throughput sequencing datas…☆12Sep 26, 2016Updated 10 years ago
- The first CHM1 paper (Li, 2014)☆25Jul 9, 2014Updated 12 years ago
- ☆14Jan 20, 2016Updated 10 years ago
- An accelerated framework for manipulating and interpreting high-throughput sequencing data☆26Jul 9, 2013Updated 13 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.
- A Swiss army knife for genome projects☆15Aug 13, 2013Updated 13 years ago
- ☆36Aug 13, 2020Updated 6 years ago
- A small library for ranges/intervals, for use with genomic data.☆17Nov 27, 2012Updated 13 years ago
- Analysis of Ebola virus genomes☆17May 18, 2015Updated 11 years ago
- Use somatic mutations to choose a personalized cancer vaccine (tumor-specific immunogenic peptides)☆16Sep 23, 2016Updated 10 years ago
- Population Reference Graphs for the HLA and MHC.☆35Dec 18, 2018Updated 7 years ago
- Variant Caller Analysis Dashboard and Data Management System☆36Feb 8, 2016Updated 10 years ago
- Fast and Accurate Classification of Sequences using Bloom filters☆16Apr 19, 2023Updated 3 years ago
- Concordance between variant callers☆17Nov 27, 2014Updated 11 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.
- Utilities for analyzing mutations and neoepitopes in patient cohorts☆20Jun 7, 2018Updated 8 years ago
- Convert genetic variants to minimal representation☆23Dec 8, 2017Updated 8 years ago
- Compressive Read-mapping Accelerator☆14Sep 7, 2016Updated 10 years ago
- A python script used to annotate genomic intervals.☆18May 29, 2020Updated 6 years ago
- commandline manipulation of genomic variants and NGS reads☆20Sep 6, 2024Updated 2 years ago
- Genotype + Environment = Trait Evidence (GET-E) Database: help the Personal Genome Project, the clinical genetics community, and, the gen…☆26Oct 23, 2012Updated 13 years ago
- An OCaml RocksDb binding using ocaml-ctypes☆28Jun 14, 2019Updated 7 years ago