☆41Mar 2, 2026Updated last week
Alternatives and similar repositories for aws-healthomics-tools
Users that are interested in aws-healthomics-tools are comparing it to the libraries listed below
Sorting:
- Linter rules for Nextflow DSL scripts☆34Feb 16, 2026Updated 3 weeks ago
- ☆89Feb 23, 2026Updated 2 weeks ago
- This project contains the webapp sample integrated with AWS HealthOmics, which allows users such as admin and bioinformaticians to operat…☆19Nov 20, 2024Updated last year
- Library for indexing VCF files for random access searches by rsID☆17Mar 2, 2026Updated last week
- Binding Affinity Prediction using Deep learning models☆12Jun 9, 2021Updated 4 years ago
- AWS Biotech Blueprint Multi-Account☆12Jul 22, 2020Updated 5 years ago
- ☆31Jan 9, 2026Updated 2 months ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Apr 23, 2019Updated 6 years ago
- Cromwell output organizer☆13May 18, 2021Updated 4 years ago
- FireCloud Service Selector (FISS) -- Python bindings and CLI for FireCloud execution engine☆34Jan 13, 2026Updated last month
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- A tool set to assess the quality of the per read phasing and reduce the errors.☆13Jun 25, 2020Updated 5 years ago
- ☆12Oct 13, 2021Updated 4 years ago
- Easily run WDL workflows on GCP☆14Sep 28, 2021Updated 4 years ago
- add true-negative SVs from a population callset to a truth-set.☆15Jun 17, 2022Updated 3 years ago
- RNA Fusion Detection and Quantification☆18Oct 31, 2018Updated 7 years ago
- Classes for storing very large GWAS data sets and annotation, and functions for GWAS data cleaning and analysis☆18Mar 18, 2025Updated 11 months ago
- A python tool for parsing pedigree files☆16Aug 29, 2017Updated 8 years ago
- ☆114Dec 16, 2025Updated 2 months ago
- Genomics Workflows on AWS☆146Jul 31, 2023Updated 2 years ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆18Apr 2, 2020Updated 5 years ago
- A series of tools and pipelines for genotyping MHC / HLA genes and alleles using SMRT Sequencing☆22Aug 29, 2016Updated 9 years ago
- Template for building your own portfolio☆27Jul 2, 2025Updated 8 months ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Dec 6, 2023Updated 2 years ago
- A Standard Database for Drug Repositioning☆19Jul 28, 2017Updated 8 years ago
- ☆23Nov 9, 2025Updated 4 months ago
- use the noise☆15Apr 15, 2020Updated 5 years ago
- Use R to generate a database containing the UK Biobank data schemas from http://biobank.ctsu.ox.ac.uk/crystal/schema.cgi☆20Feb 26, 2021Updated 5 years ago
- ☆20Sep 25, 2020Updated 5 years ago
- Lossless VCF compression☆21Mar 4, 2022Updated 4 years ago
- Multi-omics data normalisation, model fitting and visualisation.☆27Apr 6, 2023Updated 2 years ago
- ☆21Jul 6, 2023Updated 2 years ago
- Using k-mers to call HLA alleles in RNA sequencing data☆23Jul 26, 2018Updated 7 years ago
- ☆148May 6, 2024Updated last year
- AirLift is a tool that updates mapped reads from one reference genome to another. Unlike existing tools, It accounts for regions not shar…☆28May 23, 2024Updated last year
- Variant catalogue pipeline☆26Jan 30, 2026Updated last month
- A tool for summarizing, extracting, generating and modifying DNA sequences.☆23Dec 17, 2024Updated last year
- ☆27Jun 5, 2025Updated 9 months ago
- Evaluation of phasing performance☆23Mar 6, 2018Updated 8 years ago