ncbi / tmVar3Links
☆20Updated 2 years ago
Alternatives and similar repositories for tmVar3
Users that are interested in tmVar3 are comparing it to the libraries listed below
Sorting:
- A phenotype-based tool for variant prioritization in WES and WGS data☆39Updated 2 years ago
- A Python library to work with, analyze, filter and inspect the Human Phenotype Ontology☆28Updated 8 months ago
- ☆25Updated last year
- A combined deep learning tool for automated recognition of human phenotype ontology☆27Updated 2 years ago
- ☆32Updated 10 months ago
- Tool suite for HGVS variant descriptions☆47Updated 3 weeks ago
- phenotype-based prioritization of candidate genes for human diseases☆65Updated 2 years ago
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆87Updated 2 weeks ago
- Clinical interpretation of somatic mutations in cancer☆49Updated 8 months ago
- Platform for Oncogenomic Reporting and Interpretation (PORI)☆35Updated last month
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated last week
- Text-mined knowledgebase for drivers, oncogenes and tumor suppressors in cancer☆41Updated 2 years ago
- Functional Associations using Variational Autoencoders☆40Updated last month
- simplified searching, fetching, and parsing records from NCBI using their E-utilities interface☆63Updated 2 months ago
- A metadata commons to store research software metadata☆44Updated this week
- Associations of genomic features, drugs and diseases☆48Updated 2 years ago
- Phenotype driven gene prioritization for HPO☆50Updated 4 years ago
- Converts Ensembl, Uniprot, and HGNC IDs to Entrez Gene Id☆47Updated 2 years ago
- ☆15Updated 5 months ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- A pipeline that takes clinical notes from EHRs and generate phenotype terms, then generate ranked gene list☆37Updated 2 years ago
- This repository contains Jupyter Notebooks containing GATK Best Practices Workflows☆26Updated 5 years ago
- Reproducible bioinformatics pipelines in python. Import any Unix tool/command in python.☆84Updated 4 years ago
- Rareservoir Database Tools☆16Updated 2 years ago
- Repo for downloading and storing OMIM data☆19Updated 9 years ago
- An information model for representing variant annotations.☆24Updated this week
- ☆31Updated last year
- A Python-based EGA download client☆107Updated last year
- MyGene.info: A BioThings API for gene annotations☆128Updated 2 months ago
- A Python package for pharmacogenomics (PGx) research☆80Updated this week