Alternatives and similar repositories for fast_hpo_cr

Users that are interested in fast_hpo_cr are comparing it to the libraries listed below

• TheJacksonLaboratory / LIRICAL
  LIkelihood Ratio Interpretation of Clinical AbnormaLities
  ☆29Updated 2 months ago
• bio-ontology-research-group / phenomenet-vp
  A phenotype-based tool for variant prioritization in WES and WGS data
  ☆38Updated 2 years ago
• krishnanlab / txt2onto
  Code for classifying unstructured text to tissue ontology terms using natural language processing and machine learning.
  ☆25Updated last year
• ga4gh / va-spec
  An information model for representing variant annotations.
  ☆21Updated 2 weeks ago
• anergictcell / pyhpo
  A Python library to work with, analyze, filter and inspect the Human Phenotype Ontology
  ☆28Updated 5 months ago
• mikelkou / fava
  Functional Associations using Variational Autoencoders
  ☆40Updated 2 weeks ago
• EBISPOT / EFO-UKB-mappings
  ☆17Updated 6 years ago
• opentargets / gentropy
  Open Targets python framework for post-GWAS analysis
  ☆41Updated last week
• LieberInstitute / recount3
  Explore and download data from the recount3 project
  ☆36Updated 3 months ago
• AbbVie-ComputationalGenomics / genetic-evidence-approval
  ☆25Updated 4 years ago
• astrazeneca-cgr-publications / JARVIS
  JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes
  ☆23Updated 7 months ago
• astrazeneca-cgr-publications / mantis-ml-release
  mantis-ml: Stochastic semi-supervised learning to prioritise genes from high throughput genomic screens
  ☆30Updated last year
• EBISPOT / gwas-summary-statistics-standard
  Documentation on new GWAS Summary Statistics Standard
  ☆21Updated last year
• ericminikel / genetic_support
  Refining the impact of genetic evidence on clinical success
  ☆26Updated last year
• macarthur-lab / omim
  Repo for downloading and storing OMIM data
  ☆19Updated 8 years ago
• ccf-tfehlmann / ibdplexus
  This package helps wrangle the clinical data in IBD Plexus. IBD Plexus is a data exchange platform designed to accelerate research toward…
  ☆16Updated last week
• monarch-initiative / Squirls
  Interpretable prioritization of splice variants in diagnostic next-generation sequencing
  ☆18Updated last year
• Ensembl / postgap
  Linking GWAS studies to genes through cis-regulatory datasets
  ☆39Updated 2 years ago
• sigven / oncoEnrichR
  Explore the cancer relevance of your gene list
  ☆51Updated 5 months ago
• montilab / nf-gwas-pipeline
  A Nextflow Genome-Wide Association Study (GWAS) Pipeline
  ☆35Updated 2 months ago
• WGLab / phenolyzer
  phenotype-based prioritization of candidate genes for human diseases
  ☆65Updated 2 years ago
• sigven / vcf2tsvpy
  Genomic VCF to tab-separated values
  ☆47Updated 2 years ago
• mvelinder / ped_draw
  Pedigree drawing with ease
  ☆24Updated 3 years ago
• salbrec / seqQscorer
  ☆22Updated 3 months ago
• bcgsc / pori
  Platform for Oncogenomic Reporting and Interpretation (PORI)
  ☆33Updated last year
• chess-genome / chess
  Comprehensive Human Expressed SequenceS
  ☆18Updated last month
• stjude / proteinpaint
  Data visualization and analysis framework focused on phenotype-molecular data integration at cohort level.
  ☆33Updated this week
• statgen / gotcloud
  Genomes on the Cloud, Mapping & Variant Calling Pipelines
  ☆35Updated 8 years ago
• GMOD / jbrowse-jupyter
  A python package for showing JBrowse views
  ☆26Updated last year
• macarthur-lab / gnomad_browser
  gnomAD browser pre-ASHG 2018
  ☆33Updated 4 years ago