Alternatives and similar repositories for phenopolis_genomics_browser

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

• varfish-org / varfish-server
  VarFish: comprehensive DNA variant analysis for diagnostics and research
  ☆52Updated this week
• macarthur-lab / clinvar
  This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…
  ☆131Updated 5 years ago
• freeseek / gtc2vcf
  Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF
  ☆162Updated 5 months ago
• mvelinder / ped_draw
  Pedigree drawing with ease
  ☆24Updated 4 years ago
• nf-core / raredisease
  Call and score variants from WGS/WES of rare disease patients.
  ☆114Updated this week
• WGLab / Phen2Gene
  Phenotype driven gene prioritization for HPO
  ☆51Updated 4 years ago
• openvar / variantValidator
  Public repository for VariantValidator project
  ☆79Updated 3 weeks ago
• ImperialCardioGenetics / UTRannotator
  VEP Plugin to annotate high-impact five prime UTR variants
  ☆28Updated last year
• grst / snakemake_nextflow_wdl
  simple comparison of snakemake, nextflow and cromwell/wdl
  ☆50Updated 5 years ago
• oncokb / oncokb-annotator
  Annotates variants in MAF with OncoKB annotation.
  ☆141Updated last month
• DECIPHER-genomics / Genoverse
  HTML5 scrollable genome browser
  ☆111Updated 2 years ago
• KarchinLab / open-cravat
  A modular annotation tool for genomic variants
  ☆146Updated last week
• ncbi / dbvar
  dbVar
  ☆40Updated 3 years ago
• WGLab / CancerVar
  Clinical interpretation of somatic mutations in cancer
  ☆50Updated 11 months ago
• ohsu-comp-bio / g2p-aggregator
  Associations of genomic features, drugs and diseases
  ☆48Updated 3 years ago
• phenopolis / phenopolis
  An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data
  ☆33Updated 3 years ago
• PoseyPod / RAG-HPO
  This is the repository for the Python based program for automated deep phenotype analysis of clinical information using large language mo…
  ☆25Updated 4 months ago
• Clinical-Genomics / genmod
  Annotate models of genetic inheritance patterns in variant files (vcf files)
  ☆85Updated last month
• WGLab / PennCNV
  Copy number vaiation detection from SNP arrays
  ☆97Updated last year
• PharmGKB / PharmCAT
  The Pharmacogenomic Clinical Annotation Tool
  ☆158Updated this week
• KalinNonchev / gnomAD_DB
  This package scales the huge gnomAD files to a SQLite database, which is easy and fast to query. It extracts from a gnomAD vcf the minor …
  ☆52Updated last month
• statgen / gotcloud
  Genomes on the Cloud, Mapping & Variant Calling Pipelines
  ☆33Updated 8 years ago
• TheJacksonLaboratory / LIRICAL
  LIkelihood Ratio Interpretation of Clinical AbnormaLities
  ☆34Updated 2 months ago
• 0xTCG / aldy
  Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
  ☆67Updated last month
• broadinstitute / gnomad-browser
  Explore gnomAD datasets on the web
  ☆86Updated this week
• limix / pandas-plink
  PLINK reader for Python.
  ☆89Updated 9 months ago
• PapenfussLab / PathOS
  PathOS is a clinical application for filtering, analysing and reporting on NGS variants
  ☆29Updated 4 years ago
• freeseek / mocha
  MOsaic CHromosomal Alterations (MoChA) caller
  ☆92Updated 5 months ago
• stormliucong / doc2hpo
  ☆33Updated last year
• imgag / megSAP
  a Medical Genetics Sequence Analysis Pipeline
  ☆86Updated this week