Alternatives and similar repositories for Science-Citation-Knowledge-Extractor

Users that are interested in Science-Citation-Knowledge-Extractor are comparing it to the libraries listed below

• DataBiosphere / data-browser
  ☆11Updated last week
• DataBiosphere / data-explorer
  ☆11Updated 2 years ago
• NCBI-Hackathons / phenotypeXpression
  Subclassification of disease states based on the intersection of literature and expression
  ☆12Updated 6 years ago
• marcos-diazg / musica
  MuSiCa - Mutational Signatures in Cancer
  ☆23Updated last year
• geneontology / helpdesk
  The Gene Ontology Helpdesk
  ☆16Updated 9 months ago
• bihealth / sodar-core-legacy
  LEGACY repository for SODAR Core, preserved for saving review-related issues. See "sodar-core" for the up-to-date repository.
  ☆15Updated 3 years ago
• icgc-dcc / dcc-portal
  Data portal for exploring and accessing data
  ☆16Updated 2 years ago
• NCBI-Hackathons / FlowBio
  A fast, easy way to present complex bioinformatics pipelines to biologists
  ☆11Updated 7 years ago
• idekerlab / ddot
  Toolkit for constructing, analyzing, and visualizing data-driven ontologies
  ☆17Updated 2 years ago
• WGLab / EHR-Phenolyzer
  A pipeline that takes clinical notes from EHRs and generate phenotype terms, then generate ranked gene list
  ☆37Updated 2 years ago
• NCBI-Hackathons / PubRunner
  Framework for running text mining tools on latest publications. Main page at:
  ☆14Updated 3 years ago
• MaayanLab / FAIRshake
  ☆10Updated 2 months ago
• solvebio / veppy
  Variant Effect Prediction for Python
  ☆15Updated 8 years ago
• Genomon-Project / paplot
  paplot creates various dynamic and interactive reports for cancer genome analysis.
  ☆25Updated 2 years ago
• AbbVie-ComputationalGenomics / genetic-evidence-approval
  ☆26Updated 4 years ago
• NCBI-Hackathons / Bringing-the-Power-of-Synthetic-Data-Generation-to-the-Masses
  We aim to make it easier for biomedical researchers to access and customize synthetic sequence data for the purpose of sharing and testin…
  ☆11Updated 6 years ago
• ccmbioinfo / crg2
  Research pipeline for exploring clinically relevant genomic variants
  ☆16Updated last week
• PreMedKB / PAnno
  PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.
  ☆15Updated 2 years ago
• raulossio / VCF-plotein
  Visualisation and prioritisation of genomic variants from human exome sequencing projects
  ☆13Updated 6 years ago
• bmeg / funnel-client
  Trigger the Google Genomics Pipeline API with CWL
  ☆11Updated 8 years ago
• kkdey / aRchaic
  Exploration, clustering, visualization and classification of DNA damage patterns
  ☆19Updated 4 years ago
• biocompute-objects / BCO_Documentation
  Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:
  ☆17Updated last year
• Steven-N-Hart / VariantDB_Challenge
  Finding a scalable alternative to the VCF File for genomics analysis
  ☆14Updated 8 years ago
• atgu / aou_gwas
  ☆12Updated 2 weeks ago
• NCBI-Hackathons / Pharmacogenomics_Prediction_Pipeline_P3
  ☆28Updated 7 years ago
• raphael-group / magi
  A web application from the Raphael Lab for mutation annotation and genome interpretation.
  ☆20Updated 7 years ago
• fairgenomes / fairgenomes-semantic-model
  FAIR Genomes semantic metadata model. The core is a YAML file, which is transformed into all other desired output formats.
  ☆13Updated last week
• sigven / pharmOncoX
  Targeted and non-targeted anticancer drugs and drug regimens
  ☆29Updated last week
• Bohdan-Khomtchouk / PubData
  Smart search engine for all bioinformatics databases worldwide
  ☆27Updated 7 years ago
• omicidx / omicidx-parsers
  Exposing public genomics data via computable and searchable metadata
  ☆13Updated last year