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英文字典中文字典相关资料:


  • ClinVar - National Center for Biotechnology Information
    ClinVar aggregates information about genomic variation and its relationship to human health
  • ClinVar - ClinGen | Clinical Genome Resource
    ClinVar is a a freely accessible, public archive of reports of the relationships among human variations and phenotypes hosted by the National Center for Biotechnology Information (NCBI) and funded by intramural National Institutes of Health (NIH) funding
  • NCBI ClinVar - National Library of Medicine
    The NCBI ClinVar database collects reports from scientists on human genetic variants and their relationships to disease Its purpose is to bridge genetic variation data and observations or assertions about phenotypes that are related to those variations
  • FAQ about using ClinVar - ncbi. xyz
    ClinVar is an archive for classification made by our submitters Submitters may disagree on how a variant should be classified; read more about how ClinVar calculates consensus and conflicts in different types of classifications ClinVar does not arbitrate and resolve these conflicts
  • Simple ClinVar
    Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database Nucleic Acids Research (2019) PMID:31114901
  • ClinVar: public archive of interpretations of clinically relevant . . .
    ClinVar is an archival database, maintaining a history of updates from a single submitter, as well as retaining a distinction among content from different submitters for the same variant or variant-condition interpretation, each with its own interpretation and supporting evidence
  • What information can I find in the ClinVar database?
    ClinVar is one of the three NCBI databases that are intended for healthcare professionals and researchers who are focusing on genetic disease It contains information about genomic variations and their relationships to human health
  • What Is the ClinVar Database and How Is It Used?
    The ClinVar database is a public resource that catalogs the relationships between human genetic variations and health Managed by the National Center for Biotechnology Information (NCBI), this freely accessible archive serves as a global repository for information on how specific changes in our DNA are connected to diseases
  • Using ClinVar as a Resource to Support Variant Interpretations
    ClinVar is a freely accessible, public archive of reports of the relationships among genomic variants and phenotypes To facilitate evaluation of the clinical significance of each variant, ClinVar aggregates submissions of the same variant, displays





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