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The Mastermind Cited Variants Reference (CVR) contains annotations with the
number of articles for each variant cited in the medical literature. This
public dataset is most commonly used as an evidence filter for clinical
actionability in genomic analysis pipelines (based on presence or lack of
evidence in the literature) and a quick way to get insight into the literature
for variant curation through links into the Mastermind Genomic Search Engine.
Dataset access
BigQuery datasets
You can access the following dataset in BigQuery for data
exploration and querying. The dataset contains separate tables with annotations
using build GRCh37 and GRCh38. Genomenon hosts a
public repository with
convenience scripts and information about how to directly annotate your variant
data with the annotations from the public dataset.
Use: This dataset is publicly available for anyone to use under the
terms provided by the dataset source
(https://www.genomenon.com/cvr/)
and is provided "AS IS" without any warranty, express or implied, from Google.
Google disclaims all liability for any damages, direct or indirect, resulting
from the use of the dataset.
[[["Easy to understand","easyToUnderstand","thumb-up"],["Solved my problem","solvedMyProblem","thumb-up"],["Other","otherUp","thumb-up"]],[["Hard to understand","hardToUnderstand","thumb-down"],["Incorrect information or sample code","incorrectInformationOrSampleCode","thumb-down"],["Missing the information/samples I need","missingTheInformationSamplesINeed","thumb-down"],["Other","otherDown","thumb-down"]],["Last updated 2025-01-28 UTC."],[],[]]
