VarSome.com is a community-driven project aimed at sharing global expertise on human variants. It features a robust aggregated knowledge base consisting of over 140 cross-referenced data resources and contributions from its community of more than 500 000
The results are specific to the contents of the VarSome database, including entries submitted by our user community, and are generally very different from what you would get from a generic web search. We have included a link to google so you can always try VarSome first....
向量数据库(Vector Database),也叫矢量数据库,主要用来存储和处理向量数据。 在数学中,向量是有大小和方向的量,可以使用带箭头的线段表示,箭头指向即为向量的方向,线段的长度表示向量的大小。两个向量的距离或者相似性可以通过汉明距离、欧式距离或者余弦距离得到。 图像、文本和音视频这种非结构化数据都可以通过某种变...
Insertion:https://api.varsome.com/lookup/7-151945072--T?add-ACMG-annotation=1 All the annotation data is returned as a single dictionary, keyed by each source institution & database name. Example keys are "icgc_somatic", "iarc_tp53_germline" and "ncbi_clinvar"....
The current database was last updated on version30-May-2022(1.56M records). For each variant we record its original “source” classification, allele frequency and coding impact. We also re-classify the variants using our implementation of the ACMG rules, with the clinical evidence rules (PS3...
Under VarSome Premium you get access to additional data resources that contain pharmaceutical and clinical trial information or require a license, allowing you to obtain more comprehensive results. Premium Data Resources: AACT Clinical Trials from clinicaltrials.gov Pharmacogenomics Knowledge Base (PharmGKB...
For AR inheritance only, PM2 is triggered if the number of homozygous individuals in the gnomAD database is fewer than three. The same thresholds are used to assign the BS2 criterion [i.e., “Observed in a healthy adult for a recessive (homozygous), dominant (heterozygous), or X-linked ...
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The current database was last updated on version 30-May-2022 (1.56M records). For each variant we record its original “source” classification, allele frequency and coding impact. We also re-classify the variants using our implementation of the ACMG rules, with the clinical evidence rules (PS...