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SNV screening system V.2025

Upgrade the public SNV data used for SNV filtering to a more powerful version!

The "SNV screening system V.2025" is a web analysis system that detects candidate genes from SNV information of multiple samples. It stores the called SNV information of multiple samples in a relational database, allowing users to set various filtering conditions via the web and perform searches, enabling the listing of candidate genes related to phenotypes. The data of the called SNVs is imported into the RDB, followed by preprocessing for annotation assignment and filtering searches. 【Features】 ■ Import SNV data (in VCF format) into RDB ■ Create unique variant data ■ Curated annotation information ■ Grouping of search target samples and saving of search conditions, as well as the ability to perform set operations on SNVs *For more details, please refer to the PDF document or feel free to contact us.

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