Streamline Genomics Launches New SeeqVCF VCF Analysis Application, Bringing A Lightweight, Secure VCF Analysis Application to Clinical Genomics Users
MONTREAL, Nov. 1, 2021 /PRNewswire/ -- Streamline Genomics is pleased to announce the launch of SeeqVCF, a lightweight and innovative Variant Call Format ("VCF") filtering application for users of clinical genomics. VCF analysis is a critical component of genomic analysis
This launch comes soon after the September launch of Streamline's Seeq.bio search engine which allows for fast, intuitive search across a wide breadth of genomic information including the ability to cross-reference specific variants against treatments, diseases and — soon — active clinical trials. Both Seeq.bio and SeeqVCF are free to use for individual users, with enterprise-level licenses available for larger teams and power users.
Several factors make VCF analysis difficult:
SeeqVCF specifically addresses these challenges with innovations in how services are distributed and run by the user:
"I am pleased to see us add this amazing innovation to the suite of tools we are offering to users of clinical genomic data." said CEO Curtis Duggan, "Our mission to democratize access to fast, evidence-based genomic analysis is only just beginning."
View original content:https://www.prnewswire.com/news-releases/streamline-genomics-launches-new-seeqvcf-vcf-analysis-application-bringing-a-lightweight-secure-vcf-analysis-application-to-clinical-genomics-users-301412268.html
SOURCE Streamline Genomics