URL: http://www.scienceexchange.com/facilities/parabase-genomics
Proper Citation: Parabase Genomics (RRID:SCR_012336)
Description: THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 2, 2024. Parabase Genomics is a molecular diagnostic company offering whole exome sequencing services to physicians and researchers with a specialty in the identification of rare variants associated with Mendelian Disorders. Our sample processing and variant analysis pipelines are highly optimized for calling rare variants that are normally missed by less optimized workflows. At Parabase Genomics, we have combined a team of innovators and experts in genomics, pediatrics and targeted sequencing that are not available at other service organizations. Our team is also unique in that we can deliver both research and well as CLIA/CAP certified exomes with insurance reimbursement.
Abbreviations: Parabase Genomics
Resource Type: service resource, commercial organization
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