For researchers
For academic, pharmaceutical, and biotech researchers, we offer two services:
knomeBASE is a compute-intensive informatics service that transforms human genome sequence data into a format optimized for fast interpretation. Designed to help geneticists identify the variants, genes, and pathways that govern human disease and drug response, knomeBASE has two components:
Informatics: knomeBASE standardizes, annotates, compares, and distills raw sequence data—addressing the primary informatics challenges that often bottleneck the process of interpreting multiple genomes.
Tool kit: knomeBASE clients receive easy-to-use genome interpretation applications, libraries, and scripts that enable flexible querying, rapid hypothesis testing, data visualization, and custom software development.
knomeDISCOVERY is a complete genome interpretation solution for researchers. It includes whole genome sequencing, project-driven curation, sophisticated informatics, and in-depth interpretation by Knome’s team of experienced geneticists. knomeDISCOVERY is for researchers who seek to outsource the bioinformatics and genetics needed for whole genome studies of human disease or drug response.
For clinics and hospitals
Our platform group provides clinics with large-scale information systems to 1) manage whole genome sequence data and 2) help physicians interpret genomes in order to inform preventative, diagnostic, and treatment decisions.
We partner with leading institutions to incorporate human genomics into clinical care. These relationships take the form of long-term relationships that include highly customized, locally installed versions of our informatics engine, curated databases, and physician-facing applications. To learn more, contact Ari Kiirikki at (617) 715-1000 x6002 or akiirikki@knome.com.
