Our software tools help principal investigators, core facilities, and enterprise bioinformatics teams analyze gene expression data (e.g. RNA-Seq or microarray) and variant data (e.g. DNA-Seq) to find biomarkers, identify impacted pathways, and pinpoint putative mechanisms. Currently, this frustrating process is slow, unreliable, expensive, and often requires multiple disjointed tools, which then provide irrelevant or incorrect results. While other solutions drop a haystack of results on you, we lead you straight to the needle.
Who We Serve
Each of our customers uses one or more of the following products to address their individual challenges.
Import your RNA-Seq data and identify significant pathways and mechanisms
without all the noise found
in other approaches.
Import your VCF file and identify causal variants and biological
impact in minutes leveraging a systems biology approach.
Google for Scientists!
28,353,480 references, 7,705,042 interactions, and 401,213 supporting experiments at your fingertips for free.