Ó³»­´«Ã½

A team of researchers from the Ó³»­´«Ã½ of MIT and Harvard and institutions in Denmark and the United Kingdom has launched a new resource for mapping protein interaction networks from genetic data. , InWeb_InBioMap (a.k.a, InWeb_IM) includes data on more than half a million protein-protein interactions and can help scientists interpret the biological meaning of data generated from genome-wide association and other large-scale exome sequencing studies of traits or illnesses.

Protein-protein interaction resources (curated by specialists by laboriously extracting proteomic data from the published literature) can help reveal functional networks and target future research. Such resources have been particularly useful for implicating unsuspected pathways in cancer and other conditions fueled by somatic mutations and other genetic alterations. However, the resources available today differ in the number of protein interactions they capture, the organisms they include, and the experimental approaches used to generate the data.

With InWeb_IM, the team — led by Taibo Li and in the Stanley Center for Psychiatric Research at Ó³»­´«Ã½ and Massachusetts General Hospital — have created a large, standardized, and transparent resource particularly well suited for functionally interpreting large genomic data sets. InWeb_IM contains data from eight established protein interaction resources, covering 585,843 interactions and spanning 87% of reviewed human proteins cataloged in (a major protein sequence and annotation resource). In the paper, the team reported that the networks generated with InWeb_IM’s ranked well for accuracy and quality when benchmarked against several of its source databases using and tissue-specific data from .

InWeb_InBioMap is being updated regularly and is available through , as well as through the pathway analysis and visualization platform.