Abstract | Additionally, CSNAP is capable of integrating with biological knowledge-based databases (Uniprot, GO) and high-throughput biology platforms (proteomic, genetic, etc) for system-wise drug target validation. |
Author Summary | Determining the targets of compounds identified in cell-based high-throughput chemical screens is a critical step for downstream drug development and understanding of compound mechanism of action. |
CSNAP validation using benchmark compounds | This indicated that CSNAP could potentially be used for high-throughput target deorphanization and off-target prediction for bioactive compounds from any chemical screen. |
Introduction | Additionally, CSNAP is capable of integrating with chemical and biological knowledge-based databases (Uniprot, GO) and high-throughput biology platforms (proteomic, genetic, etc) for system-wise drug target validation. |
Target prediction of mitotic compounds from chemical screen | Recently, we performed a high-throughput cell-cycle modulator screen with a diverse, unbiased set of 90,000 drug-like compounds, which identified compounds arresting cancer cells in mitosis (212 compounds) (S2, S3 Tables and 81 Text). |
Interactome construction | Binary interactions: We combine several yeast-two-hybrid high-throughput datasets [10,39—42] with binary interactions from IntAct [43] and MINT [44] databases. |
Interactome construction | Signaling interactions: The dataset from [50] provides 32,706 interactions between 6,339 proteins that integrate several sources, both high-throughput and literature curation, into a directed network in which cellular signals are transmitted by proteins-protein interactions. |
Introduction | With recent advances in genome-wide disease gene association [9] and high-throughput Interactome mapping [10] we can already pinpoint the approximate location for some disease modules (Fig. |
Discussion | Data are increasingly become available for the adoption of such classification techniques since high-throughput methods have been recently applied at low cost. |
Discussion | Our work paves the way towards the use of high-throughput expression datasets to a broad range of applications including detection and characterization of the environmental conditions and bacterial population that are important for clinical, environmental, industrial, and agricultural applications. |
Introduction | Indeed, after aggregating all high-throughput transcriptional data that is currently available for E. coli, the most well-studied model microbe, we are still limited to a few thousands microarray or RNA-Seq experiments that cover more than 30 strains, a dozen different media and a multitude of other genetic (knockout, over-expressions, re-wirings), or environmental (carbon limitation, chemicals, abiotic factors) perturbations. |