TY - JOUR
T1 - LINCS Data Portal 2.0
T2 - Next generation access point for perturbation-response signatures
AU - Stathias, Vasileios
AU - Turner, John
AU - Koleti, Amar
AU - Vidovic, Dusica
AU - Cooper, Daniel
AU - Fazel-Najafabadi, Mehdi
AU - Pilarczyk, Marcin
AU - Terryn, Raymond
AU - Chung, Caty
AU - Umeano, Afoma
AU - Clarke, Daniel J.B.
AU - Lachmann, Alexander
AU - Evangelista, John Erol
AU - Ma'Ayan, Avi
AU - Medvedovic, Mario
AU - Schürer, Stephan C.
N1 - Funding Information:
National Institutes of Health (NIH) [U54HL127624: BD2K-LINCS Data Coordination and Integration Center, DCIC; U24TR002278: Illuminating the Druggable Genome Resource Dissemination and Outreach Center, IDG-RDOC; U01LM012630]; BD2K-LINCS DCIC is awarded by the National Heart, Lung, and Blood Institute through funds provided by the trans-NIH Library of Integrated Network-based Cellular Signatures (LINCS) Program (http://www.lincsproject.org/) and the trans-NIH Big Data to Knowledge (BD2K) initiative (https://commonfund.nih.gov/bd2k); IDG-RDOC (https: //druggablegenome.net/) is a component of the Illuminating the Druggable Genome (IDG) project (https:// commonfund.nih.gov/idg) awarded by the National Center for Advancing Translational Sciences (NCATS). LINCS, IDG, and BD2K are NIH Common Fund projects. Funding for open access charge: NIH [U54HL127624: BD2K-LINCS Data Coordination and Integration Center, DCIC]. Conflict of interest statement. None declared.
Publisher Copyright:
© 2019 The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - The Library of Integrated Network-Based Cellular Signatures (LINCS) is an NIH Common Fund program with the goal of generating a large-scale and comprehensive catalogue of perturbation-response signatures by utilizing a diverse collection of perturbations across many model systems and assay types. The LINCS Data Portal (LDP) has been the primary access point for the compendium of LINCS data and has been widely utilized. Here, we report the first major update of LDP (http://lincsportal.ccs.miami.edu/signatures) with substantial changes in the data architecture and APIs, a completely redesigned user interface, and enhanced curated metadata annotations to support more advanced, intuitive and deeper querying, exploration and analysis capabilities. The cornerstone of this update has been the decision to reprocess all high-level LINCS datasets and make them accessible at the data point level enabling users to directly access and download any subset of signatures across the entire library independent from the originating source, project or assay. Access to the individual signatures also enables the newly implemented signature search functionality, which utilizes the iLINCS platform to identify conditions that mimic or reverse gene set queries. A newly designed query interface enables global metadata search with autosuggest across all annotations associated with perturbations, model systems, and signatures.
AB - The Library of Integrated Network-Based Cellular Signatures (LINCS) is an NIH Common Fund program with the goal of generating a large-scale and comprehensive catalogue of perturbation-response signatures by utilizing a diverse collection of perturbations across many model systems and assay types. The LINCS Data Portal (LDP) has been the primary access point for the compendium of LINCS data and has been widely utilized. Here, we report the first major update of LDP (http://lincsportal.ccs.miami.edu/signatures) with substantial changes in the data architecture and APIs, a completely redesigned user interface, and enhanced curated metadata annotations to support more advanced, intuitive and deeper querying, exploration and analysis capabilities. The cornerstone of this update has been the decision to reprocess all high-level LINCS datasets and make them accessible at the data point level enabling users to directly access and download any subset of signatures across the entire library independent from the originating source, project or assay. Access to the individual signatures also enables the newly implemented signature search functionality, which utilizes the iLINCS platform to identify conditions that mimic or reverse gene set queries. A newly designed query interface enables global metadata search with autosuggest across all annotations associated with perturbations, model systems, and signatures.
UR - http://www.scopus.com/inward/record.url?scp=85077665017&partnerID=8YFLogxK
U2 - 10.1093/nar/gkz1023
DO - 10.1093/nar/gkz1023
M3 - Article
C2 - 31701147
AN - SCOPUS:85077665017
SN - 0305-1048
VL - 48
SP - D431-D439
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - D1
ER -