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Pharos: Collating protein information to shed light on the druggable genome.

Authors :
Nguyen DT
Mathias S
Bologa C
Brunak S
Fernandez N
Gaulton A
Hersey A
Holmes J
Jensen LJ
Karlsson A
Liu G
Ma'ayan A
Mandava G
Mani S
Mehta S
Overington J
Patel J
Rouillard AD
Schürer S
Sheils T
Simeonov A
Sklar LA
Southall N
Ursu O
Vidovic D
Waller A
Yang J
Jadhav A
Oprea TI
Guha R
Source :
Nucleic acids research [Nucleic Acids Res] 2017 Jan 04; Vol. 45 (D1), pp. D995-D1002. Date of Electronic Publication: 2016 Nov 29.
Publication Year :
2017

Abstract

The 'druggable genome' encompasses several protein families, but only a subset of targets within them have attracted significant research attention and thus have information about them publicly available. The Illuminating the Druggable Genome (IDG) program was initiated in 2014, has the goal of developing experimental techniques and a Knowledge Management Center (KMC) that would collect and organize information about protein targets from four families, representing the most common druggable targets with an emphasis on understudied proteins. Here, we describe two resources developed by the KMC: the Target Central Resource Database (TCRD) which collates many heterogeneous gene/protein datasets and Pharos (https://pharos.nih.gov), a multimodal web interface that presents the data from TCRD. We briefly describe the types and sources of data considered by the KMC and then highlight features of the Pharos interface designed to enable intuitive access to the IDG knowledgebase. The aim of Pharos is to encourage 'serendipitous browsing', whereby related, relevant information is made easily discoverable. We conclude by describing two use cases that highlight the utility of Pharos and TCRD.<br /> (Published by Oxford University Press on behalf of Nucleic Acids Research 2016. This work is written by (a) US Government employee(s) and is in the public domain in the US.)

Details

Language :
English
ISSN :
1362-4962
Volume :
45
Issue :
D1
Database :
MEDLINE
Journal :
Nucleic acids research
Publication Type :
Academic Journal
Accession number :
27903890
Full Text :
https://doi.org/10.1093/nar/gkw1072