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1.
Am J Physiol Renal Physiol ; 312(3): F533-F542, 2017 03 01.
Article in English | MEDLINE | ID: mdl-27974320

ABSTRACT

The organization of the mammalian genome into gene subsets corresponding to specific functional classes has provided key tools for systems biology research. Here, we have created a web-accessible resource called the Mammalian Metabolic Enzyme Database (https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/MetabolicEnzymeDatabase.html) keyed to the biochemical reactions represented on iconic metabolic pathway wall charts created in the previous century. Overall, we have mapped 1,647 genes to these pathways, representing ~7 percent of the protein-coding genome. To illustrate the use of the database, we apply it to the area of kidney physiology. In so doing, we have created an additional database (Database of Metabolic Enzymes in Kidney Tubule Segments: https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/), mapping mRNA abundance measurements (mined from RNA-Seq studies) for all metabolic enzymes to each of 14 renal tubule segments. We carry out bioinformatics analysis of the enzyme expression pattern among renal tubule segments and mine various data sources to identify vasopressin-regulated metabolic enzymes in the renal collecting duct.


Subject(s)
Audiovisual Aids , Databases, Protein , Energy Metabolism , Enzymes/metabolism , Kidney Tubules/enzymology , Protein Interaction Maps , Systems Biology/methods , Animals , Data Mining , Diffusion of Innovation , Enzymes/genetics , Gene Expression Regulation, Enzymologic , Mice , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Vasopressins/metabolism
2.
Am J Physiol Renal Physiol ; 311(4): F787-F792, 2016 10 01.
Article in English | MEDLINE | ID: mdl-27279488

ABSTRACT

Due to recent advances in high-throughput techniques, we and others have generated multiple proteomic and transcriptomic databases to describe and quantify gene expression, protein abundance, or cellular signaling on the scale of the whole genome/proteome in kidney cells. The existence of so much data from diverse sources raises the following question: "How can researchers find information efficiently for a given gene product over all of these data sets without searching each data set individually?" This is the type of problem that has motivated the "Big-Data" revolution in Data Science, which has driven progress in fields such as marketing. Here we present an online Big-Data tool called BIG (Biological Information Gatherer) that allows users to submit a single online query to obtain all relevant information from all indexed databases. BIG is accessible at http://big.nhlbi.nih.gov/.


Subject(s)
Database Management Systems , Databases, Factual , Kidney/physiology , Gene Expression , Humans , Proteome , Proteomics
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