Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Nucleic Acids Research |
| Vol/bind | 38 |
| Udgave nummer | Database issue |
| Sider (fra-til) | D699-702 |
| ISSN | 0305-1048 |
| DOI | |
| Status | Udgivet - 2010 |
Bibliografisk note
Keywords: Algorithms; Animals; Cell Cycle; Computational Biology; Databases, Genetic; Databases, Nucleic Acid; Databases, Protein; Gene Expression Profiling; Genome; Humans; Information Storage and Retrieval; Internet; Oligonucleotide Array Sequence Analysis; SoftwareAdgang til dokumentet
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I: Nucleic Acids Research, Bind 38, Nr. Database issue, 2010, s. D699-702.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Cyclebase.org: version 2.0, an updated comprehensive, multi-species repository of cell cycle experiments and derived analysis results
AU - Gauthier, Nicholas Paul
AU - Jensen, Lars Juhl
AU - Wernersson, Rasmus
AU - Brunak, Søren
AU - Jensen, Thomas S
N1 - Keywords: Algorithms; Animals; Cell Cycle; Computational Biology; Databases, Genetic; Databases, Nucleic Acid; Databases, Protein; Gene Expression Profiling; Genome; Humans; Information Storage and Retrieval; Internet; Oligonucleotide Array Sequence Analysis; Software
PY - 2010
Y1 - 2010
N2 - Cell division involves a complex series of events orchestrated by thousands of molecules. To study this process, researchers have employed mRNA expression profiling of synchronously growing cell cultures progressing through the cell cycle. These experiments, which have been carried out in several organisms, are not easy to access, combine and evaluate. Complicating factors include variation in interdivision time between experiments and differences in relative duration of each cell-cycle phase across organisms. To address these problems, we created Cyclebase, an online resource of cell-cycle-related experiments. This database provides an easy-to-use web interface that facilitates visualization and download of genome-wide cell-cycle data and analysis results. Data from different experiments are normalized to a common timescale and are complimented with key cell-cycle information and derived analysis results. In Cyclebase version 2.0, we have updated the entire database to reflect changes to genome annotations, included information on cyclin-dependent kinase (CDK) substrates, predicted degradation signals and loss-of-function phenotypes from genome-wide screens. The web interface has been improved and provides a single, gene-centric graph summarizing the available cell-cycle experiments. Finally, key information and links to orthologous and paralogous genes are now included to further facilitate comparison of cell-cycle regulation across species. Cyclebase version 2.0 is available at http://www.cyclebase.org.
AB - Cell division involves a complex series of events orchestrated by thousands of molecules. To study this process, researchers have employed mRNA expression profiling of synchronously growing cell cultures progressing through the cell cycle. These experiments, which have been carried out in several organisms, are not easy to access, combine and evaluate. Complicating factors include variation in interdivision time between experiments and differences in relative duration of each cell-cycle phase across organisms. To address these problems, we created Cyclebase, an online resource of cell-cycle-related experiments. This database provides an easy-to-use web interface that facilitates visualization and download of genome-wide cell-cycle data and analysis results. Data from different experiments are normalized to a common timescale and are complimented with key cell-cycle information and derived analysis results. In Cyclebase version 2.0, we have updated the entire database to reflect changes to genome annotations, included information on cyclin-dependent kinase (CDK) substrates, predicted degradation signals and loss-of-function phenotypes from genome-wide screens. The web interface has been improved and provides a single, gene-centric graph summarizing the available cell-cycle experiments. Finally, key information and links to orthologous and paralogous genes are now included to further facilitate comparison of cell-cycle regulation across species. Cyclebase version 2.0 is available at http://www.cyclebase.org.
U2 - 10.1093/nar/gkp1044
DO - 10.1093/nar/gkp1044
M3 - Journal article
C2 - 19934261
SN - 0305-1048
VL - 38
SP - D699-702
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - Database issue
ER -