Inferring Higher Functional Information for RIKEN Mouse Full-Length cDNA Clones With FACTS
Open Access
- 2 June 2003
- journal article
- Published by Cold Spring Harbor Laboratory in Genome Research
- Vol. 13 (6b) , 1520-1533
- https://doi.org/10.1101/gr.1019903
Abstract
FACTS (Functional Association/Annotation of cDNA Clones from Text/Sequence Sources) is a semiautomated knowledge discovery and annotation system that integrates molecular function information derived from sequence analysis results (sequence inferred) with functional information extracted from text. Text-inferred information was extracted from keyword-based retrievals of MEDLINE abstracts and by matching of gene or protein names to OMIM, BIND, and DIP database entries. Using FACTS, we found that 47.5% of the 60,770 RIKEN mouse cDNA FANTOM2 clone annotations were informative for text searches. MEDLINE queries yielded molecular interaction-containing sentences for 23.1% of the clones. When disease MeSH and GO terms were matched with retrieved abstracts, 22.7% of clones were associated with potential diseases, and 32.5% with GO identifiers. A significant number (23.5%) of disease MeSH-associated clones were also found to have a hereditary disease association (OMIM Morbidmap). Inferred neoplastic and nervous system disease represented 49.6% and 36.0% of disease MeSH-associated clones, respectively. A comparison of sequence-based GO assignments with informative text-based GO assignments revealed that for 78.2% of clones, identical GO assignments were provided for that clone by either method, whereas for 21.8% of clones, the assignments differed. In contrast, for OMIM assignments, only 28.5% of clones had identical sequence-based and text-based OMIM assignments. Sequence, sentence, and term-based functional associations are included in the FACTS database (http://facts.gsc.riken.go.jp/), which permits results to be annotated and explored through web-accessible keyword and sequence search interfaces. The FACTS database will be a critical tool for investigating the functional complexity of the mouse transcriptome, cDNA-inferred interactome (molecular interactions), and pathome (pathologies).Keywords
This publication has 41 references indexed in Scilit:
- Human Disease Genes and Their Cloned Mouse Orthologs: Exploration of the FANTOM2 cDNA Sequence Data SetGenome Research, 2003
- The Mammalian Protein–Protein Interaction Database and Its Viewing System That Is Linked to the Main FANTOM2 ViewerGenome Research, 2003
- Impact of Alternative Initiation, Splicing, and Termination on the Diversity of the mRNA Transcripts Encoded by the Mouse TranscriptomeGenome Research, 2003
- Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAsNature, 2002
- Initial sequencing and comparative analysis of the mouse genomeNature, 2002
- Cell-Type-Dependent Induction of eotaxin and CCR3 by Ionizing RadiationBiochemical and Biophysical Research Communications, 2000
- Cloning and characterization of hurpin (protease inhibitor 13): a new skin-specific, UV-repressible serine proteinase inhibitor of the ovalbumin serpin familyJournal of Molecular Biology, 1999
- Comparison of DNA Sequences with Protein SequencesGenomics, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Regulation of Epidermal Expression of Keratin K17 in Inflammatory Skin DiseasesJournal of Investigative Dermatology, 1996