An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases = 단일염기다형성과 질병 연구를 위한 통합 데이터베이스 및 파이프라인 시스템

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dc.contributor.authorJin Ok Yang-
dc.contributor.authorS Hwang-
dc.contributor.authorJung Soo Oh-
dc.contributor.authorJong Hwa Park-
dc.contributor.authorT K Sohn-
dc.date.accessioned2017-04-19T09:12:22Z-
dc.date.available2017-04-19T09:12:22Z-
dc.date.issued2008-
dc.identifier.issn1471-2105-
dc.identifier.uri10.1186/1471-2105-9-S12-S19ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8726-
dc.description.abstractBackground: Studies on the relationship between disease and genetic variations such as single nucleotide polymorphisms (SNPs) are important. Genetic variations can cause disease by influencing important biological regulation processes. Despite the needs for analyzing SNP and disease correlation, most existing databases provide information only on functional variants at specific locations on the genome, or deal with only a few genes associated with disease. There is no combined resource to widely support gene-, SNP-, and disease-related information, and to capture relationships among such data. Therefore, we developed an integrated database-pipeline system for studying SNPs and diseases. Results: To implement the pipeline system for the integrated database, we first unified complicated and redundant disease terms and gene names using the Unified Medical Language System (UMLS) for classification and noun modification, and the HUGO Gene Nomenclature Committee (HGNC) and NCBI gene databases. Next, we collected and integrated representative databases for three categories of information. For genes and proteins, we examined the NCBI mRNA, UniProt, UCSC Table Track and MitoDat databases. For genetic variants we used the dbSNP, JSNP, ALFRED, and HGVbase databases. For disease, we employed OMIM, GAD, and HGMD databases. The database-pipeline system provides a disease thesaurus, including genes and SNPs associated with disease. The search results for these categories are available on the web page http://diseasome.kobic.re.kr/, and a genome browser is also available to highlight findings, as well as to permit the convenient review of potentially deleterious SNPs among genes strongly associated with specific diseases and clinical phenotypes. Conclusion: Our system is designed to capture the relationships between SNPs associated with disease and disease-causing genes. The integrated database-pipeline provides a list of candidate genes and SNP markers for evaluation in both epidemiological and molecular biological approaches to diseases-gene association studies. Furthermore, researchers then can decide semi-automatically the data set for association studies while considering the relationships between genetic variation and diseases. The database can also be economical for disease-association studies, as well as to facilitate an understanding of the processes which cause disease. Currently, the database contains 14,674 SNP records and 109,715 gene records associated with human diseases and it is updated at regular intervals.-
dc.publisherSpringer-BMC-
dc.titleAn integrated database-pipeline system for studying single nucleotide polymorphisms and diseases = 단일염기다형성과 질병 연구를 위한 통합 데이터베이스 및 파이프라인 시스템-
dc.title.alternativeAn integrated database-pipeline system for studying single nucleotide polymorphisms and diseases-
dc.typeArticle-
dc.citation.titleBMC Bioinformatics-
dc.citation.numberS12-
dc.citation.endPageS19-
dc.citation.startPageS19-
dc.citation.volume9-
dc.contributor.affiliatedAuthorJin Ok Yang-
dc.contributor.affiliatedAuthorJung Soo Oh-
dc.contributor.affiliatedAuthorJong Hwa Park-
dc.contributor.alternativeName양진옥-
dc.contributor.alternativeName황소현-
dc.contributor.alternativeName오정수-
dc.contributor.alternativeName박종화-
dc.contributor.alternativeName손태권-
dc.identifier.bibliographicCitationBMC Bioinformatics, vol. 9, no. S12, pp. S19-S19-
dc.identifier.doi10.1186/1471-2105-9-S12-S19-
dc.description.journalClassY-
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