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Cited 16 times in

Systematic analysis of cDNA microarray-based CGH.

DC Field Value Language
dc.contributor.author라선영-
dc.contributor.author안성환-
dc.contributor.author양상화-
dc.contributor.author정현철-
dc.contributor.author정희철-
dc.date.accessioned2015-06-10T11:58:03Z-
dc.date.available2015-06-10T11:58:03Z-
dc.date.issued2006-
dc.identifier.issn1107-3756-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/108946-
dc.description.abstractcDNA microarray-based CGH (Microarray-CGH) is a useful technique for detecting genomic aberrations with a high resolution. However, the criteria for determining a genomic alteration have not been determined. We evaluated the genome-wide measurement of copy number of each gene in normal gastric and placenta tissues with both sex-matched, direct and sex-mismatched, indirect designs using 17K cDNA microarray. The results revealed the range of genomic copy number of normal tissues to be ±0.3 of the log2 ratio (gain >0.3, loss <−0.3) in the autosomal genes with direct and indirect designs. The copy number at a gene level from the X chromosomal genes using the direct and indirect sex-mismatched designs was ±0.68 of the log2 ratio (amplification >0.68, deletion <−0.68). In summary, the suggested method can be used as a guideline for analysis of genomic aberration using a Microarray-CGH in both direct and indirect designs.-
dc.description.statementOfResponsibilityopen-
dc.format.extent261~267-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHChromosomes, Human/genetics-
dc.subject.MESHFemale-
dc.subject.MESHGenome, Human/genetics-
dc.subject.MESHHumans-
dc.subject.MESHIn Situ Hybridization, Fluorescence-
dc.subject.MESHMale-
dc.subject.MESHNucleic Acid Hybridization/methods*-
dc.subject.MESHOligonucleotide Array Sequence Analysis*-
dc.titleSystematic analysis of cDNA microarray-based CGH.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorChan Hee Park-
dc.contributor.googleauthorHa Jin Jeong-
dc.contributor.googleauthorYeon Ho Choi-
dc.contributor.googleauthorSang Cheol Kim-
dc.contributor.googleauthorHei Chul Jeong-
dc.contributor.googleauthorKyu Hyun Park-
dc.contributor.googleauthorGui Yeon Lee-
dc.contributor.googleauthorTae Soo Kim-
dc.contributor.googleauthorSang Wha Yang-
dc.contributor.googleauthorSung Whan Ahn-
dc.contributor.googleauthorYang Seok Kim-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.googleauthorHyun Cheol Chung-
dc.identifier.doi10.3892/ijmm.17.2.261-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02288-
dc.contributor.localIdA03773-
dc.contributor.localIdA02239-
dc.contributor.localIdA01316-
dc.contributor.localIdA03794-
dc.relation.journalcodeJ01132-
dc.identifier.eissn1791-244X-
dc.identifier.pmid16391824-
dc.identifier.urlhttp://www.spandidos-publications.com/ijmm/17/2/261-
dc.contributor.alternativeNameRha, Sun Young-
dc.contributor.alternativeNameAn, Sung Whan-
dc.contributor.alternativeNameYang, Sang Hwa-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.alternativeNameJeung, Hei Cheul-
dc.contributor.affiliatedAuthorYang, Sang Hwa-
dc.contributor.affiliatedAuthorChung, Hyun Cheol-
dc.contributor.affiliatedAuthorAn, Sung Whan-
dc.contributor.affiliatedAuthorRha, Sun Young-
dc.contributor.affiliatedAuthorJeung, Hei Cheul-
dc.rights.accessRightsnot free-
dc.citation.volume17-
dc.citation.number2-
dc.citation.startPage261-
dc.citation.endPage267-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, Vol.17(2) : 261-267, 2006-
dc.identifier.rimsid50357-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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