<P><B>Summary:</B> Despite a growing interest in a correlation between copy number variations (CNVs) and flanking single nucleotide polymorphisms, few databases provide such information. In particular, most information on CNV availab...
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https://www.riss.kr/link?id=A107670420
2013
-
SCOPUS,SCIE
학술저널
1481-1483(3쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P><B>Summary:</B> Despite a growing interest in a correlation between copy number variations (CNVs) and flanking single nucleotide polymorphisms, few databases provide such information. In particular, most information on CNV availab...
<P><B>Summary:</B> Despite a growing interest in a correlation between copy number variations (CNVs) and flanking single nucleotide polymorphisms, few databases provide such information. In particular, most information on CNV available so far was obtained in Caucasian and Yoruba populations, and little is known about CNV in Asian populations. This article presents a database that provides CNV regions tagged by single nucleotide polymorphisms in about 4700 Koreans, which were detected under strict quality control, manually curated and experimentally validated.</P><P><B>Availability:</B> KGVDB is freely available for non-commercial use at http://biomi.cdc.go.kr/KGVDB.</P><P><B>Contact:</B> kbj6181@cdc.go.kr</P><P><B>Supplementary information:</B> Supplementary data are available at <I>Bioinformatics</I> online.</P>