| pubmed-article:17921354 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C1511726 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C0752046 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C1285573 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C2697586 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C0920594 | lld:lifeskim |
| pubmed-article:17921354 | lifeskim:mentions | umls-concept:C1707513 | lld:lifeskim |
| pubmed-article:17921354 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:17921354 | pubmed:dateCreated | 2007-11-2 | lld:pubmed |
| pubmed-article:17921354 | pubmed:abstractText | Comprehensive identification and cataloging of copy number variations (CNVs) is required to provide a complete view of human genetic variation. The resolution of CNV detection in previous experimental designs has been limited to tens or hundreds of kilobases. Here we present PennCNV, a hidden Markov model (HMM) based approach, for kilobase-resolution detection of CNVs from Illumina high-density SNP genotyping data. This algorithm incorporates multiple sources of information, including total signal intensity and allelic intensity ratio at each SNP marker, the distance between neighboring SNPs, the allele frequency of SNPs, and the pedigree information where available. We applied PennCNV to genotyping data generated for 112 HapMap individuals; on average, we detected approximately 27 CNVs for each individual with a median size of approximately 12 kb. Excluding common rearrangements in lymphoblastoid cell lines, the fraction of CNVs in offspring not detected in parents (CNV-NDPs) was 3.3%. Our results demonstrate the feasibility of whole-genome fine-mapping of CNVs via high-density SNP genotyping. | lld:pubmed |
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| pubmed-article:17921354 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17921354 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17921354 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17921354 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17921354 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:17921354 | pubmed:issn | 1088-9051 | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:MoeV GVG | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:BucanMajaM | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:VEGAYY | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:HakonarsonHak... | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:GrantStruan... | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:LiMingyaoM | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:HadleyDexterD | lld:pubmed |
| pubmed-article:17921354 | pubmed:author | pubmed-author:GlessnerJosep... | lld:pubmed |
| pubmed-article:17921354 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17921354 | pubmed:volume | 17 | lld:pubmed |
| pubmed-article:17921354 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17921354 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17921354 | pubmed:pagination | 1665-74 | lld:pubmed |
| pubmed-article:17921354 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:meshHeading | pubmed-meshheading:17921354... | lld:pubmed |
| pubmed-article:17921354 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17921354 | pubmed:articleTitle | PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. | lld:pubmed |
| pubmed-article:17921354 | pubmed:affiliation | Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. | lld:pubmed |
| pubmed-article:17921354 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17921354 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17921354 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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