Copy Number Variation detection from 1000 Genomes project exon capture sequencing data
Copy Number Variation detection from 1000 Genomes project exon capture sequencing data
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England: BioMed Central Ltd
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English
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England: BioMed Central Ltd
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DNA capture technologies combined with high-throughput sequencing now enable cost-effective, deep-coverage, targeted sequencing of complete exomes. This is well suited for SNP discovery and genotyping. However there has been little attention devoted to Copy Number Variation (CNV) detection from exome capture datasets despite the potentially high im...
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Copy Number Variation detection from 1000 Genomes project exon capture sequencing data
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TN_cdi_doaj_primary_oai_doaj_org_article_e8b134a7cf8045e29d1e8570dc9c1199
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e8b134a7cf8045e29d1e8570dc9c1199
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ISSN
1471-2105
E-ISSN
1471-2105
DOI
10.1186/1471-2105-13-305