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pubmed-article:16249066pubmed:abstractTextCurrently, challenges exist to acquire long-range (hundreds of kilobase pairs) phase-discriminated sequence across substantial numbers of individuals. We have developed a straightforward method for isolating and characterizing specific genomic regions in a haplospecific manner. Real-time PCR is carried out to STS content map and genotype pools of fosmid clones arrayed in 384-well microtiter plates. Single-nucleotide polymorphisms, microsatellite markers, and insertion-deletion polymorphisms are used to differentiate the target region into haplotype-specific tiling paths. DNA of clones from these tiling paths is retrieved from the library and either sequenced by standard shotgun methods or amplified in vitro and sequenced by a primer-based, directed method. This approach provides convenient access to complete, haplotype-resolved resequencing data from multiple individuals across tens to hundreds of thousands of basepairs. We illustrate its implementation with a detailed example of more than 400 kbp from the human CFTR region, across 15 individuals, and summarize our experience applying it to many other human loci.lld:pubmed
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pubmed-article:16249066pubmed:articleTitleTargeted, haplotype-resolved resequencing of long segments of the human genome.lld:pubmed
pubmed-article:16249066pubmed:affiliationUniversity of Washington Genome Center, Department of Medicine, University of Washington, Seattle, WA 98195, USA.lld:pubmed
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