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Comprehensive assessment of sequence variation within the copy number variable defensin cluster on 8p23 by target enriched in-depth 454 sequencing

BACKGROUND: In highly copy number variable (CNV) regions such as the human defensin gene locus, comprehensive assessment of sequence variations is challenging. PCR approaches are practically restricted to tiny fractions, and next-generation sequencing (NGS) approaches of whole individual genomes e.g...

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Bibliografiska uppgifter
Huvudupphovsmän: Taudien, Stefan, Szafranski, Karol, Felder, Marius, Groth, Marco, Huse, Klaus, Raffaelli, Francesca, Petzold, Andreas, Zhang, Xinmin, Rosenstiel, Philip, Hampe, Jochen, Schreiber, Stefan, Platzer, Matthias
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2011
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Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3118217/
https://ncbi.nlm.nih.gov/pubmed/21592371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-12-243
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