| Literature DB >> 20671722 |
Anna Paruzynski1, Anne Arens, Richard Gabriel, Cynthia C Bartholomae, Simone Scholz, Wei Wang, Stephan Wolf, Hanno Glimm, Manfred Schmidt, Christof von Kalle.
Abstract
High-throughput integration site profiling has become a feasible tool to assess vector biosafety and to monitor the cell fate of the gene-corrected cell population in clinical gene therapy studies. Here we report a step-by-step protocol for universal genome-wide and comprehensive integrome analysis that can be performed on >10(2)-10(3) samples of interest in parallel. This assay is composed of fast and cost-efficient non-restrictive linear amplification-mediated PCR; optimized sample preparation for pyrosequencing; and automated bioinformatic data mining, including sequence trimming, alignment to the cellular genome and further annotation. Moreover, the workflow of this large-scale assay can be adapted to any PCR-based method aiming to characterize unknown flanking DNA adjacent to a known DNA region. Thus, in combination with next-generation sequencing technologies, large-scale integrome analysis of > 4 x 10(5)-1 x 10(6) integration site sequences can be accomplished within a single week.Mesh:
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Year: 2010 PMID: 20671722 DOI: 10.1038/nprot.2010.87
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491