Literature DB >> 8808468

A novel in vivo method to detect DNA sequence variation.

M Faham1, D R Cox.   

Abstract

Mismatch repair detection (MRD) is an in vivo method that uses a change in bacterial colony color to detect DNA sequence variation. DNA fragments to be screened for variation are cloned into two MRD plasmids, and bacteria are transformed with heteroduplexes of these constructs. The resulting colonies are blue in the absence of a mismatch and white in the presence of a mismatch. MRD is capable of detecting a single mismatch in a DNA fragment as large as 10 kb in size. In addition, MRD has the potential for analyzing many fragments simultaneously, offering a powerful method for high-throughput genotyping and mutation detection in a large genomic region.

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Year:  1995        PMID: 8808468     DOI: 10.1101/gr.5.5.474

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  2 in total

1.  Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.

Authors:  K Virtaneva; J Miao; A L Träskelin; N Stone; J A Warrington; J Weissenbach; R M Myers; D R Cox; P Sistonen; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.

Authors:  Peter Brooks; Charles Marcaillou; Maud Vanpeene; Jean-Paul Saraiva; Daniel Stockholm; Stephan Francke; Reyna Favis; Nadine Cohen; Francis Rousseau; Frédéric Tores; Pierre Lindenbaum; Jörg Hager; Anne Philippi
Journal:  BMC Genet       Date:  2009-03-30       Impact factor: 2.797

  2 in total

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