| Literature DB >> 11058902 |
C Mattocks1, P Tarpey, M Bobrow, J Whittaker.
Abstract
Direct sequencing analysis is largely used to confirm and characterize mutations previously detected by more rapid tests. We have developed a method-Comparative Sequence Analysis (CSA)-that simplifies the analysis of sequencing data facilitating its use as a first screen for mutation detection. Sequence data were split into their component electrophoretograms and the use of a size standard enabled equivalent traces from different individuals to be overlaid. This allowed simple and rapid visual analysis of the results. Using this technique in a blind study, we tested 576 samples for mutations in the Von Hippel-Lindau tumor suppressor gene, VHL. We were able to identify and characterize all 78 known mutations present within the sample set (100% sensitivity and specificity). Copyright 2000 Wiley-Liss, Inc.Entities:
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Year: 2000 PMID: 11058902 DOI: 10.1002/1098-1004(200011)16:5<437::AID-HUMU9>3.0.CO;2-Q
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878