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PubMed · 8661030

Rapid detection of mitochondrial sequence polymorphisms using multiplex solid-phase fluorescent minisequencing.

Abstract

This work describes a novel method, multiplex solid-phase fluorescent minisequencing, for the simultaneous detection of several point mutations and/or small deletions and insertions. The method is applied to the analysis of mitochondrial DNA polymorphisms for the purposes of individual identification. A database of 152 British Caucasians and 103 British Afro-Caribbeans has been constructed, and the probability of a chance match between two unrelated individuals is calculated as 0.054 for Caucasians and 0.026 for Afro-Caribbeans.

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BibTeXRIS

G Tully, K M Sullivan, P Nixon, R E Stones, P Gill. 1996-05-15. Rapid detection of mitochondrial sequence polymorphisms using multiplex solid-phase fluorescent minisequencing.. https://doi.org/10.1006/geno.1996.0247

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