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.

journal_name

Genomics

journal_title

Genomics

authors

Tully G,Sullivan KM,Nixon P,Stones RE,Gill P

doi

10.1006/geno.1996.0247

subject

Has Abstract

pub_date

1996-05-15 00:00:00

pages

107-13

issue

1

eissn

0888-7543

issn

1089-8646

pii

S0888-7543(96)90247-5

journal_volume

34

pub_type

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