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BARCODING
A minimalist barcode can identify a specimen whose DNA is degraded
MEHRDAD HAJIBABAEI*, M. ALEX SMITH*, DANIEL H. JANZEN, JOSEPHINE J. RODRIGUEZ, JAMES B. WHITFIELD and PAUL D. N. HEBERT*
  *Biodiversity Institute of Ontario, Department of Integrative Biology, University of Guelph, Guelph, Ontario, Canada, N1G 2W1   , Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA,   Department of Entomology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA
Correspondence: Mehrdad Hajibabaei, Fax: (519) 767-1656; E-mail: mhajibab@uoguelph.ca
Copyright © 2006 The Authors
Journal compilation © 2006 Blackwell Publishing Ltd
KEYWORDS
COI • DNA barcoding • DNA degradation • fish • Lepidoptera • museum specimens • parasitic wasps • taxonomy

Abstract

AbstractIntroduction
          In silico analysisEmpirical testsDiscussion and conclusionsAcknowledgementsReferences

A DNA barcode based on 650 bp of mitochondrial gene cytochrome c oxidase I is proving to be highly functional in species identification for various animal groups. However, DNA degradation complicates the recovery of a full-length barcode from many museum specimens. Here we explore the use of shorter barcode sequences for identification of such specimens. We recovered short sequences — i.e. ∼100 bp — with a single PCR pass from more than 90% of the specimens in assemblages of moth and wasp museum specimens from which full barcode recovery was only 50%, and the latter were usually less than 8 years old. Short barcodes were effective in identifying specimens, confirming their utility in circumstances where full barcodes are too expensive to obtain and the identification comparisons are within a confined taxonomic group.


Received 3 March 2006; revision received 21 April 2006; accepted 24 May 2006

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1471-8286.2006.01470.x About DOI

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