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Microcoding:: the second step in DNA barcoding

delete2005-09-14
delete109
delete
OA
AI
R
Richard C. Summerbell
C
C. André Lévesque
K
Keith A. Seifert
M
Marjan Bovers
J
Jack W. Fell
D
Diaz, MR
T
T. Boekhout
D
de Hoog, GS
J
Joost A. Stalpers
P
P.W. Crous
DOI:10.1098/rstb.2005.1721delete
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Abstract

Abstract

En 中文
After the process of DNA barcoding has become well advanced in a group of organisms, as it has in the economically important fungi, the question then arises as to whether shorter and literally more barcode-like DNA segments should be utilized to facilitate rapid identification and, where applicable, detection. Through appropriate software analysis of typical full-length barcodes (generally over 500 base pairs long), uniquely distinctive oligonucleotide 'microcodes' of less than 25 bp can be found that allow rapid identification of circa 100-200 species on various array-like platforms. Microarrays can in principle fulfill the function of microcode-based species identification but, because of their high cost and low level of reusability, they tend to be less cost-effective. Two alternative platforms in current use in fungal identification are reusable nylon-based macroarrays and the Luminex system of specific, colour-coded DNA detection beads analysed by means of a flow cytometer. When the most efficient means of rapid barcode-based species identification is sought, a choice can be made either for one of these methodologies or for basic high-throughput sequencing, depending on the strategic outlook of the investigator and on current costs. Arrays and functionally similar platforms may have a particular advantage when a biologically complex material such as soil or a human respiratory secretion sample is analysed to give a census of relevant species present.
Keywords:
macroarrays
species identification
barcoding
fungi
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Journal

Philosophical Transactions of the Royal Society B-Biological Sciences cover
Philosophical Transactions of the Royal Society B-Biological Sciences
IF:
4.7
Papers:
8.7K
Citations:
5.6W

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