A gene-specific DNA sequencing chip for exploring molecular evolutionary change.

Abstract:

:Sequencing by hybridization (SBH) approaches to DNA sequencing face two conflicting constraints. First, in order to ensure that the target DNA binds reliably, the oligonucleotide probes that are attached to the chip array must be >15 bp in length. Secondly, the total number of possible 15 bp oligonucleotides is too large (>4(15)) to fit on a chip with current technology. To circumvent the conflict between these two opposing constraints, we present a novel gene-specific DNA chip design. Our design is based on the idea that not all conceivable oligonucleotides need to be placed on a chip--only those that capture sequence combinations occurring in nature. Our approach uses a training set of aligned sequences that code for the gene in question. We compute the minimum number of oligonucleotides (generally 15-30 bp in length) that need to be placed on a DNA chip to capture the variation implied by the training set using a graph search algorithm. We tested the approach in silico using cytochrome-b sequences. Results indicate that on average, 98% of the sequence of an unknown target can be determined using the approach.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Fedrigo O,Naylor G

doi

10.1093/nar/gkh210

keywords:

subject

Has Abstract

pub_date

2004-02-18 00:00:00

pages

1208-13

issue

3

eissn

0305-1048

issn

1362-4962

pii

32/3/1208

journal_volume

32

pub_type

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