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pmid:18598341

Strong position-dependent effects of sequence mismatches on signal ratios measured using long oligonucleotide microarrays.

Catriona Rennie · Harry A Noyes · Stephen J Kemp · Helen Hulme · Andy Brass · David C Hoyle

BMC genomics · 2008 doi:10.1186/1471-2164-9-317

Paper

complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Strong position-dependent effects of sequence mismatches on signal ratios measured using long oligonucleotide microarrays.
doi
10.1186/1471-2164-9-317
pmid
18598341
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Catriona Rennie
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Harry A Noyes
[2]
Stephen J Kemp
[3]
Helen Hulme
[4]
Andy Brass
[5]
David C Hoyle
journal
BMC genomics
year
2008
abstract
BACKGROUND: Microarrays are an important and widely used tool. Applications include capturing genomic DNA for high-throughput sequencing in addition to the traditional monitoring of gene expression and identifying DNA copy number variations. Sequence mismatches between probe and target strands are known to affect the stability of the probe-target duplex, and hence the strength of the observed signals from microarrays. RESULTS: We describe a large-scale investigation of microarray hybridisations to murine probes with known sequence mismatches, demonstrating that the effect of mismatches is strongly position-dependent and for small numbers of sequence mismatches is correlated with the maximum length of perfectly matched probe-target duplex. Length of perfect match explained 43% of the variance in log2 signal ratios between probes with one and two mismatches. The correlation with maximum length of perfect match does not conform to expectations based on considering the effect of mismatches purely in terms of reducing the binding energy. However, it can be explained qualitatively by considering the entropic contribution to duplex stability from configurations of differing perfect match length. CONCLUSION: The results of this study have implications in terms of array design and analysis. They highlight the significant effect that short sequence mismatches can have upon microarray hybridisation intensities even for long oligonucleotide probes. All microarray data presented in this study are available from the GEO database 1, under accession number [GEO: GSE9669]
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To compare the effect of the type of substitution to the effect of the position of the mismatch, we performed a two-way ANOVA of log2 signal ratios from the whole genome array data, with type of substitution and distance of mismatch from the probe end as explanatory factors.
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To compare the effect of the type of substitution to the effect of the position of the mismatch, we performed a two-way ANOVA of log2 signal ratios from the whole genome array data, with type of substitution and distance of mismatch from the probe end as explanatory factors.
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129, AJ and Balb CGH against C57 reference on Agilent whole genome and custom mouse long oligonucleotide arrays
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Complete file
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