Alternative mapping of probes to genes for <it>Affymetrix </it>chips

<p>Abstract</p> <p>Background</p> <p>Short oligonucleotide arrays have several probes measuring the expression level of each target transcript. Therefore the selection of probes is a key component for the quality of measurements. However, once probes have been selected...

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Main Authors: Friis-Hansen Lennart, Møller Morten, Gautier Laurent, Knudsen Steen
Format: Article
Language:English
Published: BMC 2004-08-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/5/111
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spelling doaj-85b324d250f449fa8aed5e07436c178b2020-11-24T20:51:42ZengBMCBMC Bioinformatics1471-21052004-08-015111110.1186/1471-2105-5-111Alternative mapping of probes to genes for <it>Affymetrix </it>chipsFriis-Hansen LennartMøller MortenGautier LaurentKnudsen Steen<p>Abstract</p> <p>Background</p> <p>Short oligonucleotide arrays have several probes measuring the expression level of each target transcript. Therefore the selection of probes is a key component for the quality of measurements. However, once probes have been selected and synthesized on an array, it is still possible to re-evaluate the results using an updated mapping of probes to genes, taking into account the latest biological knowledge available.</p> <p>Methods</p> <p>We investigated how probes found on recent commercial microarrays for human genes (Affymetrix HG-U133A) were matching a recent curated collection of human transcripts: the NCBI RefSeq database. We also built mappings and used them in place of the original probe to genes associations provided by the manufacturer of the arrays.</p> <p>Results</p> <p>In a large number of cases, 36%, the probes matching a reference sequence were consistent with the grouping of probes by the manufacturer of the chips. For the remaining cases there were discrepancies and we show how that can affect the analysis of data.</p> <p>Conclusions</p> <p>While the probes on Affymetrix arrays remain the same for several years, the biological knowledge concerning the genomic sequences evolves rapidly. Using up-to-date knowledge can apparently change the outcome of an analysis.</p> http://www.biomedcentral.com/1471-2105/5/111
collection DOAJ
language English
format Article
sources DOAJ
author Friis-Hansen Lennart
Møller Morten
Gautier Laurent
Knudsen Steen
spellingShingle Friis-Hansen Lennart
Møller Morten
Gautier Laurent
Knudsen Steen
Alternative mapping of probes to genes for <it>Affymetrix </it>chips
BMC Bioinformatics
author_facet Friis-Hansen Lennart
Møller Morten
Gautier Laurent
Knudsen Steen
author_sort Friis-Hansen Lennart
title Alternative mapping of probes to genes for <it>Affymetrix </it>chips
title_short Alternative mapping of probes to genes for <it>Affymetrix </it>chips
title_full Alternative mapping of probes to genes for <it>Affymetrix </it>chips
title_fullStr Alternative mapping of probes to genes for <it>Affymetrix </it>chips
title_full_unstemmed Alternative mapping of probes to genes for <it>Affymetrix </it>chips
title_sort alternative mapping of probes to genes for <it>affymetrix </it>chips
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2004-08-01
description <p>Abstract</p> <p>Background</p> <p>Short oligonucleotide arrays have several probes measuring the expression level of each target transcript. Therefore the selection of probes is a key component for the quality of measurements. However, once probes have been selected and synthesized on an array, it is still possible to re-evaluate the results using an updated mapping of probes to genes, taking into account the latest biological knowledge available.</p> <p>Methods</p> <p>We investigated how probes found on recent commercial microarrays for human genes (Affymetrix HG-U133A) were matching a recent curated collection of human transcripts: the NCBI RefSeq database. We also built mappings and used them in place of the original probe to genes associations provided by the manufacturer of the arrays.</p> <p>Results</p> <p>In a large number of cases, 36%, the probes matching a reference sequence were consistent with the grouping of probes by the manufacturer of the chips. For the remaining cases there were discrepancies and we show how that can affect the analysis of data.</p> <p>Conclusions</p> <p>While the probes on Affymetrix arrays remain the same for several years, the biological knowledge concerning the genomic sequences evolves rapidly. Using up-to-date knowledge can apparently change the outcome of an analysis.</p>
url http://www.biomedcentral.com/1471-2105/5/111
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