Skip Navigation



Bioinformatics Advance Access published online on July 27, 2007

Bioinformatics, doi:10.1093/bioinformatics/btm360
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
23/18/2385    most recent
btm360v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Liu, H.
Right arrow Articles by Weinstein, J. N
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Liu, H.
Right arrow Articles by Weinstein, J. N
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author (2007). Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

AffyProbeMiner: a web resource for computing or retrieving accurately redefined Affymetrix probe sets

Hongfang Liu 1,2,$, Barry R Zeeberg 1,$, Qu Gang 3, A Gunes Koru 4, Alessandro Ferrucci 1,5, Ari Kahn 1,6, Michael C Ryan 6, Antej Nuhanovic 7,8, Peter J Munson 7, William C Reinhold 1, David W Kane 8 and John N Weinstein 1

1Genomics and Bioinformatics Group, Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA
2Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, 4000 Reservoir Road, NW, Washington, DC 20007, USA
3Department of Electrical and Computer Engineering, University of Maryland, College Park, College Park, MD 20742, USA
4Department of Information Systems, University of Maryland, Baltimore County, 1000 Hilltop Circle, MD 21050, USA
5Department of Computer Science and Electrical Engineering, University of Maryland, Baltimore County, 1000 Hilltop Circle, MD 21050, USA
6Department of Bioinformatics, George Mason University, Fairfax, Virginia, 20110, USA
7Mathematical and Statistical Computing Laboratory, Division of Computational Bioscience, Center for Information Technology, National Institutes of Health, Bethesda, MD 20892, USA
8SRA International, 4300 Fair Lakes Court, Fairfax, VA 22033, USA

To whom correspondence should be addressed. Prof. Hongfang Liu, E-mail: hl224{at}georgetown.edu


   Abstract

Motivation: Affymetrix microarrays are widely used to measure global expression of mRNA transcripts. That technology is based on the concept of a probe set. Individual probes within a probe set were originally designated by Affymetrix to hybridize with the same unique mRNA transcript. Because of increasing accuracy in knowledge of genomic sequences, however, a substantial number of the manufacturer's original probe groupings and mappings are now known to be inaccurate and must be corrected. Otherwise, analysis and interpretation of an Affymetrix microarray experiment will be in error.

Results: AffyProbeMiner is a computationally-efficient platform-independent tool that uses all RefSeqs and validated complete coding sequences in GenBank to (1) regroup the individual probes into consistent probe sets and (2) remap the probe sets to the correct sets of mRNA transcripts. The individual probes are grouped into probe sets that are ‘transcript-consistent’ in that they hybridize to the same mRNA transcript (or transcripts) and, therefore, measure the same entity (or entities). About 65.6% of the probe sets on the HG-U133A chip were affected by the remapping. Pre-computed regrouped and remapped probe sets for many Affymetrix microarrays are made freely available at the AffyProbeMiner web site. Alternatively, we provide a web service that enables the user to perform the remapping for any type of short-oligo commercial or custom array that has an Affymetrix-format Chip Definition File (CDF). Important features that differentiate AffyProbeMiner from other approaches are flexibility in the handling of splice variants, computational efficiency, extensibility, customizability, and user-friendliness of the interface.

Availability: The web interface and software (GPL open source license), are publicly-accessible at http://discover.nci.nih.gov/affyprobeminer.

Contact: hl224{at}georgetown.edu or barry{at}discover.nci.nih.gov

Associate Editor: Dr. Joaquin Dopazo

$ Contributed equally


Received on February 1, 2007; revised on June 20, 2007; accepted on July 9, 2007

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
J. Boros, A. O'Donnell, I. J. Donaldson, A. Kasza, L. Zeef, and A. D. Sharrocks
Overlapping promoter targeting by Elk-1 and other divergent ETS-domain transcription factor family members
Nucleic Acids Res., September 29, 2009; (2009) gkp804v1.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
D. G. Morris, S. M. Waters, S. D. McCarthy, J. Patton, B. Earley, R. Fitzpatrick, J. J. Murphy, M. G. Diskin, D. A. Kenny, A. Brass, et al.
Pleiotropic effects of negative energy balance in the postpartum dairy cow on splenic gene expression: repercussions for innate and adaptive immunity
Physiol Genomics, September 1, 2009; 39(1): 28 - 37.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
F. E. Nicolas, H. Pais, F. Schwach, M. Lindow, S. Kauppinen, V. Moulton, and T. Dalmay
Experimental identification of microRNA-140 targets by silencing and overexpressing miR-140
RNA, December 1, 2008; 14(12): 2513 - 2520.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.