Bioinformatics Advance Access published online on February 12, 2004
Bioinformatics, doi:10.1093/bioinformatics/bth081
Bioinformatics © Oxford University Press 2004; all rights reserved
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1 Department of Biological Services, the Weizmann Institute of Science, 76100 Rehovot, Israel
* To whom correspondence should be addressed. E-mail: bgumail.bgu.ac.il.
Motivation: High density oligonucleotide arrays are usually annotated in a one-to-one fashion, with each probeset assigned to one gene. However, in reality, subsets of oligonucleotides in a probeset may match sequences within more than one gene, potentially leading to misinterpretations. Moreover, a gene is often represented by more than one probeset, and analyzing probe matches at the mRNA level can help one deduce whether these probesets are derived from the same or different splice variants. Results: The GeneAnnot system comprehensively documents the many-to-many relationships between oligonucleotide array probesets and annotated genes in GeneCardsTM. It performs pairwise alignments between the probe sequences and gene transcripts, and assigns sensitivity and specificity scores to each probeset/gene pair. Availability: http://genecards.weizmann.ac.il/geneannot Supplementary material: GeneAnnot program description and statistics http://genecards.weizmann.ac.il/geneannot/DOC/index.html.
Revised September 2, 2003
Accepted December 19, 2003
Applications note
GeneAnnot: comprehensive two-way linking between oligonucleotide array probesets and GeneCards genes
2 Department of Molecular Genetics, the Weizmann Institute of Science, 76100 Rehovot, Israel
3 Department of Physics of Complex Systems, the Weizmann Institute of Science, 76100 Rehovot, Israel
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