Annotating nonspecific SAGE tags with microarray data.

@article{citeulike:1969803, abstract = {SAGE (serial analysis of gene expression) detects transcripts by extracting short tags from the transcripts. Because of the limited length, many SAGE tags are shared by transcripts from different genes. Relying on sequence information in the general gene expression database has limited power to solve this problem due to the highly heterogeneous nature of the deposited sequences. Considering that the complexity of gene expression at a single tissue level should be much simpler than that in the general expression database, we reasoned that by restricting gene expression to tissue level, the accuracy of gene annotation for the nonspecific SAGE tags should be significantly improved. To test the idea, we developed a tissue-specific SAGE annotation database based on microarray data (). This database contains microarray expression information represented as UniGene clusters for 73 normal human tissues and 18 cancer tissues and cell lines. The nonspecific SAGE tag is first matched to the database by the same tissue type used by both SAGE and microarray analysis; then the multiple UniGene clusters assigned to the nonspecific SAGE tag are searched in the database under the matched tissue type. The UniGene cluster presented solely or at higher expression levels in the database is annotated to represent the specific gene for the nonspecific SAGE tags. The accuracy of gene annotation by this database was largely confirmed by experimental data. Our study shows that microarray data provide a useful source for annotating the nonspecific SAGE tags.}, address = {Center for Functional Genomics, ENH Research Institute, Northwestern University, Chicago, IL 60611, USA.}, author = {Ge, X. and Jung, Y. C. and Wu, Q. and Kibbe, W. A. and Wang, S. M. }, citeulike-article-id = {1969803}, doi = {10.1016/j.ygeno.2005.08.014}, issn = {0888-7543}, journal = {Genomics}, month = {January}, number = {1}, pages = {173--180}, posted-at = {2007-11-24 03:36:53}, priority = {2}, title = {Annotating nonspecific SAGE tags with microarray data.}, url = {http://dx.doi.org/10.1016/j.ygeno.2005.08.014}, volume = {87}, year = {2006} }

TY - JOUR ID - citeulike:1969803 L3 - citeulike-article-id:1969803 TI - Annotating nonspecific SAGE tags with microarray data. JF - Genomics VL - 87 IS - 1 SP - 173 EP - 180 AD - Center for Functional Genomics, ENH Research Institute, Northwestern University, Chicago, IL 60611, USA. SN - 0888-7543 N2 - SAGE (serial analysis of gene expression) detects transcripts by extracting short tags from the transcripts. Because of the limited length, many SAGE tags are shared by transcripts from different genes. Relying on sequence information in the general gene expression database has limited power to solve this problem due to the highly heterogeneous nature of the deposited sequences. Considering that the complexity of gene expression at a single tissue level should be much simpler than that in the general expression database, we reasoned that by restricting gene expression to tissue level, the accuracy of gene annotation for the nonspecific SAGE tags should be significantly improved. To test the idea, we developed a tissue-specific SAGE annotation database based on microarray data (). This database contains microarray expression information represented as UniGene clusters for 73 normal human tissues and 18 cancer tissues and cell lines. The nonspecific SAGE tag is first matched to the database by the same tissue type used by both SAGE and microarray analysis; then the multiple UniGene clusters assigned to the nonspecific SAGE tag are searched in the database under the matched tissue type. The UniGene cluster presented solely or at higher expression levels in the database is annotated to represent the specific gene for the nonspecific SAGE tags. The accuracy of gene annotation by this database was largely confirmed by experimental data. Our study shows that microarray data provide a useful source for annotating the nonspecific SAGE tags. AU - Ge, X AU - Jung, YC AU - Wu, Q AU - Kibbe, WA AU - Wang, SM PY - 2006/01// UR - http://dx.doi.org/10.1016/j.ygeno.2005.08.014 ER -