Assembly of a gene sequence tag microarray by reversible biotin-streptavidin capture for transcript analysis of Arabidopsis thaliana. Wirta, V., Holmberg, A., Lukacs, M., Nilsson, P., Hilson, P., Uhlén, M., Bhalerao, R. P., & Lundeberg, J. BMC Biotechnology, 5(1):5, February, 2005. Paper doi abstract bibtex Transcriptional profiling using microarrays has developed into a key molecular tool for the elucidation of gene function and gene regulation. Microarray platforms based on either oligonucleotides or purified amplification products have been utilised in parallel to produce large amounts of data. Irrespective of platform examined, the availability of genome sequence or a large number of representative expressed sequence tags (ESTs) is, however, a pre-requisite for the design and selection of specific and high-quality microarray probes. This is of great importance for organisms, such as Arabidopsis thaliana, with a high number of duplicated genes, as cross-hybridisation signals between evolutionary related genes cannot be distinguished from true signals unless the probes are carefully designed to be specific.
@article{wirta_assembly_2005,
title = {Assembly of a gene sequence tag microarray by reversible biotin-streptavidin capture for transcript analysis of {Arabidopsis} thaliana},
volume = {5},
issn = {1472-6750},
url = {https://doi.org/10.1186/1472-6750-5-5},
doi = {10.1186/1472-6750-5-5},
abstract = {Transcriptional profiling using microarrays has developed into a key molecular tool for the elucidation of gene function and gene regulation. Microarray platforms based on either oligonucleotides or purified amplification products have been utilised in parallel to produce large amounts of data. Irrespective of platform examined, the availability of genome sequence or a large number of representative expressed sequence tags (ESTs) is, however, a pre-requisite for the design and selection of specific and high-quality microarray probes. This is of great importance for organisms, such as Arabidopsis thaliana, with a high number of duplicated genes, as cross-hybridisation signals between evolutionary related genes cannot be distinguished from true signals unless the probes are carefully designed to be specific.},
number = {1},
urldate = {2021-06-11},
journal = {BMC Biotechnology},
author = {Wirta, Valtteri and Holmberg, Anders and Lukacs, Morten and Nilsson, Peter and Hilson, Pierre and Uhlén, Mathias and Bhalerao, Rishikesh P. and Lundeberg, Joakim},
month = feb,
year = {2005},
keywords = {Additional Data File, Auxin Regulation, Auxin Transporter, Multiple Reuse, Photo Multiplier Tube},
pages = {5},
}
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