Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server |
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Authors: | H Alexander Ebhardt Kay C Wiese and Peter J Unrau |
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Institution: | (1) Department of Molecular Biology and Biochemistry, Simon Fraser University, 8888 University Drive, V5A 1S6 Burnaby, B.C, Canada;(2) School of Computing Science, Simon Fraser University Surrey, 13450 102nd Ave, V3T 5X3 Surrey, B.C, Canada |
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Abstract: | Background DNA sequencing is used ubiquitously: from deciphering genomes1] to determining the primary sequence of small RNAs (smRNAs) 2–5]. The cloning of smRNAs is currently the most conventional method to determine the actual sequence of these important regulators
of gene expression. Typical smRNA cloning projects involve the sequencing of hundreds to thousands of smRNA clones that are
delimited at their 5' and 3' ends by fixed sequence regions. These primers result from the biochemical protocol used to isolate
and convert the smRNA into clonable PCR products. Recently we completed a smRNA cloning project involving tobacco plants,
where analysis was required for ~700 smRNA sequences6]. Finding no easily accessible research tool to enter and analyze smRNA sequences we developed Ebbie to assist us with our study. |
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