BackgroundDNA sequencing is used ubiquitously: from deciphering genomes[] to determining the primary sequence of small RNAs (smRNAs) [-]. 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 sequences[]. 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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