Expressed sequence tags (ESTs) offer a rapid and cost effective method to understand the transcriptome of an organism, leading to enormous data as short, unedited, single-pass sequence reads. Several computational methods are essential to assemble and annotate them. A comprehensive workflow approach resulting in gene and protein annotation is as yet unavailable [1].
We have compared currently available methods adopted for each step of EST analysis including EST clustering, assembly, consensus generation and tools for DNA or protein downstream annotation, on benchmark EST datasets [1]. We have incorporated the best combination of programs while designing ESTExplorer [2].
Please cite the following references if you use ESTExplorer:
1. Nagaraj SH, Gasser RB, Ranganathan S. A hitchhiker's guide to expressed sequence tag (EST) analysis. Brief Bioinform, 2007, 8, 6-21;
2. Nagaraj SH, Deshpande N,Gasser RB, Ranganathan S. ESTExplorer: an automated assembly and annotation platform to analyse expressed
sequence tags (ESTs).Nucleic Acids Res. 2007 Jul;35
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08/08/2010 : We have upgraded our system and ESTExplorer is back online again!!
23/03/2007 : New smat files from five organisms have been added to conceptual translation in Phase III of ESTExplorer.
20/03/2007 : ESTs can be now be assembled using quality files. If quality values are available, we have provided an expert option, so that users can upload this information as *.qual file for CAP3 program.
18/03/2007 : New organisms (Oryza sativa, Danio rerio, Gallus gallus, Drosophila melanogaster and Canis familiaris) have been added to conceptual translation (Phase III) of ESTExplorer.
20/02/2007 : We are in the process of doubling our computational resources to enable speedy processing of all the programs in ESTExplorer.