We are analyzing illumina 75bp paired-end RNA-seq data. For mapping, what are the key differences between TopHat and Illumina's eland-CASAVA pipeline for RNA-seq data?
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Hi kopi-o,Originally posted by kopi-o View PostThe Illumina pipeline will only look for known splice junctions, while TopHat can (at least in theory) find novel splice junctions.
Thanks for highlighting that difference.
One other difference could be the no. of basepairs that the algorithm expects as the 'seed' in order to generate accurate alignments. For illumina-eland, I know it is 32bp, but not sure what seed length does TopHat expect.
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Hi kopi-o,
Thanks for highlighting the difference on splice junction prediction between Illumina-Eland and TopHat.
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