Hi folks
The new TopHat 1.1.1, nicely handles SOLiD reads, and the results can be piped easily to Cufflinks to make up a RNAseq pipeline. However, the manual page says:
and there are no further guidelines how to tune the parameters if you have shorted reads, as in my case 30bp single-end. Does anybody have any clue on this? Of course this is tunable through editing the TopHat scripts but, the question is how to set the parameters not to screw the whole thing up 
I did a comparison, using TopHat+GTF file and defaults parameters, I get about 5 times less aligned tags than what I get from Bowtie with some sensible parameters.
The new TopHat 1.1.1, nicely handles SOLiD reads, and the results can be piped easily to Cufflinks to make up a RNAseq pipeline. However, the manual page says:
In TopHat 1.1.0, we began supporting Applied Biosystems' Colorspace format. The software is optimized for reads 75bp or longer.

I did a comparison, using TopHat+GTF file and defaults parameters, I get about 5 times less aligned tags than what I get from Bowtie with some sensible parameters.
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