40bp paired reads for novel transcripts identification, which software?

[sqcrft]

Thanks, that is what I am doing now.
I am using the ensembl gtf as reference, also split reads in to 2 piece of 20bp.

other option I am using is to set maximal intron size at 5kb to reduce false discovery due to short 40bp reads. and "--coverage-search"

You can try STAR with --seedSearchStartLmax 20 or smaller (this effectively defines the "segment" length). Even though you are looking for novel transcripts, I would highly recommend "mapping with annotations" as it reduces the misalignment rate.

[alexdobin]

I have some 40bp paired reads RNAseq data, basically that 40 x 2 from each RNA fragment.

It seems to me that, tophat prefers reads that is longer than 25. Is there some software that you recommend and can use such short reads to identify novel transcripts?

Or should I just cut the reads into 3 piece of 13bp long? It seems a little crazy to me. but considering it allow at most 1 junction, then, it seems to me that the method might work?

Any suggestions, fellows?

You can try STAR with --seedSearchStartLmax 20 or smaller (this effectively defines the "segment" length). Even though you are looking for novel transcripts, I would highly recommend "mapping with annotations" as it reduces the misalignment rate.

[sqcrft]

I am now more inclined to use 20 x 2 now. But probably I will try both, computation facility is free for me any way.

I can't find a source now to support the point: 3-piece is better, but I believe I saw it somewhere before.

Here is a not so strong support

"TopHat generates its database of possible splice junctions from two sources of evidence. The first and strongest source of evidence for a splice junction is when two segments from the same read (for reads of at least 45bp) are mapped at a certain distance on the same genomic sequence or when an internal segment fails to map"

http://tophat.cbcb.umd.edu/manual.html#whis

It seems to me that, if you have 3 pieces, you are more likely to have two pieces mapped to two adjacent exons. If you have only two pieces, the only possible way is that, the splicing junction is right in the middle of the read, thus is less likely to happen. But, I couldn't find a formal statement from a paper or the tophat website to support this point.

I don't think tophat necessarily works better with 3 segments for each read, do you see that somewhere? But I know that if your sequences get too short it gets harder to get specific alignments. I would try 2x20 (or try both and compare). There may be other options to change to optimize for shorter reads as well.

[biznatch]

I don't think tophat necessarily works better with 3 segments for each read, do you see that somewhere? But I know that if your sequences get too short it gets harder to get specific alignments. I would try 2x20 (or try both and compare). There may be other options to change to optimize for shorter reads as well.

[sqcrft]

Thanks, I will probably go with cufflinks later.

but that is next step. right now the main issue to me is about the alignment.
The alignment needs to be optimized at the fist place before cufflinks works. It seems to me that 40bp is too short for alignment software optimized for novel transcript identification.

For new transcript detection, try reference-based transcriptome assembly like cufflinks

[sqcrft]

thanks, that is what I am thinking. It seems to me that tophat works better with 3 pieces, that is why they recommend a minimal 75 = 25 x 3 read length.

Now, I am not sure whether I should try cut into 3 pieces or 2 pieces: 13 x 3 or 20 x 2.

[NicoBxl]

For new transcript detection, try reference-based transcriptome assembly like cufflinks

[biznatch]

My understanding of how Tophat works is that if it can't align the entire read it divides it into (by default) 25bp chunks and tries to align those separately. You can change the size they get split into, maybe set it to 20bp so then each of your reads will get split in half.

[sqcrft]

I have some 40bp paired reads RNAseq data, basically that 40 x 2 from each RNA fragment.

It seems to me that, tophat prefers reads that is longer than 25. Is there some software that you recommend and can use such short reads to identify novel transcripts?

Or should I just cut the reads into 3 piece of 13bp long? It seems a little crazy to me. but considering it allow at most 1 junction, then, it seems to me that the method might work?

Any suggestions, fellows?