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Old 04-11-2011, 03:50 AM   #1
hbt
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Location: UK

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Unhappy Bowtie and Tophat

We are currently trying to analyse Solid RNA-seq data using tophat and/or bowtie.
With default settings tophat is able to align about 35% of reads, whereas bowtie on default is able to align 53%!!
I'm assuming that tophat first runs bowtie then tried to align reads that span exon splice junctions, how is it therefore aligning less reads that bowtie alone!?
With some parameter adjustments (i.e. --best flag) we are able to get up to 70% reads mapped using bowtie alone but in doing this we are not able to map the splice junction reads and the --best flag cannot be set for bowtie when running it through tophat.
Does anyone know if it is possible to get tophat to output only the splice juntion reads (i.e. everything bowtie would not have aligned) so they can be added to the bowtie output, or is there a fairly simple way of altering the bowtie parameters when running it within tophat?

As you might have guessed, I am only just begining my journey into the worderful world of bioinformatics so go easy on me!

Any help or advise would be greatly received!!

Huw
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Old 04-19-2011, 03:13 AM   #2
hlwright
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We also can't understand why tophat is less able to map reads than bowtie despite it using bowtie for the initial mapping?
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Old 04-23-2011, 07:12 PM   #3
adumitri
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Location: Cambridge, MA

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Hi,

Hopefully, this is the right place to post my question:

I ran TopHat v1.2.0 on single reads (40 ntds) generated with Illumina GA IIx. These were the used options:

tophat --max-multihits 2\
--segment-mismatches 2\
--library-type fr-unstranded\
-p 4\
-o sample_tophat_out\
hg19 sample.fastq

After getting the results, I tried to collect some statistics about the runs. Interestingly, in the generated log folder for each of the samples, there are two files that contain statistics data such as:

==> fileq5okX8.log <==
# reads processed: 28183908
# reads with at least one reported alignment: 1081639 (3.84%)
# reads that failed to align: 26764052 (94.96%)
# reads with alignments suppressed due to -m: 338217 (1.20%)
Reported 1219857 alignments to 1 output stream(s)

==> fileueW7Yw.log <==
# reads processed: 28183908
# reads with at least one reported alignment: 20657663 (73.30%)
# reads that failed to align: 3984728 (14.14%)
# reads with alignments suppressed due to -m: 3541517 (12.57%)
Reported 23408344 alignments to 1 output stream(s)

There is no documentation on TopHat's website on what these two files actually represent. As you can see, the summaries look pretty different - I am not sure why there are two files in the first place, nor do I understand why there is such a large difference between the % of aligned reads.

There are also two additional files that seem to contain relevant data: reports.log and prep_reads.log. Does anyone know what the results presented in all these files are?

Thank you so much!
Alexandra
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Old 04-24-2011, 09:02 AM   #4
ttnguyen
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Looks like the files in log folder are not much informative. It is quite easy to collect statistics about the mapping by looking at 'accepted_hits.bam'.
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Old 01-12-2012, 07:42 AM   #5
sterding
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This post helps a lot to the question here:

http://biostar.stackexchange.com/que...ings-in-tophat
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