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Old 11-15-2015, 03:59 PM   #1
Pjames
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Location: Australia

Join Date: Nov 2015
Posts: 1
Default Ion Torrent fastqc results

Previously I've used Illumina for my sequencing needs and recently I've been handed some Ion Torrent data to do RNA-Seq.

The fastqc results are significantly poorer than I'm used to. However, I do realise there is considerably different chemistry involved, and fastqc was designed for Illumina, so may not be giving accurate results.

Nevertheless, the large number of failed components is concerning and I was wondering if anyone experienced with Ion Torrent data can tell me if these results mean the samples need to be re-sequenced or not.

summary.png

One of my main concerns, other than quality, is the variable size of the total number of sequences per sample. These vary from 12703948 sequences to 50092930 sequences. Is this normal for Ion Torrent? How can I accurately calculate differential expression with such variable sequences numbers per sample?

Filename 5C_IonXpressRNA_009_rawlib.basecaller.bam
File type Conventional base calls
Encoding Sanger / Illumina 1.9
Total Sequences 17356006
Sequences flagged as poor quality 0
Sequence length 8-352
%GC 48

per_base_sequence.png

per_sequence_gc.png

sequence_duplication.png

kmer.png
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Old 11-16-2015, 11:00 AM   #2
skbrimer
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Your data looks pretty normal for Ion Torrent. I do not use proton data since I'm in the low throughput microbe world. There are a couple of things going on here in your question.

First, your guess about the fastqc values not being equivalent are correct. there is a thread about it here http://seqanswers.com/forums/showthread.php?t=33555 In my experience I have good quality data but my average Q score is in the range of 28-32, it seems to be a "depressed" score. It should be able to show you if your data takes a nose dive however.

Second the different sample sequences has more to due with the library prep then the tech. In general you make your library, normalize to 100uM ea, and then pool from there. If your samples are way out of balance it's most likely to that step either being skipped or just not done with a lot of accuracy.

For your differential analysis question, I'm sorry I'm not sure how to help you. I'm not really doing any of that type of work currently. Also there is a lot of information missing about the experiment to really get into it; however if you are doing whole transcriptome sequencing and each sample's library was prepped the same way wouldn't you be comparing some sort of transformed data? Like sample 1 has 2 fold diff and sample 3 has 4 fold diff with same treatment.
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