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#1 |
Junior Member
Location: Nottingham Join Date: Nov 2015
Posts: 6
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Hi
I have some FastQC results I have generated from Illumina 16s sequences. I have attached an example of the results for one of the demultiplexed fastq files, but they all look simillar. I think that the per base quality score looks ok but I am not sure about the other statistics. I have only worked with WGS data before and I haven't been able to find any information on if these are normal. Any information/links to resources on if these look ok would be really helpful. Thanks Michelle |
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#2 |
Senior Member
Location: uk Join Date: Mar 2009
Posts: 667
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I think they look OK. The thing with 16S reads is that they are amplicons, and that all the
sequences are very similar. I had seen a document on the website of an Italian company named IGATech some months ago, which showed typical FastQC plots for 16S data, and improved plots with their method, which I think involved some type of heterogeneity spacers, but I can't find it now. https://igatechnology.com Last edited by mastal; 05-22-2018 at 04:04 PM. |
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#3 |
Junior Member
Location: Nottingham Join Date: Nov 2015
Posts: 6
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Hi Mastal
Thanks for the reply. I thought that might be the case, I'm just trying to understand the data better. I managed to find a bit of a tutorial about this too. https://monsterbashseq.wordpress.com...ality-control/ |
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Tags |
16s, fastqc, metagenomics, quality check |
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