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Thread | Thread Starter | Forum | Replies | Last Post |
FastQC,kmer content, per base sequence content: is this good enough | mgg | Bioinformatics | 10 | 11-06-2013 11:45 PM |
FastQC: 3' bias (weird peaks) in Kmer content graphics | Ann7 | RNA Sequencing | 2 | 06-19-2013 06:31 AM |
FastQC Kmer content: spike in reverse read | reubennowell | Bioinformatics | 4 | 06-12-2013 03:56 AM |
FastQC: odd kmer content | zshuhua | Introductions | 3 | 05-13-2013 08:36 PM |
kmer content warning in FastQC | vallejov | RNA Sequencing | 0 | 04-05-2013 11:10 AM |
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#1 |
Junior Member
Location: Mexico Join Date: Aug 2013
Posts: 1
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Hello,
I have 4 different samples and in all of them I got some weird peaks along the sequences in FastQC kmer content graphics (plz see the attached graphs). I would appreciate it very much if anyone has a clue of what is happened in my data set. Many thanks! |
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#2 |
Member
Location: US Join Date: Sep 2010
Posts: 14
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What type of samples are these(whole genome, transcriptome, RAD, etc.)? It could be contamination of some sort. You can tile the kmers together to get a longer sequence (TATCCTCCAGTG). I would compare that sequence to your adapters, primers, and other possible sources of contamination. I would also check and see how many reads this is actually affecting.
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