Originally posted by Kath
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I've just got exactly the same with my data. What kit did you use for capture?
Cheers
Kath
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so i tried this with a couple of my samples vs human.... i'm getting only 3% not mapping. So there is either very little or no contamination in my sample. So then what can explain the bimodal gc content distro?Originally posted by JackieBadger View Postthis may help http://www.bioinformatics.babraham.a.../fastq_screen/
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i don't know why the image is not being shown in the post... here's the link
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Contamination in my sample?
Hi all!
I just ran a 100bp PE human exome seq run in my lab and was looking at the fastqc results of my run. I am getting this weird pattern in the gc content distribution and was wondering is this normal for an exome run or do i have some sort of contamination? I've run an exome seq before in my lab but saw a distribution which was similar to the theoretical distribution with a shorter peak (yet, still normally distributed). The 2 peaks i'm seeing in the new run is really messing with my head as i have 24 samples all showing the same pattern!
Thanks in advance!Tags: None
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Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
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