Hello everybody,
It's been a while and I'm back with a question.
I am dealing with bacterial RNA-seq data (Illumina, single read, 2 replicates conditions A and B). For convenience, I use Artemis to rapidly visualize RNA-seq coverage. Now, with Artemis, there's an option for SNPs marking, and I observed that some genes are highly variant, i.e. there is a strong concentration of SNPs in one or few regions. When I simply zoom in (until I see my reads as sequences), I can see that some of my reads have a point-mutation here and there but never all of the reads on the same place.
Thank you in advance,
TP
It's been a while and I'm back with a question.
I am dealing with bacterial RNA-seq data (Illumina, single read, 2 replicates conditions A and B). For convenience, I use Artemis to rapidly visualize RNA-seq coverage. Now, with Artemis, there's an option for SNPs marking, and I observed that some genes are highly variant, i.e. there is a strong concentration of SNPs in one or few regions. When I simply zoom in (until I see my reads as sequences), I can see that some of my reads have a point-mutation here and there but never all of the reads on the same place.
- 1 I wonder if these observations of SNPs are genuine or it's only a mere artifact?
- 2 Is there a simple way of calling SNPs genome wide, or even on a specific region (ex. on my gene of interest?)
Thank you in advance,
TP
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