FastQC, v0.11.5, error: Too many tiles ...

[echo manolis]

Ubuntu

Hi,

I have FastQC, v0.11.5 and I want to evaluate an Illumina run (pairend). I have reads of 150bp and a average coverage near to 60X.

When I run FastQC after some time I have this kind of error:

"Too many tiles (>500) so giving up trying to do per-tile qualities since we're probably parsing the file wrongly"

I tried to increase the threads with "-t 10" but I still have the same error.

What I have to do to fix this error?

Best,
echo manolis

[GenoMax]

If this is NovaSeq data then you should upgrade to the latest FastQC (v. 0.11.7).

[echo manolis]

ok thanks. I will try and I will let you know!

Best