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Old 03-14-2017, 12:26 AM   #1
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Location: Cape Town, South Africa

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Default Reason for POOR per tile sequence quality

We recently performed a sequencing run on the MiSeq sequencer using a V3 (600 cycle kit).

With regards to the per tile quality plot (obtained when using the FastQC analysis software) for one of our samples, it seems as though there is a large area that is flagged in red for R2, indicating that those tiles had worse qualities.

I was just wondering on possible reasons why this would happen and how it could be prevented in future runs?

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Justin87 is offline   Reply With Quote
Old 03-14-2017, 02:59 AM   #2
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Location: Cambridge

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Lightbulb Looks like there is a problem with imaging one of the flowcell surfaces...

It looks like there is a problem with imaging one of the flowcell surfaces...

Either focusing issue (Z axis lens mover in a need of some cleaning/re greasing/calibration) or lots of very small bubbles (if it is an upper surface) (but then they would affect the other surface with such width.

Also check tile thumbnail images, and contact illumina if this instrument is on service contract.

You can also try making movie from thumbnail jpg images using image magic and some scripting...
Markiyan is offline   Reply With Quote
Old 03-14-2017, 05:37 AM   #3
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2xxx tiles are on the bottom surface. I concur with the possibilities raised by Markiyan. Looks like it started somewhere around cycle 35. Definitely a call to tech support is in order.
GW_OK is offline   Reply With Quote

fastqc, per tile quality, troubleshooting

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