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Hi everyone
We've had a problem with a sequencing run and I would like to ask for a re-run with justification.
We submitted 4 libraries to size-select via pippin prep, pool and run SE 150 on a MiSeq. The pippin prep was to select between 200-600bp fragments, and apparently worked well (image of one of the libraries attached, the others looked the same).
The run came back and it's pretty obvious that something went wrong. between 70-80% of the reads are primer dimers, sized 135bp. I'm attaching the FastQC per-base quality. The first 6bp were in-line barcode. After that there is a big drop in quality at the 77bp mark, which is the end of the primer dimer fragment. However, the fragments keep giving base calls, albeit at very poor quality. Is this what the software does when the reads go beyond the end of the fragment?
The discrepancy between the reads and the bioanalyzer profile post-pippinprep makes me think that they messed up and loaded the pre-pippinprep sample into the flow cell. But I can also imagine that the bioanalyzer could give a wrong size profile in some conditions, or that there could be some primer dimer contamination that would not be visible on bioanalyzer.
Does anyone have experience in this kind of problem? Should the read lengths from the MiSeq run be concordant with the bioanalyzer profile, or is that too much to ask?
Thank you in advance!
We've had a problem with a sequencing run and I would like to ask for a re-run with justification.
We submitted 4 libraries to size-select via pippin prep, pool and run SE 150 on a MiSeq. The pippin prep was to select between 200-600bp fragments, and apparently worked well (image of one of the libraries attached, the others looked the same).
The run came back and it's pretty obvious that something went wrong. between 70-80% of the reads are primer dimers, sized 135bp. I'm attaching the FastQC per-base quality. The first 6bp were in-line barcode. After that there is a big drop in quality at the 77bp mark, which is the end of the primer dimer fragment. However, the fragments keep giving base calls, albeit at very poor quality. Is this what the software does when the reads go beyond the end of the fragment?
The discrepancy between the reads and the bioanalyzer profile post-pippinprep makes me think that they messed up and loaded the pre-pippinprep sample into the flow cell. But I can also imagine that the bioanalyzer could give a wrong size profile in some conditions, or that there could be some primer dimer contamination that would not be visible on bioanalyzer.
Does anyone have experience in this kind of problem? Should the read lengths from the MiSeq run be concordant with the bioanalyzer profile, or is that too much to ask?
Thank you in advance!
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