Hi all,
I have a particular sample where it seems the base calling on the MiSeq has failed. Very few reads pass filter, and those that do contain mostly C base calls. I have sequenced similar samples before on the HiSeq, the base composition is closer to 50% GC.
When we look at the pictures of the flowcell it looks like all four bases are represented and the skew toward C is not so great as the basecalling would lead us to believe. Illumina tech support tells us that this is a problem with the sample.
Since visually it seems that the sample might be ok and that this is a problem with Illumina's base caller, I would like to attempt base calling with a different algorithm. NaiveBayesCall for example doesn't require phiX training data, however I would need to get the cluster intensity (.cif) files to use it.
Does anybody know if it's possible to get the .cif files from a MiSeq run? Can the instrument be programmed to save these somewhere before a run starts?
I have a particular sample where it seems the base calling on the MiSeq has failed. Very few reads pass filter, and those that do contain mostly C base calls. I have sequenced similar samples before on the HiSeq, the base composition is closer to 50% GC.
When we look at the pictures of the flowcell it looks like all four bases are represented and the skew toward C is not so great as the basecalling would lead us to believe. Illumina tech support tells us that this is a problem with the sample.
Since visually it seems that the sample might be ok and that this is a problem with Illumina's base caller, I would like to attempt base calling with a different algorithm. NaiveBayesCall for example doesn't require phiX training data, however I would need to get the cluster intensity (.cif) files to use it.
Does anybody know if it's possible to get the .cif files from a MiSeq run? Can the instrument be programmed to save these somewhere before a run starts?
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