Hi,
I have some Illumina exome data from different runs on NextSeq. I see quite some difference in the number of produced reads per sample, which seems to correlate with the used index.
It occured using different batches of chemicals and I ruled out positional effects in wet lab.
Has anyone run into this problem before?
I have some Illumina exome data from different runs on NextSeq. I see quite some difference in the number of produced reads per sample, which seems to correlate with the used index.
It occured using different batches of chemicals and I ruled out positional effects in wet lab.
Has anyone run into this problem before?
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