Hi there,
I believe many people in Illumina NGS community use qPCR as a quality check for the libraries before taking them for the sequencing. Im curious to know if any1 here uses BA (Bionalyzer) profile as a quality parameter. If yes, I wll be very happy to know how do u estimate the # of picomoles using BA profile as a criteria and hw good is the output of it?
I believe many people in Illumina NGS community use qPCR as a quality check for the libraries before taking them for the sequencing. Im curious to know if any1 here uses BA (Bionalyzer) profile as a quality parameter. If yes, I wll be very happy to know how do u estimate the # of picomoles using BA profile as a criteria and hw good is the output of it?
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