Why do library concentrations obtained with a qPCR-based method differ from those obtained by other methods?

Why do library concentrations obtained with a qPCR-based method differ from those obtained by other methods?

qPCR only measures the library molecules that can be used for cluster generation. Other methods cannot differentiate between DNA molecules with or without adaptors, resulting in inaccurate quantification of the functional fraction of the library.

General NGS-Seq

related articles