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Math is not my strong point! I've pooled 12 samples, previously quantified by KAPA quant, based on their size-adjusted concentration. My library peaks average 700 bp. The KAPA quant of the pooled, size-adjusted library is less than I expected (not super low, just a bit lower than I was aiming for). Was the problem just pipetting or should I have pooled based on the non-adjusted concentration? I'm not sure that I haven't adjusted for size twice, and I don't want to overload the MiSeq.
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The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...05-06-2024, 07:48 AM -
The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...04-22-2024, 07:01 AM