RT @mikelove: Got an RNA-seq dataset with 50, 100, 200+ samples? Plug it into a differential expression tool and hope for the best? No! You need to consider QC, EDA, and modeling technical variation, or else risk generating spurious results. A thread on papers, methods, and best practices: https://t.co/p7Zn61QjHw

from Twitter https://twitter.com/danbrewer


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GMail now with IMAP