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Library preparation, RNA sequencing, and differential expression analysis We generated libraries from participants with DM1 and DMD ( N = 4 each group) using 10 ng urine exRNA from each sample and the Takara SMARTer Stranded Total RNA Sequencing kit V2pico input mammalian (Takara product number 634412)

doi: 10.1007/s43440-022-00390-z 128 SoniD.UpadhayayS.DhurejaM.ArthurR.KumarP

Moreover, little information is available on GA in clinical research, so we can undertake in-depth studies to develop a more reliable basis for GAs future application in clinical applications

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