Library construction and sequencing analysis of 12 mouse eukaryotic transcripts with reference genome

To compare the transcriptomes of the cochlear basilar membrane and cochlear axis in 7d wild-type and knock-in mice, and to explore the molecular mechanism of auditory neuropathy spectrum disorders caused by NELL2 mutations, with the hope of providing experimental bases for the genetic testing of auditory neuropathy spectrum disorders, prenatal diagnosis, and neonatal screening.