Supplemental Material for Ma et al., 2019
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The Neurospora crassa wild type strans were growthed in minimal
slants for two weeks and cultivated in 2% glucose media under DD condition. The
strain was cultured under dark for 12h and 20h. And RNA
libraries were prepared for sequencing using standard Illumina protocols after
total RNA was extracted. Then RNA-seq was performed. Differential
expression analysis of two samples was performed using the previous statistics
model. The resulting P-values were adjusted using the Benjamini and Hochberg’s
approach for controlling the false discovery rate and adjusted P-value <0.05
were assigned as differentially expressed gene.
提供机构：
GSA Journals
创建时间：
2019-09-10
