The origin of the samples and the ribosome-footprint methodology are described in the article by Bifeld et al., 2018 (PMID: 30505948). Raw sequencing reads (Illumina single-end reads in FASTQ format)
The features described are: number of clone; fold change (F ≥ 1.7, up-regulation; F ≤ -1.7, down-regulation); log2F and standard deviation (SD); Student's t-test, p; multiple sequence alignment expect
