Methods
Data from the following samples were processed:
SRR1630828 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
SRR1630829 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
SRR1630831 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
SRR1630832 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
SRR1630833 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
SRR1630830 | Ribosome coverage data from elongating ribosomes Homo sapiens(Xiangwei, et al. 2014) |
Adapter sequence n was removed from reads using Cutadapt An alignment to ribosomal RNA was performed using Bowtie, and aligning reads were discarded. An alignment to the hg38 genome assembly was performed using Bowtie, and reads below 25 nt were discarded.
These tracks contain the uniquely mapping reads.,ReferencesXiangwei Gao, Ji Wan, Botao Liu, Ming Ma, Ben Shen and Shu-Bing Qian (2014) Quantitative profiling of initiating ribosomes in vivo.doi: 10.1038/nmeth.3208
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