MEF & Liver: Gao 2014 Track Settings
 
Ribo-seq unique mappers from from MEF cells and liver tissue which underwent starvation and the corresponding controls (Gao et al. 2014)   (All Elongating Ribosomes (Footprints) tracks)

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     Liver: control  Ribo-seq unique mappers from control liver cells (Gao et al. 2014)   Schema 
     Liver: starvation  Ribo-seq unique mappers from liver cells undergoing amino acid starvation (Gao et al. 2014)   Schema 
     MEF: control  Ribo-seq unique mappers from control MEF cells not undergoing starvation (Gao et al. 2014)   Schema 
     MEF: starvation  Ribo-seq unique mappers from MEF cells undergoing amino acid starvation (Gao et al. 2014)   Schema 

Description

Ribo-seq coverage plots of elongating ribosomes from MEF and mouse liver cells which were deprived of nutrients and their corresponding controls (Gao et al. 2014).

Methods

Raw sequence data were obtained from NCBI GEO database (SRA160745). Data from the following samples were processed:

SRR1630812Ribo-Seq of Liver Cell for Control Mouse
SRR1630813Ribo-Seq of Liver Cell for Fasting Mouse
SRR1630816Ribo-Seq of MEF Cell (Control)
SRR1630817Ribo-Seq of MEF Cell (Amino Acid Starvation)

Adaptor sequences had already been removed from reads. An alignment to ribosomal RNA was then performed using Bowtie, and aligning reads were discarded. An alignment to the mm10 genome assembly was then performed using Bowtie, and these tracks contain the coverage data for uniquely mapping reads from the alignments.

References

Gao, X., Wan, J., Liu, B., Ming, M., Shen, B., Qian, S.B. (2014). Quantitative profiling of initiating ribosomes in vivo. Nat Methods. doi: 10.1038/nmeth.3208