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Bioinformatics Service Report

IMMAGINA Biotechnology S.r.l.

04/03/2024

Thank you for choosing IMMAGINA Biotechnology for your analysis needs! This interactive report provides a comprehensive overview of your results, with easy-to-read graphs and charts that bring your data to life.

If you have any questions about the analyses, please don’t hesitate to contact us at

Workflow

1. Summary Table

Table 1:

Summary of sample names and groups used to Calculate Translation Efficency (TE)

2. Principal component analysis (PCA)

PCA Riboseq

This plot shows the Principal component analysis (PCA) of Ribo-Seq experiment. The PCA plot shows the data points projected onto the first two principal components, which are the two new axes that account for the most variance in the data.

PCA RNAseq

This plot shows the Principal component analysis (PCA) of RNAseq experiment. The PCA plot shows the data points projected onto the first two principal components, which are the two new axes that account for the most variance in the data.

3. Translation Efficency (TE) volcano plot and Directional plot

TE volcano plot

The Translation Efficency (TE) volcano plot shows the distribution of gene based on their log2FoldChange in TE and their p-value. TE = log2(Condition_1(RPF/mRNA) / Condition_2(RPF/mRNA))

Directional plot

The ‘Directional plot’ shows the log2 fold change in Ribo-seq (x-axis) versus the log2 fold change in RNA-seq (y-axis) for each gene. The four dashed lines indicate log2 fold change values of -1 or +1. ‘Homodirectional’ genes have increased or decreased reads in both Ribo-seq and RNA-seq relative to the control (log2 fold change). ‘Crossdirectional’ genes have increased reads in Ribo-seq or RNA-seq relative to the control, but decreased reads in the other assay.

4. Outputs

* Raw Data
* BAM files
* Counts for each RNAseq and Riboseq sample
* TE pvalue and log2FC
* Plots