Last updated: 2019-09-16

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Knit directory: cheRNA_pilot/analysis/

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Rmd de62ab7 Benjmain Fair 2019-08-13 Start workflowr project.

Here I will analyze chromatin associated RNA-seq datasets for 5 LCL lines, prepped by Staley lab. Alongside these new dataests, I will also look at some published datasets for the same lines for RNA-seq ,4sU-RNA-seq (30min, 60min), as well as the chromatin associated RNA and soluble nuclear RNA from Werner et al, and some RNA-seq datasets using different fractions and rRNA deplete vs poly-A selection from Sultan et al.

All fastq files were trimmed to 50bp and aligned to hg38 with enzembl annotations in two-pass mode with STAR, with mostly default parameters.

Analysis of intron positions and general quantifications of splicing: How do the different datasets differ with where in the gene the splice sites are.

Analysis of cotranscriptional splicing by 3’ss ratio: Quantification of cotranscriptional splicing by comparing amount of splicing (as quantified by coverage before and after 3’ss) in nascent RNA-seq (chromatin associatied) versus standard RNA-seq.