Open adamklie opened 9 months ago
Hi Adam, sorry for the late reply. I save the outputs for each 249bp sequence tiled across the genome, and average them per nucleotide (across all overlapping tiles) to obtain genome-wide coverage. I used GenomicRanges in R for computing this coverage and rtracklayer to save as bigWigs. The STARR-seq bigWigs are in linear scale but the model predicts values in log scale, so you have to convert the predictions back to linear scale to match the STARR-seq ones.
Hey Bernardo!
Random question. When you predict across the dm3 genome, how do you save the outputs and then convert them to bigWig tracks that nicely match the STARR-seq bigWigs in magnitude? Maybe convert the predictions to bigBed and then use something like bigBedToBigWig.sh?
Adam