How to not include start region in analyzing ribosome profiling data?
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@nicholsonangela7-13852
Last seen 6.6 years ago
UCSD

Hi,
I am new to ribosome profiling but am hoping I can use the RiboProfiling package for analyzing my data. I want to customize where I am looking for protected fragments though because I would like to not include the start region (the first 50 nucleotides) for all transcripts as it can sometimes result in a biased comparison between genes. Is there a way I can use this package and specify that I would like to not count reads that fall on the first 50 nucleotides of every transcript? I tried using the listshiftvalue parameter but the output I got in the data.frame is the same as when I didn't add 50 there so I think this must be the wrong place. 
covData <- riboSeqFromBAM(listInputBam, txdb = txdb, listShiftValue=c(50))

Thank you! 

Angela Nicholson

 

 

 

riboprofiling ribosome profiling • 705 views
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