Description Usage Arguments Value
Detects potential splice sites in the proximal region of the input genomic coordinates. The function implements the prediction model proposed by Shapiro and Senapathy (Shapiro MB, Senapathy P. Nucleic Acids Research. 1987;15(17):7155-7174.)
1 | findSpliceSites(bed.data, persim = 0.8, offset = 10)
|
bed.data |
A data frame containing input bed-formatted data |
persim |
Similarity with the splice site consensus (default:0.8, range between [0,1]) |
offset |
Number of nucleotides expanded in each direction (default:10, min:5, max:50) |
1/ A detailed table with the location of the detected splice sites in each sequence and the corresponding similarity score
2/ A summary table with the number of splice sites detected in each sequence (input 'meinter' function)
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