View source: R/getBaseModificationDf.R
getBaseModificationDf.BSseq | R Documentation |
This function retrieve the information of each base, requiring BSseq object as input. Then organized it to dataframe.
getBaseModificationDf.BSseq(
region,
input,
BSgenome,
cover_depth = TRUE,
base = NULL,
motif = NULL,
position_bias = NULL
)
region |
base modification region in the form of dataframe, having columns of "chr","start" and "end" |
input |
the input data stored in BSseq objects |
BSgenome |
genome reference |
cover_depth |
take the depth of cover into account or not |
base |
one of A/T/G/C/U |
motif |
the motif(e.g C:CG/CH, A:GAGG/AGG) of the base modification |
position_bias |
1-base bias. e.g position_bias = 1("C" in "CHH"), position_bias = 2("A" in "GAGG") |
dataframe
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