View source: R/processVCFfast.R
For a SNP with aberrant digestion sites in the context, randomly change bases in the site across barcodes
1 | randomly_fix(snp, res_df, dig_patterns, dig_site_locations)
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snp |
a data_frame of one SNP #' @param nper The number of barcoded sequences to be generated per allele per SNP |
upstreamContextRange |
the amount of sequence context to acquire upstream of the SNP |
downstreamContextRange |
the amount of sequence context to acquire downstream of the SNP |
fwprimer |
a string containing the forward PCR primer to be used |
revprimer |
a string containing the reverse PCR primer to be used |
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