Description Usage Arguments Value Examples
In our analysis we calculate frequencies prior to removing false positives. Sometimes this means we have a monomorphic site with the allele present at <100 in each case this holds true. That work is in 2017_11_13.Rmd- 2017_11_16.Rmd in the notebook directory of the HIVE repo. It is also true we will miss some true variants in the <10 frequenies of 1.
1 | monomorphic(df, ...)
|
df |
variant data frame |
... |
columns to group by. There's no current need for them to be anything but SPECID,season,chr,pos,pcr_result |
the input data frame but with monomorphic frequencies = 1.
1 2 3 | wacky_isnv<-small_isnv
wacky_isnv$freq.var[wacky_isnv$mutation=="PB2_G1602A"]<-0.8
monomorphic(wacky_isnv,SPECID,season,chr,pos,pcr_result)
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