require(big.phylo)
data(nz_h3n2)
# H3N2 data is stored in 'seq' DNAbin matrix object
print( seq )
# write sequences to directory for processing
indir <- getwd()
infile <- 'nz_h3n2.R'
insignat <- ''
save(seq, file=paste(indir, infile, sep='/'))
# create the command string
bs.id <- 1
infile <- substr(infile, 1, nchar(infile)-2)
argv <<- cmd.examl.bsalignment(indir, infile, bs.id)
argv <<- unlist(strsplit(argv,' '))
# create the bootstrap alignment
prog.examl.getbootstrapseq()
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