read.scf
or read.abif
as appropriate and then calling sangerseq
.readsangerseq(filename)
sangerseq
s4 objectread.abif
, read.scf
, abif
,
scf
, sangerseq
hetsangerseq <- readsangerseq(system.file("extdata",
"heterozygous.ab1",
package = "sangerseqR"))
str(hetsangerseq)
#same for scf files
homosangerseq <- readsangerseq(system.file("extdata",
"homozygous.scf",
package = "sangerseqR"))
str(homosangerseq)
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