# NOT RUN {
# cat(">Population1_sequence1",
# "TTATAAAATCTA----TAGC",
# ">Population1_sequence2",
# "TAAT----TCTA----TAAC",
# ">Population1_sequence3",
# "TTATAAAAATTA----TAGC",
# ">Population1_sequence4",
# "TAAT----TCTA----TAAC",
# ">Population2_sequence1",
# "TTAT----TCGA----TAGC",
# ">Population2_sequence2",
# "TTAT----TCGA----TAGC",
# ">Population2_sequence3",
# "TTAT----TCGA----TAGC",
# ">Population2_sequence4",
# "TTAT----TCGA----TAGC",
# ">Population3_sequence1",
# "TTAT----TCGAGGGGTAGC",
# ">Population3_sequence2",
# "TAAT----TCTA----TAAC",
# ">Population3_sequence3",
# "TTATAAAA--------TAGC",
# ">Population3_sequence4",
# "TTAT----TCGAGGGGTAGC",
# file = "ex2.fas", sep = "\n")
# library(ape)
# example<-read.dna(file="ex2.fas",format="fasta")
#
# # Exclude unique haplotypes
# FilterHaplo(align=example,Nmin=2)
#
# # Include only unique haplotypes
# FilterHaplo(align=example,Nmax=1)
#
# # Filter haplotypes appearing between 2 and 4 times
# FilterHaplo(align=example,Nmax=4,Nmin=2)
# }
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