Two suggestions
  1. You do not need the for loop at all, you are merely counting to 30 and doing something once when you reach a magic number. This is particularly true if the starting dna sequence is greater than 30 bases.
  2. A look up table would be faster then an "until we get a different answer", this is particularly true if you are going to mutate your starting sequence repeatedly.
Try this for example
#!/usr/bin/perl use strict; use warnings; print "The DNA sequence is : \n" ; my $seq = 'AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA'; print "$seq \n"; mutate ($seq); exit; sub mutate{ my($dna) = shift; my $position = randposition($dna); print " mutation at base position ". ($position+1) . "\n"; my $nucleotide = randombase(substr($dna,$position,1)); substr($dna, $position, 1, $nucleotide); print "$dna\n"; } sub randposition{ my($sequence) = @_; return int rand length($sequence); } sub randombase{ my $base=shift; my(%nucleo)=( 'A'=>['T','C','G'], 'T'=>['A','C','G'], 'C'=>['A','T','G'], 'G'=>['A','T','G'], ); return $nucleo{$base}[rand(@{$nucleo{$base}})]; }

print "Good ",qw(night morning afternoon evening)[(localtime)[2]/6]," fellow monks."

In reply to Re: Help regarding the outout of the program by Utilitarian
in thread Help regarding the outout of the program by minnie

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