#should probably have given up on shell and gone over to python.
+source $(dirname $0)/my_seq.sh
infile=$1
pg=$2
convert -blur 10 -gamma 0.00001 -median 1 $infile -resize 1x601\! -gamma 0.3 $dir/strip-${pg}-${subpg}.png
#There seems to be a definte bias in my reader scans for things to be in the top part rather than the bottom part
-testpoints=`jot - 270 320`
+testpoints=`$my_seq 270 320`
sum=0
prev=0