DOTTER(1)

πŸ’– NAME πŸ’–

dotter β€” sequence dotplots with image enhancement tools ✨


πŸ¦‹ DESCRIPTION πŸ¦‹

okay so bestie, Dotter makes sequence dotplots and it comes with image enhancement tools built in. it's giving "genomics but make it cute." πŸ’…

here's the vibe of how you run it:

dotter [options] <horizontal_sequence> <vertical_sequence> [X options]

where <horizontal_sequence> and <vertical_sequence> are file names for FASTA files holding your two sequences. no cap, that's the whole ritual. πŸŽ€

🌸 allowed sequence types 🌸

not every combo is allowed, so let's do a vibe check:

  • Protein – Protein
  • DNA – DNA
  • DNA – Protein

✨ OPTIONS ✨

  • -h, --help β€” show this usage information. the "help me bestie" button 🫢
  • -b <file>, --batch-save=<file> β€” batch mode; save dot matrix to <file> πŸ’Ύ
  • -e <file>, --batch-export=<file> β€” batch mode; export plot to PDF file <file> πŸ“„
  • -l <file>, --load β€” load dot matrix from <file> πŸ™ˆ
  • -m <float>, --memory-limit=<float> β€” memory usage limit in Mb (default 0.5). yes, half a megabyte. she's frugal. 😭
  • -z <int>, --zoom β€” set zoom (compression) factor πŸ”
  • -p <int>, --pixel-factor β€” set pixel factor manually (ratio pixelvalue/score)
  • -W <int>, --window-size β€” set sliding window size. (K => Karlin/Altschul estimate) πŸ‘‘
  • -M <file>, --matrix-file=<file> β€” read in score matrix from <file> (Blast format; Default: Blosum62).
  • -F <file>, --sequence-file β€” read in sequences and data from <file> (replaces sequencefiles).
  • -f <file>, --feature-file β€” read feature segments from <file> 🧚
  • -H, --hsp-mode β€” do not calculate dotplot at startup.
  • -R, --reverse-greyramp β€” reversed Greyramp tool at start.
  • -r, --reverse-horizontal β€” reverse and complement horizontal_sequence (if DNA)
  • -v, --reverse-vertical β€” reverse and complement vertical_sequence (if DNA)
  • -D, --disable-mirror β€” don't display mirror image in self comparisons πŸͺž
  • -w, --watson-only β€” for DNA: horizontal_sequence top strand only (Watson)
  • -c, --crick-only β€” for DNA: horizontal_sequence bottom strand only (Crick)
  • -q <int>, --horizontal-offset=<int> β€” horizontal_sequence offset
  • -s <int>, --vertical-offset=<int> β€” vertical_sequence offset
  • --horizontal-type=p|d β€” horizontal_sequence type ('p' for peptide or 'd' for DNA)
  • --vertical-type=p|d β€” vertical_sequence type ('p' for peptide or 'd' for DNA)
  • --abbrev-title-on β€” abbreviate window title prefixes
  • --abbrev-title-off β€” do not abbreviate window title prefixes
  • --session_colour=<colour_str> β€” set the background colour of the dotter window 🎨
  • --compiled β€” show package compile date
  • --version β€” show package version

πŸ’œ the credits (iykyk) πŸ’œ

written by Gemma Barson <gb10@sanger.ac.uk>, based on original code by Erik Sonnhammer <Erik.Sonnhammer@sbc.su.se>.

reference: Sonnhammer ELL & Durbin R (1995). A dot-matrix program with dynamic threshold control suited for genomic DNA and protein sequence analysis. Gene 167(2):GC1-10.

see http://www.sanger.ac.uk/resources/software/seqtools/ for more info. 🌈

copyright (c) 2010-2015: Genome Research Ltd. Dotter is distributed under the GNU General Public License; see http://www.gnu.org/copyleft/gpl.txt ⭐

version 4.44.1 β€” 14:27:56 Oct 19 2017


πŸŽ€ AUTHOR πŸŽ€

this manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program. 🫢


and that's the whole page, bestie!! this little writeup is for dotter version 4.44.1, dated October 2017, and yes it's still the DOTTER(1) manual β€” go make some iconic dotplots, you've got this πŸ’–βœ¨πŸ¦‹πŸŒΈπŸ’