DOTTER(1)
π NAME π
dotter β sequence dotplots with image enhancement tools β¨
π¦ DESCRIPTION π¦
okay so bestie, Dotter makes sequence dotplots and it comes with image enhancement tools built in. it's giving "genomics but make it cute." π
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. π
πΈ allowed sequence types πΈ
not every combo is allowed, so let's do a vibe check:
- Protein β Protein
- DNA β DNA
- DNA β Protein
β¨ OPTIONS β¨
-h,--helpβ show this usage information. the "help me bestie" button π«Ά-b <file>,--batch-save=<file>β batch mode; save dot matrix to<file>πΎ-e <file>,--batch-export=<file>β batch mode; export plot to PDF file<file>π-l <file>,--loadβ load dot matrix from<file>π-m <float>,--memory-limit=<float>β memory usage limit in Mb (default0.5). yes, half a megabyte. she's frugal. π-z <int>,--zoomβ set zoom (compression) factor π-p <int>,--pixel-factorβ set pixel factor manually (ratiopixelvalue/score)-W <int>,--window-sizeβ set sliding window size. (K=> Karlin/Altschul estimate) π-M <file>,--matrix-file=<file>β read in score matrix from<file>(Blast format; Default:Blosum62).-F <file>,--sequence-fileβ read in sequences and data from<file>(replaces sequencefiles).-f <file>,--feature-fileβ read feature segments from<file>π§-H,--hsp-modeβ do not calculate dotplot at startup.-R,--reverse-greyrampβ reversed Greyramp tool at start.-r,--reverse-horizontalβ reverse and complementhorizontal_sequence(if DNA)-v,--reverse-verticalβ reverse and complementvertical_sequence(if DNA)-D,--disable-mirrorβ don't display mirror image in self comparisons πͺ-w,--watson-onlyβ for DNA:horizontal_sequencetop strand only (Watson)-c,--crick-onlyβ for DNA:horizontal_sequencebottom strand only (Crick)-q <int>,--horizontal-offset=<int>βhorizontal_sequenceoffset-s <int>,--vertical-offset=<int>βvertical_sequenceoffset--horizontal-type=p|dβhorizontal_sequencetype ('p'for peptide or'd'for DNA)--vertical-type=p|dβvertical_sequencetype ('p'for peptide or'd'for DNA)--abbrev-title-onβ abbreviate window title prefixes--abbrev-title-offβ do not abbreviate window title prefixes--session_colour=<colour_str>β set the background colour of the dotter window π¨--compiledβ show package compile date--versionβ show package version
π the credits (iykyk) π
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. π
copyright (c) 2010-2015: Genome Research Ltd. Dotter is distributed under the GNU General Public License; see http://www.gnu.org/copyleft/gpl.txt β
version 4.44.1 β 14:27:56 Oct 19 2017
π AUTHOR π
this manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program. π«Ά
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 πβ¨π¦πΈπ
π¦ where this page comes from
- debian bookworm: dotter 4.44.1+dfsg-7+b2 Β· GPL-3.0-or-later
- debian trixie: dotter 4.44.1+dfsg-7.1+b3 Β· GPL-3.0-or-later
- ubuntu jammy: dotter 4.44.1+dfsg-7build1 Β· GPL-3.0-or-later
- ubuntu noble: dotter 4.44.1+dfsg-7.1build2 Β· GPL-3.0-or-later
- ubuntu questing: dotter 4.44.1+dfsg-7.1build3
- ubuntu resolute: dotter 4.44.1+dfsg-8 Β· GPL-3.0-or-later
- ubuntu stonking: dotter 4.44.1+dfsg-8 Β· GPL-3.0-or-later
- π girlified by deepseek-ai/DeepSeek-V4.1-Flash on : a language model's rewrite of the original, under its terms