DOTTER:(1) General Commands Manual DOTTER:(1)NAME
dotter - Sequence dotplots with image enhancement tools.
SYNOPSIS
dotter [options] <horizontal_sequence> <vertical_sequence> [X options]
DESCRIPTION
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.
Allowed types:
Protein - Protein DNA - DNA DNA - Protein
Options:
-b <file>
Batch mode, write dotplot to <file>
-l <file>
Load dotplot from <file>
-m <float>
Memory usage limit in Mb (default 0.5)
-z <int>
Set zoom (compression) factor
-p <int>
Set pixel factor manually (ratio pixelvalue/score)
-W <int>
Set sliding window size. (K => Karlin/Altschul estimate)
-M <file>
Read in score matrix from <file> (Blast format; Default: Blosum62).
-F <file>
Read in sequences and data from <file> (replaces sequencefiles).
-f <file>
Read feature segments from <file>
-H Do not calculate dotplot at startup.
-R Reversed Greyramp tool at start.
-r Reverse and complement horizontal_sequence (DNA vs Protein)
-D Don't display mirror image in self comparisons
-w For DNA: horizontal_sequence top strand only (Watson)
-c For DNA: horizontal_sequence bottom strand only (Crick)
-q <int>
Horizontal_sequence offset
-s <int>
Vertical_sequence offset
Some X options: -acefont <font> Main font. -font <font> Menu font.
SEE ALSO
http://www.cgb.ki.se/cgb/groups/sonnhammer/Dotter.html for more info.
AUTHOR
Erik.Sonnhammer@cgb.ki.se Version 3.1, compiled Jul 10 2010
July 2010 DOTTER:(1)
Check Out this Related Man Page
SIBsim4(1) User Manuals SIBsim4(1)NAME
SIBsim4 - align RNA sequences with a DNA sequence, allowing for introns
SYNOPSIS
SIBsim4 [ options ] dna rna_db
DESCRIPTION
SIBsim4 is a similarity-based tool for aligning a collection of expressed sequences (EST, mRNA) with a genomic DNA sequence.
Launching SIBsim4 without any arguments will print the options list, along with their default values.
SIBsim4 employs a blast-based technique to first determine the basic matching blocks representing the "exon cores". In this first stage,
it detects all possible exact matches of W-mers (i.e., DNA words of size W) between the two sequences and extends them to maximal scoring
gap-free segments. In the second stage, the exon cores are extended into the adjacent as-yet-unmatched fragments using greedy alignment
algorithms, and heuristics are used to favor configurations that conform to the splice-site recognition signals (e.g., GT-AG). If neces-
sary, the process is repeated with less stringent parameters on the unmatched fragments.
By default, SIBsim4 searches both strands and reports the best matches, measured by the number of matching nucleotides found in the align-
ment. The R command line option can be used to restrict the search to one orientation (strand) only.
Currently, four major alignment display options are supported, controlled by the A option. By default, only the endpoints, overall similar-
ity, and orientation of the introns are reported. An arrow sign ('->' or '<-') indicates the orientation of the intron. The sign `=='
marks the absence from the alignment of a cDNA fragment starting at that position.
In the description below, the term MSP denotes a maximal scoring pair, that is, a pair of highly similar fragments in the two sequences,
obtained during the blast-like procedure by extending a W-mer hit by matches and perhaps a few mismatches.
OPTIONS -A <int>
output format
0: exon endpoints only
1: alignment text
3: both exon endpoints and alignment text
4: both exon endpoints and alignment text with polyA info
Note that 2 is unimplemented.
Default value is 0.
-C <int>
MSP score threshold for the second pass.
Default value is 12.
-c <int>
minimum score cutoff value. Alignments which have scores below this value are not reported.
Default value is 50.
-E <int>
cutoff value.
Default value is 3.
-f <int>
score filter in percent. When multiple hits are detected for the same RNA element, only those having a score within this percentage
of the maximal score for that RNA element are reported. Setting this value to 0 disables filtering and all hits will be reported,
provided their score is above the cutoff value specified through the c option.
Default value is 75.
-g <int>
join exons when gap on genomic and RNA have lengths which differ at most by this percentage.
Default value is 10.
-H <int>
report chimeric transcripts when the best score is lower than this percentage of the overall RNA coverage and the chimera score is
greater than this percentage of the RNA length (0 disables this report)
Default value is 75.
-I <int>
window width in which to search for intron splicing.
Default value is 6.
-K <int>
MSP score threshold for the first pass.
Default value is 16.
-L <str>
a comma separated list of forward splice-types.
Default value is "GTAG,GCAG,GTAC,ATAC".
-M <int>
scoring splice sites, evaluate match within M nucleotides.
Default value is 10.
-o <int>
when printing results, offset nt positions in dna sequence by this amount.
Default value is 0.
-q <int>
penalty for a nucleotide mismatch.
Default value is -5.
-R <int>
direction of search
0: search the '+' (direct) strand only
1: search the '-' strand only
2: search both strands
Default value is 2.
-r <int>
reward for a nucleotide match.
Default value is 1.
-S <int>
splice site indels search breadth. While determining the best position of a splice site, SIBsim4 will evaluate adding at most this
number of insertions and deletions on the DNA strand on each side of the splice junction.
Default value is 2.
-s <int>
split score in percent. While linking MSP, if two consecutive group of exons appear like they could be part of two different copies
of the same gene, they will be tested to see if the score of each individual group relative to the best overall score is greater
than this value. If both groups have a relative score above this threshold they will be split.
Default value is 75.
-W <int>
word size.
Default value is 12.
-X <int>
value for terminating word extensions.
Default value is 12.
Bioinformatics April 2007 SIBsim4(1)