seqtools 4.44.1+dfsg-7build1 source package in Ubuntu
Changelog
seqtools (4.44.1+dfsg-7build1) jammy; urgency=medium * No-change rebuild against libjsoncpp25 -- Steve Langasek <email address hidden> Tue, 14 Dec 2021 07:52:17 +0000
Upload details
- Uploaded by:
- Steve Langasek
- Uploaded to:
- Jammy
- Original maintainer:
- Ubuntu Developers
- Architectures:
- any
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section | |
---|---|---|---|---|
Mantic | release | universe | misc | |
Lunar | release | universe | misc | |
Kinetic | release | universe | misc | |
Jammy | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
seqtools_4.44.1+dfsg.orig.tar.xz | 3.7 MiB | 7e29efb82712663868db18ba9234f07a774ef5f23082c82aa4a1780e8f4237a5 |
seqtools_4.44.1+dfsg-7build1.debian.tar.xz | 15.2 KiB | 23fc629b546872c87c4a80f97a9e6551652e89f01951431f34a9b9551c01056c |
seqtools_4.44.1+dfsg-7build1.dsc | 2.4 KiB | 525979e6380773c7314c57728f78e964bbbf4488f2b6d8413d50dfdc42a78fce |
Available diffs
Binary packages built by this source
- belvu: multiple sequence alignment viewer and phylogenetic tool
Belvu is a multiple sequence alignment viewer and phylogenetic tool with
an extensive set of user-configurable modes to color residues.
.
* View multiple sequence alignments.
* Residues can be coloured by conservation, with user-configurable
cutoffs and colours.
* Residues can be coloured by residue type (user-configurable).
* Colour schemes can be imported or exported.
* Swissprot (or PIR) entries can be fetched by double clicking.
* The position in the alignment can be easily tracked.
* Manual deletion of rows and columns.
* Automatic editing of rows and columns based on customisable criteria:
- removal of all-gap columns;
- removal of all gaps;
- removal of redundant sequences;
- removal of a column by a user-specified percentage of gaps;
- filtering of sequences by percent identity;
- removal of sequences by a user-specified percentage of gaps;
- removal of partial sequences (those starting or ending with
gaps); and
- removal of columns by conservation (with user-specified
upper/lower cutoffs).
* The alignment can be saved in Stockholm, Selex, MSF or FASTA format.
* Distance matrices between sequences can be generated using a variety
of distance metrics.
* Distance matrices can be imported or exported.
* Phylogenetic trees can be constructed based on various distance-based
tree reconstruction algorithms.
* Trees can be saved in New Hampshire format.
* Belvu can perform bootstrap phylogenetic reconstruction.
- belvu-dbgsym: debug symbols for belvu
- blixem: interactive browser of sequence alignments
Blixem is an interactive browser of sequence alignments that have been
stacked up in a "master-slave" multiple alignment; it is not a 'true'
multiple alignment but a 'one-to-many' alignment.
.
* Overview section showing the positions of genes and alignments around
the alignment window
* Detail section showing the actual alignment of protein or nucleotide
sequences to the genomic DNA sequence.
* View alignments against both strands of the reference sequence.
* View sequences in nucleotide or protein mode; in protein mode, Blixem
will display the three-frame translation of the reference sequence.
* Residues are highlighted in different colours depending on whether
they are an exact match, conserved substitution or mismatch.
* Gapped alignments are supported, with insertions and deletions being
highlighted in the match sequence.
* Matches can be sorted and filtered.
* SNPs and other variations can be highlighted in the reference
sequence.
* Poly(A) tails can be displayed and poly(A) signals highlighted in the
reference sequence.
- blixem-dbgsym: debug symbols for blixem
- dotter: detailed comparison of two genomic sequences
Dotter is a graphical dot-matrix program for detailed comparison of two
sequences.
.
* Every residue in one sequence is compared to every residue in the
other, and a matrix of scores is calculated.
* One sequence is plotted on the x-axis and the other on the y-axis.
* Noise is filtered out so that alignments appear as diagonal lines.
* Pairwise scores are averaged over a sliding window to make the score
matrix more intelligible.
* The averaged score matrix forms a three-dimensional landscape,
with the two sequences in two dimensions and the height of the
peaks in the third. This landscape is projected onto two
dimensions using a grey-scale image - the darker grey of a peak,
the higher the score is.
* The contrast and threshold of the grey-scale image can be adjusted
interactively, without having to recalculate the score matrix.
* An Alignment Tool is provided to examine the sequence alignment that
the grey-scale image represents.
* Known high-scoring pairs can be loaded from a GFF file and overlaid
onto the plot.
* Gene models can be loaded from GFF and displayed alongside the
relevant axis.
* Compare a sequence against itself to find internal repeats.
* Find overlaps between multiple sequences by making a dot-plot of all
sequences versus themselves.
* Run Dotter in batch mode to create large, time-consuming dot-plots as
a background process.
- dotter-dbgsym: debug symbols for dotter
- libgbtools-dev: library for visualising sequence alignments (devel)
The SeqTools package contains three tools for visualising sequence
alignments: Blixem, Dotter and Belvu.
.
This package contains the static library and header files.
- libgbtools0: library for visualising sequence alignments
The SeqTools package contains three tools for visualising sequence
alignments: Blixem, Dotter and Belvu.
.
This package contains the library all three tools are linked against.
- libgbtools0-dbgsym: debug symbols for libgbtools0