seqtools 4.44.1+dfsg-2 source package in Ubuntu

Changelog

seqtools (4.44.1+dfsg-2) unstable; urgency=medium

  * Versioned Conflicts+Replaces to enable installing old transitional packages
    Closes: #887616
  * Standards-Version: 4.1.3
  * debhelper 11

 -- Andreas Tille <email address hidden>  Mon, 22 Jan 2018 13:25:58 +0100

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Debian Med
Uploaded to:
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Original maintainer:
Debian Med
Architectures:
any
Section:
misc
Urgency:
Medium Urgency

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seqtools_4.44.1+dfsg-2.dsc 2.3 KiB 09f001e20289c6456d5412af191da46a5fc43a52d44c91bb120d71214fb3127a
seqtools_4.44.1+dfsg.orig.tar.xz 3.7 MiB 7e29efb82712663868db18ba9234f07a774ef5f23082c82aa4a1780e8f4237a5
seqtools_4.44.1+dfsg-2.debian.tar.xz 14.1 KiB 947756a450f3a35b8e3a9daf3d0661ddd3526561ea39821708c4bfa8a2c54a65

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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