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  • Home > Linux > Science and Engineering > Bioinformatics

    Staden Package 1.7.0 / 2.0.0 Beta 8

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    Last Updated:

    Category:
    Andrew Whitwham, James Bonfield and Mark Griffiths | More programs
    BSD License / FREE
    February 9th, 2011, 12:32 GMT
    ROOT / Science and Engineering / Bioinformatics

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    Staden Package description

    Staden Package is a fully developed set of DNA sequence assembly, editing and analysis tools.

    Staden Package is a fully developed set of DNA sequence assembly (Gap4), editing and analysis tools (Spin) for Unix, Linux, MacOSX and MS Windows.

    On the Gap4 front there have been several minor joining related
    improvements in how it scores joins in Find Internal Joins and the
    functionality of the align button in the Join Editor.

    Also of consequence to gap4 are the various changes to io_lib (the
    library for all I/O to various trace file formats). With the addition
    of a new hash_exp program it now allows for experiment files to be
    concatenated together and indexed. The list of experiment file names
    should stil be supplied to gap4, but provided the EXP_PATH environment
    variable has been set correctly gap4 will be able to fetch individual
    sequences out of the concatenated experiment file
    archive. Improvements to the user interface for this still need to be
    made.

    454 SFF archives are now better supported. The defsult 454 indices
    now work, although the hash_sff program can be used to provide an
    alternative indexing strategy (possibly faster in some cases).

    Gap4 and trev also have another trace display style for traces that
    have 1 sample scan (x4 channels) per base call. In this case it can
    also draw 4 confidence values instead of 1 per base. These abilities
    will allow better integration of Solexa traces when more readily
    available.

    Plus of course the usual mix of bug fixes and minor tweaks. See the
    full change log for details (via the SourceForge site).

    Other notable changes

    Gap4

    · Various SNP Candidates improvements. The "correlation offset" is now
    adjustable (this controls the average correlation score needed
    before groups are considered for automatic merging). SNP base calls
    now work by generating a consensus rather than requiring 100%
    identity. it now skips sequences containing a REFS note. Merging can
    be forced until the number of groups is less than or equal to a
    predetermined amount (NB: not usually ideal).

    · Shuffle pads now has a "band size" parameter for the alignments.
    Also bug fixed in various places.

    · The old editor shuffle command has been replaced by strip pads. It
    now only removes entire columns of pads and does no pad movement at
    all.

    · The join editor align button will now cope better with handling long
    alignments in repeated data, hopefully avoiding the "too long for
    practical use of dynamic programming" message in such cases.

    It also now has "" buttons either side of the "Align"
    button. These anchor one end of the alignment to the current overlap
    position and then only align from that point leftwards or
    rightwards. This helps to force an alignment to anchor at a specific
    location which is useful when aligning data consisting of multiple
    repeat elements.

    · Alignments found by Find Internal Joins now take into account the
    alignment score in addition to the percentage identity. This means
    that no longer will a 100bp overlap at 100% identity be considered
    as a better overlap than a 2kb overlap at 99% identity.

    · The Contig Navigation window now has Page Up and Page Down
    keybindings for previous and next match. It also has the ability to
    automatically display traces at the appropriate regions using the
    contig editors "Auto-display traces" functionality.

    · The "View List" window now has a Save button.

    Io_lib

    · New programs: hash_exp, hash_sff, append_sff, extract_fastq.

    · Added TRACE_PATH and EXP_PATH environment variables to use in
    preference to RAWDATA (when defined).

    · Now uses libcurl instead of wget for much faster web based trace
    fetching.

    Product's homepage

      


    TAGS:

    DNA sequence | sequence assembly | data analyzer | DNA | sequence | assembly

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