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Bugfix 1: [triplet] Lengths (frameCounting) if given should be a range (not zero). readingFrame function fails with subscript out of bounds. Bugfix 2: [triplet] Check if transcript name in SAM matches the name in FASTA. Produce an error message if it's not. This fixes the problem where an empty plot is produced (no bars). [ribosome_profile] - A proper error message is now produced if an invalid transcript name is provided. Updated test data
author Vimalkumar Velayudhan <vimalkumarvelayudhan@gmail.com>
date Tue, 27 Oct 2015 12:21:50 +0000
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1 README
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4 `riboSeqR <http://bioconductor.org/packages/3.0/bioc/html/riboSeqR.html>`_
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5 integration for `Galaxy <http://galaxyproject.org/>`_ /
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6 `RiboGalaxy <http://ribogalaxy.ucc.ie/>`_.
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8 Included tools
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9 ..............
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10 In the order in which they are run
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12 #. Prepare riboSeqR Input
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14 Prepare riboSeqR format input files from alignment files (SAM format,
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15 Ribo-Seq or RNA-Seq alignments).
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17 #. Triplet Periodicity
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19 Plot triplet periodicity for different read lengths.
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21 #. Metagene Analysis
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23 Metagene analysis.
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25 #. Plot Ribosome Profile
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27 Plot Ribosome profile and output Ribo/RNA counts.
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29 [OR]
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31 Differential Translation Analysis
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33 Get Ribo and RNA-Seq counts with riboSeqR. Perform differential
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34 translation analysis with baySeq.
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36 Tested with
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37 ...........
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38 **R** ``3.1.2``
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40 **riboSeqR** ``1.0.5``
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42 **baySeq** ``2.0.50``
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44 **rpy2** ``2.3.10``