Name | Modified | Size | Downloads / Week |
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README | 2019-04-24 | 3.1 kB | |
SpliceGrapher-0.2.7.tgz | 2019-04-24 | 21.5 MB | |
SpliceGrapher-0.2.6.tgz | 2017-09-07 | 21.4 MB | |
SpliceGrapher-0.2.5.tgz | 2016-09-29 | 21.4 MB | |
SpliceGrapher-0.2.4.tgz | 2013-12-19 | 21.4 MB | |
RNA-Seq-tutorial.tgz | 2013-08-30 | 93.5 MB | |
SpliceGrapher-0.2.3.tgz | 2013-08-30 | 21.4 MB | |
SpliceGrapher-0.2.2.tgz | 2013-03-19 | 21.3 MB | |
SpliceGrapher-0.2.1.tgz | 2012-12-10 | 21.2 MB | |
SpliceGrapher-0.2.0.tgz | 2012-09-28 | 20.8 MB | |
SpliceGrapher-0.1.0.tgz | 2012-04-03 | 788.0 kB | |
SpliceGrapher-0.0.5.tgz | 2011-09-30 | 640.7 kB | |
SpliceGrapher-0.0.4.tgz | 2011-07-25 | 468.2 kB | |
SpliceGrapher-0.0.3.tgz | 2011-04-18 | 444.6 kB | |
SpliceGrapher-0.0.2.tgz | 2011-04-13 | 480.3 kB | |
Totals: 15 Items | 266.6 MB | 1 |
SpliceGrapher - predicting splice graphs from diverse evidence Mark F. Rogers rogersma@cs.colostate.edu Version 0.2.7 released Description =========== SpliceGrapher is a Python-based scripting tool that uses gene models, RNA-Seq data and ESTs to predict splice graphs that capture in a single structure all the ways in which a gene's exons may be assembled. In a splice graph, a gene's exons are depicted as vertices and introns are depicted as edges between them. The compact structure allows researchers to visualize a gene's AS patterns more easily than by examining separate transcripts. SpliceGrapher includes modules that may be incorporated anywhere in an RNA-Seq analysis pipeline from initial alignment to final splice graph prediction. The package includes modules for constructing a database of known, recombined and predicted splice-junction sequences that may be used with ungapped short-read alignment algorithms such as MAQ, BowTie or PASS. The prediction modules are able to incorporate gene models in GFF3 format, RNA-Seq alignments in SAM format or EST alignments in PSL format. The viewing modules are able to read these same files to produce plots that depict a predicted graph along with the evidence SpliceGrapher used to produce it. Currently SpliceGrapher supports RNA-Seq alignments in SAM, BED and WIG formats, EST alignments in PSL format and Cufflinks transcript descriptions in GTF format. Installation ============ Only Unix/Linux/OS-X is supported. Requirements: matplotlib http://matplotlib.sourceforge.net (version 2.1.0 or higher) PyML http://sourceforge.net/projects/PyML (version 0.7.14 or higher) A setup.py script is provided so installation follows the standard python idiom: >>> python setup.py build >>> python setup.py install To install in a different directory than the system default, use >>> python setup.py install --home=/my/python/packages You may also install the stand-alone scripts in their own separate directory using the format: >>> python setup.py install --home=/my/python/packages --install-scripts=/my/python/scripts Updating paths ================== Before you run SpliceGrapher scripts, you will want to add the correct path to your PATH environment variable. By default this will be the /bin directory directly under the main installation directory. If you chose a different script path using the --install-scripts option, then use that path instead. If you used '--home=' to specify a home directory other than the default, you must ensure that it is included in your PYTHONPATH directory before you try to access SpliceGrapher's modules from python. Running Examples ================ The 'examples' subdirectory of the distribution contains example data and a shell script for creating splice graphs for the example data. To test your installation, simply run the script: >>> cd examples >>> run_tests.sh This script also provides examples to get you started using the SpliceGrapher Python scripts with your own data. Documentation ============= User Guide - doc/userguide.pdf Examples - SpliceGrapher/examples