Takes an input set of intervals and for each interval determines the base coverage of the interval by a set of features (tables) available from UCSC. Genomic regions from the input feature data have been merged by overlap / direct adjacency (e.g. a table having ranges of: 1-10, 6-12, 12-20 and 25-28 results in two merged ranges of: 1-20 and 25-28). |
hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/annotation_profiler
Repository package_bx_python_0_7 revision 2d0c08728bca owned by devteam |
Name | Version | Type | |
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bx-python | 0.7.1 | package |
Name | Description | Version | Minimum Galaxy Version |
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for a set of genomic intervals | 1.0.0 | any |