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Diffstat (limited to 'academic/pyCRAC/README')
| -rw-r--r-- | academic/pyCRAC/README | 24 |
1 files changed, 4 insertions, 20 deletions
diff --git a/academic/pyCRAC/README b/academic/pyCRAC/README index 9eb56fc04311f..b9b74fd37bac6 100644 --- a/academic/pyCRAC/README +++ b/academic/pyCRAC/README @@ -5,8 +5,10 @@ data generated by CLIP or CRAC protocols). It can be used to remove duplicate reads,tackles directional libraries and reports sense and anti-sense hits. -Included is the pipeline used for the analysis of a group of CRAC data -sets. +A pipeline that streamlines the analysis of a group of CRAC datasets +is available at https://git.ecdf.ed.ac.uk/sgrannem/crac_pipelines and +depends on the python package 'ruffus', also at slackbuilds.org. + References @@ -23,21 +25,3 @@ A, Langford A, Franklin R, Iosub I, Wadsworth P, Sanguinetti G, Granneman S. If you want to run the test suite after installation, see README.tests. - - -Note on the Crac pipelines: - -Use the -h flag to get a detailed help menu. - -The CRAC_pipeline_PE.py script needs to be run from the folder that -contains the fastq files - -The barcode list file should contain two tab-separated columns in which -the first column is the barcode sequence and the second column is the -name of the experiment - -The file containing the adapter sequences should be in the fasta format. - -The chromosome_lengths file should contain two tab-separated columns in -which the first column has the chromosome name and the second the -chromosome length. |