Quick Start
From PileLine
(Difference between revisions)
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==PipeLine Guided example== | ==PipeLine Guided example== | ||
| - | '''1.''' Download GP example files (pileup format): | + | '''1.''' Download GP example files (pileup format) to your working directory: |
:[[File:Control1Files.zip]] | :[[File:Control1Files.zip]] | ||
| Line 24: | Line 24: | ||
'''2.''' You may compare Case1 vs Control1 at variant level using this command line: | '''2.''' You may compare Case1 vs Control1 at variant level using this command line: | ||
| - | + | cd DOWNLOADED_FILES_DIRECTORY | |
| + | sh YOUR_PATH_TO_PILELINE/cmd/pileline-2smc.sh | ||
| + | –a ./Control1.pileup –b ./Case1.pileup | ||
| + | –v ./Control1varfilter.pileupt –w ./Control2varfilter.pileup | ||
| + | –o ./myoutput.txt | ||
| + | Executing this code you will obtain: | ||
| + | * Variants found in Case1 but not in Control1 (i.e. somatic point mutations) | ||
| + | * Variants found in Case1 and in Control1 (i.e. germinal mutations or SNPs) | ||
: somatic mutations (Variants found in Case but not in Control) | : somatic mutations (Variants found in Case but not in Control) | ||
Revision as of 14:51, 18 June 2010
PipeLine input files
PileLine is capable to handle, filter and compare genomic position files (GP) including standard pileup, BED,GFF, or VCF files.
Basically, GP are tabular files where the two first columns contain chromosome name and position coordinate respectively. Additional optional fields may be added by users, see a GP file example below:
10 118829 optional1 optional2 optional3 ... 10 121207 optional1 optional2 optional3 ... 10 121337 optional1 optional2 optional3 ... 10 121636 optional1 optional2 optional3 ...
PipeLine Guided example
1. Download GP example files (pileup format) to your working directory:
Each .zip file contains 2 pileup files:
- Whole pileup file
- Variants (vs reference genome) pileup file.
2. You may compare Case1 vs Control1 at variant level using this command line:
cd DOWNLOADED_FILES_DIRECTORY
sh YOUR_PATH_TO_PILELINE/cmd/pileline-2smc.sh –a ./Control1.pileup –b ./Case1.pileup –v ./Control1varfilter.pileupt –w ./Control2varfilter.pileup –o ./myoutput.txt
Executing this code you will obtain:
- Variants found in Case1 but not in Control1 (i.e. somatic point mutations)
- Variants found in Case1 and in Control1 (i.e. germinal mutations or SNPs)
- somatic mutations (Variants found in Case but not in Control)
