For a specific patient, report integration near oncogenes and potentially expanded clones across cell types and multiple time points
Report is done for individual patient for multiple timepoints and cell types, each corresponding to unique GTSP. For each sample multiple preps can be used.
Sample name corresponds to name used in integration site calling DB.
Format is (tab-separated):
GTSP sampleName
- The patient report is done for a single patient.
- All sites should be computed based on one reference genome.
- All sample names and GTSPs should exist in intSite and specimen managemnet databases.
config file should be in home directory and called .my.cnf, e.g. ~/.my.cnf
The .my.cnf format is as follows:
[intSitesDEV-dev]
user=YYYYYYY
password=XXXXXX
host=microb98.med.upenn.edu
port=3309
database=intsitesdev
intSiteRetriever : https://github.com/esherm/intSiteRetriever (at present get the project in current folder:
git clone https://github.com/esherm/intSiteRetriever
```)
hiAnnotator
reldist
Cancer Gene list:
git clone https://github.com/anatolydryga/CancerGeneList.git
# Testing
Run in the R console:
```bash
library(testthat)
test_dir(".")