Author: Daniel P. Howrigan
Start Date: January 2016
Welcome! This repository is a collection of R scripts used to analyze array-based CNV. The primary aim is to get you familiar with looking at CNV descriptive statistics for potential issues, and running CNV burden and individual locus association. I've added a small example dataset that mimics a number of proprties and issues related to large-scale CNV analysis. If all works well, the scripts provided should be able to run on the example dataset, and should give you some background to pursue more detailed and refined analyses on your own CNV data.
The example dataset contains 2000 individuals from 4 separate datasets. I have anonymized the IDs to prevent any re-identification with the randomly selected samples. The data is a formatted version of CNV calls that allow for CNV analysis in PLINK, and the phenotypes (.phe) have a selected set of principle components that were calculated from GWAS. For data management purposes outside of this example, it is critically important that the sample identifiers for array CNV data and their resepective principal component scores from array GWAS data have been properly matched
As currently stands, the CNV calls and additional genomic location files use NCBI36/hg18 genomic positions - you can use the LiftOver tool in the UCSC browser to update positions to more recent genome builds, however sometimes this can be a pain, and not worth your effort for the example dataset. If you want to use more recent genome builds in your analysis, I would suggest lifting over all files with positions (including CNV lists, gene lists, candidate CNV lists, pathways, etc..) as early as possible
For the principal components, I've included 5 PCs that showed association to small CNV (< 100 kb) burden in previous analysis, however the relevant PCs used will likely vary from dataset to dataset. Of note, there may be other relevant covariates for each study, and this example is not necessarily a guide of which covariates are, or are not, important in any given analysis framework.
As these files closely follow the format of PLINK CNV files, and it is best to look at the PLINK documentation for full details: pngu.mgh.harvard.edu/~purcell/plink/cnv.shtml
CNV_data.cnv - CNV calls
FID = Family ID (unique identifier across all datasets)
IID = Individual ID (unique identifier within each dataset)
CHR = Chromosome
BP1 = CNV start position
BP2 = CNV end position
TYPE = 1 is deletion or copy number loss, 3 is duplication or copy number gain
SCORE = Can be any value of interest for CNV - Here it is the number of genes overlapping the CNV provided by the original CNV calls
SITES = number of genotyped SNPs in the CNV
CNV_data.fam - pedigree file
FID = Family ID
IID = Individual ID
PID = Paternal ID (set to zero)
IID = Maternal ID (set to zero)
SEX = male=1/female=2
AFF = Affection status (unaffected=1,affected=2)
CNV_data.phe - Phenotype file
FID
IID
AFF = Affection status (control=1,case=2)
SEX (male=1,female=2)
ancestry = eur (European)
CNV_platform = Genotyping chip used to call CNVs
C1 to C8 = Principal Components 1,2,3,4, and 8 from GWAS
I've also included a few additional files that are often used. A candidate CNV list, which list the genomic positions of selected regions for exlcusion or inclusion (hg18_implicated_CNV.txt), and a gene list (hg18_refGene_plink.txt) to map CNVs to specific genes.
These scripts are meant to run interactively in the R environment, and contain documentation for submitting longer running jobs on the command line. Do not run these scripts from the command line until you've optimized them yourself for automation. Each script has an overview of what the script does and what files / programs are needed. All scripts assume you are running from the same directory with the cnv files, and will sometimes create subdirectories for output files.
CNV_data_descriptives.R
This script looks at the phenotype data for potential issues, errors, or outliers in data quality, and provides a few graphical examples for looking at the distribution of CNVs.
Main steps:
- Checking case/control balance
- Checking CNV burden by dataset / platform
- Checking CNV burden by PC
CNV_burden_level_association.R
This script has steps to run a detailed CNV burden analysis, look at the results, and make a forest plot of the results.
Main steps:
- Running CNV burden script
- specify parameters to view and graph
- show main results
- Forest plot
CNV_SNP_level_association.R
This script has steps to run CNV association analysis, generate residual phenotypes, get genome-wide correction estimates, and make UCSC .bed and .bedGraph files.
Main steps:
- Case/control association: CNV_CaseCon_assoc.R
- Residual phenotype generation
- Residual phenotype association: CNV_assoc_Quantitative.R
- Family-wise error correction
- Manhattan Plot
- UCSC .bed and .bedGraph files
After creating UCSC .bed and .bedGraph files, you can upload them to the UCSC browser using "custom tracks" upload in the "My Data" menu or straight from the home page. Remember to use good 'ol NCBI36/hg18 coordinates!
These scripts are meant to run as submitted jobs, and usually have a set of arguments that are passed to the script. Each script has an overview of what the script does and what files / programs are needed. All scripts assume you are running from the same directory with the cnv files, and will sometimes create subdirectories for output files. As written in the interactive R scripts, these were run on the LSF cluster at the Broad Institute, and you will need to make adjustments to the submission prompts for your specific server. FOr the exmaple dataset, most of these scripts should run on your own computer, however larger numbers of permutations could take a while.
CNV_burden_platform.R
This is the most intensive of the scripts used here, and it is worth looking at the documentation to understand what is going on. This script runs CNV burden analyses on a variety of datasets, CNV types, and CNV property filters. Once you are familiar with the filters, you can add/substract additional filters that may be worth investigating.
Main steps:
- CNV burden filters
- CNV burden loop
- Applying PLINK filters
- Reading PLINK burden results
- CNV burden analysis in R
- Combining all results together and writing to file
CNV_assoc_CaseCon.R
A short script to run PLINK CNV association on case/control data.
CNV_assoc_Quantitative.R
Another short script to run PLINK CNV association on quantitative data, which is used when including covariates for analysis.
Manhattan.R
A short script to help create Manhattan plots of the results
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