NgsRelate: Difference between revisions
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=Brief description= | =Brief description= | ||
This page contains information about the program called NgsRelate, which can be used to infer relatedness coefficients for pairs of individuals for low coverage | This page contains information about the program called NgsRelate, which can be used to infer relatedness coefficients for pairs of individuals for low coverage Next Generation Sequencing (NGS) data by using genotype likelihoods. To be able to infer the relatedness you will need to know the population frequencies and have genotype likelihoods. This can be obtained e.g. using the program ANGSD as shown in the example below. | ||
=Download and Installation= | =Download and Installation= |
Revision as of 22:46, 19 June 2015
Brief description
This page contains information about the program called NgsRelate, which can be used to infer relatedness coefficients for pairs of individuals for low coverage Next Generation Sequencing (NGS) data by using genotype likelihoods. To be able to infer the relatedness you will need to know the population frequencies and have genotype likelihoods. This can be obtained e.g. using the program ANGSD as shown in the example below.
Download and Installation
Primary repository is github. https://github.com/ANGSD/NgsRelate
curl https://raw.githubusercontent.com/ANGSD/NgsRelate/master/NgsRelate.cpp >NgsRelate.cpp g++ NgsRelate.cpp -O3 -lz -o NgsRelate
Run example using only ngs data
Assume we have file containing paths to 100 BAM/CRAM files, then we can use ANGSD to estimate frequencies calculate genotype likelihoods while doing SNP calling and dumping the input files needed for the NgsRelate program
./angsd -b filelist -gl 1 -domajorminor 1 -snp_pval 1e-6 - domaf 1 -minmaf 0.05 -doGlf 3 #this generates an angsdput.mafs.gz and a angsdput.glf.gz. #we will need to extract the frequency column from the mafs file and remove the header cut -f5 angsdput.mafs.gz |sed 1d >freq ./ngsrelate -g angsdput.glf.gz -n 100 -f freq -a 0 -b 1 >gl.res
Here we specify that our binary genotype likelihood file contains 100 samples, and that we want to run the analysis for the first two samples -a 0 -b 1. If no -a and -b are specified it will loop through all pairs
Output
Example of output
Pair k0 k1 k2 loglh nIter coverage (0,1) 0.673213 0.326774 0.000013 -1710940.769941 19 0.814658
The first column contain the individuals that was used for the analysis . The next three columns are the estimated relatedness coefficient, the likelihood of the MLE, the number of iterations required to find optima, and finally the fraction of non missing sites. This is the fraction of sites where we have data for both samples, and a MAF above the default threshold.
Input file format
The input files are binary gz compressed, log like ratios encoded as double. 3 values per sample. The freq file is allowed to be gz compressed.
Citing and references
Changelog
See github for log