NgsRelate

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

Run example using NGS data with plink population frequencies

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

### extract population from huge binary plink file
plink --bfile hapmap3_r2_b36_fwd.consensus.qc.polyHg19 --keep LWK.fam  --make-bed --out hapmap3Hg19LWK --noweb

### calculate frequencies for the subpopulation
plink --bfile  hapmap3Hg19LWK --freq --noweb --out LWKsub

### we are only interested in the output from the snpsites with the seq data. so we extract the chr,pos,major,minor
cut -f1,4-6  hapmap3Hg19LWK.bim >forAngsd.txt

### index the file for angsd
angsd sites index forAngsd.txt

##assuming 'list' contains path to bams
angsd -gl 1 -doglf 3 -sites forAngsd.txt -b list -domajorminor 3 -P 2 -minMapQ 30 -minQ 20
#this generates an angsdput.glf.gz and a angsdput.glf.pos.gz.

#extract the frequencies and sync it to the angsd output
 ./NgsRelate/a.out extract_freq angsdput.glf.pos.gz files/hapmap3Hg19LWK.bim files/LWKsub.frq >freq

#run ngsrelate
ngsrelate  -g angsdput.glf.gz -n 6 -f freq >resi

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 of with two samples

Pair	k0	k1	k2	loglh	nIter	coverage
(0,1)	0.673213	0.326774	0.000013	-1710940.769941	19	0.814658

Example of output with 6 samples:

cat resi
Pair	k0	k1	k2	loglh	nIter	coverage
(0,1)	0.675337	0.322079	0.002584	-1710946.832375	10	0.813930
(0,2)	0.458841	0.526377	0.014782	-1666215.528333	10	0.808822
(0,3)	1.000000	0.000000	0.000000	-1743992.363193	-1	0.816266
(0,4)	1.000000	0.000000	0.000000	-1759202.971213	-1	0.818856
(0,5)	1.000000	0.000000	0.000000	-1550475.615322	-1	0.752663
(1,2)	0.007111	0.991020	0.001868	-1580995.130867	10	0.806912
(1,3)	1.000000	0.000000	0.000000	-1728859.988212	-1	0.814272
(1,4)	1.000001	-0.000001	0.000000	-1744055.203870	9	0.816887
(1,5)	1.000000	0.000000	0.000000	-1536858.187440	-1	0.750917
(2,3)	1.000000	0.000000	0.000000	-1705157.832621	-1	0.809297
(2,4)	1.000000	0.000000	0.000000	-1719681.338365	-1	0.811804
(2,5)	1.000000	0.000000	0.000000	-1517388.260612	-1	0.746903
(3,4)	0.547602	0.439423	0.012975	-1743899.789842	10	0.819276
(3,5)	0.265819	0.482953	0.251228	-1467343.087647	10	0.754637
(4,5)	0.004655	0.995345	-0.000000	-1473415.049411	8	0.755734

The first column contain the individuals that was used for the analysis . The next three columns are the estimated relatedness coefficient. The fifth column is the log of the likelihood of the MLE. The sixth column is the number of iterations required to find the MLE, and finally the seventh column is fraction of non-missing sites, i.e. the fraction of sites where data was available for both individuals, and the minor allele frequency (MAF) above the threshold (default is 0.05 but may also user specified).

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