NgsAdmixTutorial

-Example NGSadmix - Simple-

In our first example, we will be using a small dataset with low depth NGS data from 30 human samples: 10 from Nigeria (YRI), 10 from Japan (JPT) and 10 with European Ancestry (CEU).

Set directories to all required programs and the data you will use depending on where you installed them every time you open a new terminal window

1. Set path to NGSadmix

NGSADMIX=~/Software/NGSadmix

1. test the link

ls $NGSADMIX

1. Set path to the directory with the input files

AA=/../home/albrecht/PhDCourse

1. test the link

ls $AA To create the data files, please go the the following link: https://github.com/mfumagalli/ngsTools/blob/master/Scripts/data.sh

Create the directories that will be used for working: mkdir Demo cd Demo mkdir Data mkdir Results

1. Set paths to local directories

IN_DIR=~/Demo/Data OUT_DIR=~/Demo/Results

#Test the links ls $IN_DIR ls $OUT_DIR

NGSadmix uses Genotype Likelihoods (GLs) in .beagle format as input. The input file has been created for you. A file with labels that indicate which population the individuals are sampled from is also provided as the population information. Copy the files to your input folder ($IN_DIR): cp xxxx $IN_DIR cp $AA/admixture/data/pop.info $IN_DIR

CEU Europeans (mostly of British ancestry) JPT East Asian - Japanese individuals YRI West African - Nigerian Yoruba individuals

We will use a very reduced data set: 10 individuals from each population a very reduced genome 30 x 100k random regions across the autosomes Each individual is sequenced at 2-6X Aim: To infer admixture proportions for low depth sequencing data

We need to prepare the population information file by cutting the first column, sorting and counting: cut -f 1 -d " " $IN_DIR/pop.info | sort | uniq -c

Now let’s analyze the input file:

In general, the first three columns of a beagle file contain marker name and the two alleles, allele1 and allele2, present in the locus (in beagle A=0, C=1, G=2, T=3). All following columns contain genotype likelihoods (three columns for each individual: first GL for homozygote for allele1, then GL for heterozygote and then GL for homozygote for allele2). Note that the GL values sum to one per site for each individual. This is just a normalization of the genotype likelihoods in order to avoid underflow problems in the beagle software, but it does not mean that they are genotype probabilities.

In order to see the first 10 columns and 10 lines of the input file, type: gunzip -c $IN_DIR/Demo1GLs | head -n 10 | cut -fl-10 | column -t

Use this command to count the number of lines of the input file. The number of lines, indicates the number of loci for which there are GLs plus one (as the command includes the count of the header line): gunzip -c $IN_DIR/Demo1GLs | wc -l

To run an analysis of the GLs with NGSadmix, assuming the number of ancestral populations is K=3, type the following command:

$NGSadmix -likes $IN_DIR/Demo1GLs.beagle.gz -K 3 -minMaf 0.05 -seed 1 -o $OUT_DIR/Demo1NGSadmix

The output:

The analysis performed by NGSadmix produces 4 files:

Log likelihood of the estimates A .log file that summarizes the run. Let’s take a look at the log file to determine the log likelihood of the estimates achieved by NGSadmix which is called the “best like” in the file: cat Demo1NGSadmix.log

Estimated allele frequency A zipped .fopt file, that contains an estimate of the allele frequency in each of the 3 assumed ancestral populations (there is a line for each locus). We can use this file to obtain the estimated allele frequency of the first 5 SNPs (one per line) of the three assumed ancestral populations, by typing the following command: zcat Demo1NGSadmix.fopt.gz | head -n 5

Estimated admixture proportions A .qopt file, that contains an estimate of the individual's ancestry proportion from each of the three assumed ancestral populations (there is a line for each individual). To obtain the estimated admixture proportions for the first 5 individuals, type the following command: head -n 5 Demo1NGSadmix.qopt

DemoNGSadmix.filter: if the filter was used, it will show the sites that were left out. If the filter is used, it will show the sites that were left out or in… CHECK

Follow these instructions to make a simple plot of the estimated admixture proportions for all individuals in R:

Type “R” in the terminal and press enter. Paste the following code into R:

1. set up the working directories

1. Fill up a table with the IDs of the population information for each individual

pop<-read.table("pop.info", as.is=T)

1. Read inferred admixture proportions

q<-read.table("Demo1NGSadmix.qopt")

1. Plot them (ordered by population)

ord = order(pop) par(mar=c(7,4,1,1)) barplot(t(q)[,ord],col=c(2,1,3),names=pop[ord],las=2,ylab="Admixture proportions",cex.names=0.75)

The y-axis of the plot show the admixture proportions and the individuals in the samples are plotted in the x-axis. Each color represents a different ancestral population. The proportion of each color shows the different admixture of the individuals for each ancestral population. The plot is sorted by the population of origin of each individual in the sample, and therefore, it shows blocks with prevalence of a certain color, which represents the population to which each individual belongs.

NB As you could tell from the number of loci included in the analysis, the above analysis is based on data from very few loci (actually we on purpose only analyzed data from a small part of the genome to make sure the analysis ran fast). Results from an analysis of data from the entire genome can be seen here.