PCA MDS

single read sampling approach for PCA or MDS

This function is new and works from version 0.912 and in the latest developmental version from github

Brief Overview

./angsd -doIBS
	-> angsd version: 0.911-26-gf1cb0e0-dirty (htslib: 1.3-1-gc72ae90) build(Apr 27 2016 11:15:33)
	-> Analysis helpbox/synopsis information:
	-> Command: 
../angsd/angsd -doIBS 	-> Wed Apr 27 12:38:35 2016
--------------
abcIBS.cpp:
	-doIBS	0
	(Sampling strategies)
	 0:	 no IBS 
	 1:	 (Sample single base)
	 2:	 (Concensus base)
	-doCounts	0	Must choose -doCount 1
Optional
	-minMinor	0	Minimum observed minor alleles
	-minFreq	0.000	Minimum minor allele frequency
	-output01	0	output 0 and 1s instead of based
	-maxMis		-1	Maximum missing bases (per site)
	-doMajorMinor	0	use input files or data to select major and minor alleles
	-makeMatrix	0	print out the ibs matrix 
	-doCov		0	print out the cov matrix 

Options

-doIBS [int]

Print a single base from each individual at each position. 1: random sampled read. 2: Consensus base

doCounts [int]

Method requeres counting the different bases at each position. Therefore, -doCounts 1 must be used

-doMajorMinor [int]

The covariance matrix can only be calculated for diallelic sites. Therefore, choose a methods for selecting the major and minor allele (see Inferring_Major_and_Minor_alleles). This can also be use if you only want to make this assumption for the IBS matrix or only want to print out bases that are either the major or minor.

-minMinor [int]

Minimum observed minor alleles. The default in 0. If you do not use -doMajorMinor then the number of minor alleles are the sum of the 3 most uncommon alleles.

--minFreq [float]

Minimum minor allele frequency. The default in 0. If you do not use -doMajorMinor then the frequency is the sum of the frequencies of the 3 most uncommon alleles.

-output01 [int]

output 0 and 1s instead of base -maxMis -1 Maximum missing bases (per site) -doMajorMinor 0 use input files or data to select major and minor alleles -makeMatrix 0 print out the ibs matrix -doCov 0 print out the cov matrix

Use as a filter

Sites with a p-value below the p-value threshold will be removed.

Output

This function will also print the results of the selected sites. If you choose -HWE_pval 1 then all sites (that pass other filters) will be outputted.

Example of output *.hwe.gz

Chromo  Position        Major   Minor   hweFreq Freq    F       LRT     p-value
1       14000873        G       A       0.282473        0.263594        0.674624        3.140936e+00    7.634997e-02
1       14015890        A       G       0.283119        0.300032        0.999762        8.207572e+00    4.171594e-03
1       14018430        A       C       0.276112        0.299817        0.675018        2.780118e+00    9.544113e-02
1       14033343        A       G       0.295368        0.299442        0.999762        6.473824e+00    1.094747e-02
1       14037881        T       A       0.306003        0.341598        -0.518384       3.178415e+00    7.461710e-02
1       14038946        T       C       0.329113        0.333424        0.999775        6.925424e+00    8.497884e-03

Chromo is the chromosome

Position is the position Major is the major allele

Minor is the minor allele

hweFreq is the allele frequency assuming HWE (same as -doMaf 1)

Freq is the allele frequency without HWE assumption

F is the scale departure from HWE (inbreeding coefficient - see model)

LRT is the likelihood ratio statistic

p-value is the p-value based on a likelihood ratio test

Model

Probability of genotypes without assumption of HWE

${\begin{aligned}p(G=0|f,F)&=(1-f)^{2}+f(1-f)F\\p(G=1|f,F)&=2f(1-f)-2f(1-f)F\\p(G=2|f,F)&=f^{2}+f(1-f)F\end{aligned}}$

n

total number of individuals

X

all sequencing data for a site

f

allele frequency

F

inbreeding coefficient*

G

true unobserved genotype

total likelihood $p(X|f,F)\sim \prod _{i}^{n}p(X_{i}|f,F)=\prod _{i}^{n}\sum _{G\in \{0,1,2\}}p(X_{i}|G)p(G|f,F)$

• NB! we allow for negative values of F in order to be able to detect any divination from HWE.