ANGSD: Analysis of next generation Sequencing Data

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If you do not have population allele frequencies the you cannot estimate kinship coefficients. However, you can still make some claims about the relationship of your samples based on IBS patterns.
If you do not have population allele frequencies the you cannot estimate kinship coefficients. However, you can still make some claims about the relationship of your samples based on IBS patterns.
{| class="wikitable" style="text-align: center
!|  ind1 below, ind2 -> || <math>G=0 </math> || <math>G=1 </math>  ||<math>G=2 </math>
|-
|  <math>G=0 </math>    ||    <math>0 </math>    ||    <math>1</math>  ||  <math>0 </math>
|-
|  <math>G=1 </math>  || <math>0.25  </math>    ||  <math>  0.5  </math>  ||  <math> 0.25 </math>
|-
|  <math>G=2 </math>  || <math> 0.5  </math>  ||    <math>0.5 </math> ||  <math> 0 </math>
|}

Revision as of 14:55, 12 July 2016

NGSrelate - estimation of IBD probabilities

In order to estimate kinship coefficient then population allele frequencies are needed. These can be estimated from data if you can multiple individuals. For some individuals, for example most human populations, there are publicly available data. If you can obtain population allele frequencies or have a many samples from your population then we recommend that you use NGSrelate has works with ANGSD output. From the estimated IBD probabilities you can then infer the relationship. Below is a table of the expected IBD sharing probabilities assuming no inbreeding


Relationship
Parent-Offspring
Full siblings
Half siblings
First cousins


NGSrelate has its very own website http://www.popgen.dk/software/index.php/NgsRelate


IBS/genotype distribution

If you do not have population allele frequencies the you cannot estimate kinship coefficients. However, you can still make some claims about the relationship of your samples based on IBS patterns.


ind1 below, ind2 ->