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A recursive method of approximation of the inverse of genomic relationship matrix

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A recursive method of

approximation of the inverse of

genomic relationship matrix

P. Faux *,1, I. Misztal2, N. Gengler 1,3

1University of Liège, Gembloux Agro-Bio Tech, Belgium 2University of Georgia, Animal and Dairy Science, Athens GA

3National Fund for Scientific Research, Brussels, Belgium

2011 ADSA-ASAS Joint Annual Meeting New Orleans, LA, July 10-14

* Supported by the National

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Introduction

Inverse of genomic relationship matrix (G)

useful in different genomic evaluations:

single-step, multiple-steps

Inversion becomes time-consuming when

number of genotyped animals >50,000

A good approximation of G inverse will

become useful

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Methods: Approximated

inverse of G

Decomposition of A-1:

A

-1

=(T

-1

)’ . D

-1

. T

-1

We assume the following model for G-1:

G

-1

=(T*)’ . (D

-1

)* . T* + E

Or,

(G

-1

)*=(T*)’ . (D

-1

)* . T*

2 approximations have to be done: T* and (D-1)*

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Methods: Case of A

-1

Animal a, of sire s and dam d:

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

s ... d ... a ... s ... d ... a ... 1 1 1 1 -.5 -.5 1 1 A T-1 s ... d ... a ... s ... d ... a ... -.5 -.5

A

x

= -

b

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Methods: Case of G

-1

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

s ... d ... a ... s ... d ... a ... 1 1 1 1 1 1 G T* s ... d ... a ... s ... d ... a ...

 = -

x

b

A

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Methods: Case of G

-1

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

s j d ... a ... s j d ... a ... 1 1 1 1 1 1 G T* s j d ... a ... s j d ... a ...

 = -

x

b

A

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Methods: Approximation of

D

-1

(G

-1

)*=(T*)’ . (D

-1

)* . T*

D = T* . G

. (T*)’

D close to diagonal  2 options:

1. Invert only diagonal elements  (D-1)* is a diagonal

matrix

2. Apply the same rules as for approximation of G-1 but

for D-1  (D-1)* is a sparse matrix

(D

-1

)*=(T

2

*)’ . (D

2-1

)

* . T

2

*

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Methods: Recursive

approximation

Same recursion may be repeated n times on the “remaining D”

(G

-1

)*

n

=(T*

1

)’ . ... . (T*

n

)’ . (D

n-1

)* . T*

n

. ... . T*

1 • At each round, new threshold p

2 computational bottle-necks are shown in this equation

Algorithm may be implemented in different ways

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Examples: Material

Dairy bulls data set:

1,718 genotyped bulls

38,416 SNP

Single-step genomic evaluations on Final Score, each evaluation uses a different (G-1)*

Construction of G:

G=ZZ’/d

Both diagonals and off-diagonals of G centered on A22

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Examples: Quality of

approximation

Mean square difference (MSD) between G-1 and (G-1)*

MSD between G-1 and A

22-1: 81.49*10-4

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

Round p MSD 1 0.21 66.53 * 10-4 2 0.017 34.87 * 10-4 3 0.009 16.81 * 10-4 4 0.005 5.97 * 10-4 5 0.003 1.82 * 10-4

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Examples: Incidence on

evaluation

Correlations r between EBV for genotyped animals

r between G-1 and A

22-1: 0.76

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

Round p r 1 0.21 0.79 2 0.017 0.91 3 0.009 0.97 4 0.005 0.99 5 0.003 1.00

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Examples: Sparsity

Percentage of zeros in lower off-diagonal part of Tf

2011 ADSA-ASAS Joint Annual Meeting, New Orleans, July 10-14

Round p % of 0 1 0.21 92.35 2 0.017 10.78 3 0.009 2.28 4 0.005 0.86 5 0.003 0.49

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Examples: Others results

Use of this algorithm to compute (A

22-1

)*

Closeness with A

22-1

: from 2*10

-4

to 3*10

-5

No incidence on evaluations after 3 rounds

93% of 0 after 1 round, ... up to ~80%

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Discussion

Consumption of time

Savings on both bottle-necks

Might be interesting in some cases

Construction of consistent relationships and

covariances

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Acknowledgements

Animal and Dairy Science (ADS) Department of University of Georgia (UGA), for hosting and

advising (Mrs H. Wang, Dr S. Tsuruta, Dr I. Aguilar) • Animal Breeding and Genetics Group of Animal

Science Unit of Gembloux Agro-Bio Tech of University of Liège (ULg – Gx ABT)

Holstein Association USA Inc. for providing data

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