• No results found

429

Aguilar, I., I. Misztal, D.L. Johnson, A. Legarra, S. Tsuruta, and T.J. Lawlor. 2010. Hot topic:

430

A unified approach to utilize phenotypic, full pedigree, and genomic information for

431

genetic evaluation of Holstein final score. J. Dairy Sci. 93:743–752.

432

Bradford, H. l., I. Pocrnić, B. o. Fragomeni, D. a. l. Lourenco, and I. Misztal. 2017. Selection

433

of core animals in the Algorithm for Proven and Young using a simulation model. J.

434

Anim. Breed. Genet. 134:545–552. doi:10.1111/jbg.12276.

435

Calus, M.P.L., and J. Vandenplas. 2016. Calc_grm – a Program to Compute Pedigree,

436

Genomic, and Combined Relationship Matrices. ABGC, Wageningen UR Livestock

437

Research.

438

Christensen, O.F. 2012. Compatibility of pedigree-based and marker-based relationship

439

matrices for single-step genetic evaluation. Genet. Sel. Evol. 44:37.

440

Christensen, O.F., and M.S. Lund. 2010. Genomic prediction when some animals are not

441

genotyped. Genet. Sel. Evol. 42:2.

442

Fernando, R.L., H. Cheng, and D.J. Garrick. 2016. An efficient exact method to obtain

443

GBLUP and single-step GBLUP when the genomic relationship matrix is singular.

444

Genet. Sel. Evol. 48:80. doi:10.1186/s12711-016-0260-7.

445

Fragomeni, B.O., D.A.L. Lourenco, S. Tsuruta, Y. Masuda, I. Aguilar, A. Legarra, T.J.

446

Lawlor, and I. Misztal. 2015. Hot topic: Use of genomic recursions in single-step

447

genomic best linear unbiased predictor (BLUP) with a large number of genotypes. J.

448

Dairy Sci. 98:4090–4094.

449

Golub, G., and C.F. Van Loan. 1996. Matrix Computations. third ed. Johns Hopkins

450

University Press, Baltimore, MD, USA.

451

Hill, W.G., and A. Robertson. 1968. Linkage disequilibrium in finite populations. Theor.

452

Appl. Genet. 38:226–231. doi:10.1007/BF01245622.

453

Ibánẽz-Escriche, N., R.L. Fernando, A. Toosi, and J.C. Dekkers. 2009. Genomic selection of

454

purebreds for crossbred performance. Genet. Sel. Evol. 41:12.

doi:10.1186/1297-455

9686-41-12.

456

Legarra, A., O.F. Christensen, I. Aguilar, and I. Misztal. 2014. Single Step, a general

457

approach for genomic selection. Livest. Sci. 166:54–65.

458

Lourenco, D.A.L., S. Tsuruta, B.O. Fragomeni, C.Y. Chen, W.O. Herring, and I. Misztal.

459

2016. Crossbreed evaluations in single-step genomic best linear unbiased predictor

460

using adjusted realized relationship matrices. J. Anim. Sci. 94:909–19.

461

doi:10.2527/jas.2015-9748.

462

Lourenco, D.A.L., S. Tsuruta, B.O. Fragomeni, Y. Masuda, I. Aguilar, A. Legarra, J.K.

463

Bertrand, T.S. Amen, L. Wang, D.W. Moser, and I. Misztal. 2015. Genetic evaluation

464

using single-step genomic best linear unbiased predictor in American Angus. J. Anim.

465

Sci. 93:2653–2662. doi:10.2527/jas.2014-8836.

466

Mäntysaari, E.A., R.D. Evans, and I. Strandén. 2017. Efficient single-step genomic evaluation

467

for a multibreed beef cattle population having many genotyped animals. J. Anim. Sci.

468

95:4728–4737. doi:10.2527/jas2017.1912.

469

Masuda, Y., I. Misztal, S. Tsuruta, A. Legarra, I. Aguilar, D.A.L. Lourenco, B.O. Fragomeni,

470

and T.J. Lawlor. 2016. Implementation of genomic recursions in single-step genomic

471

best linear unbiased predictor for US Holsteins with a large number of genotyped

472

animals. J. Dairy Sci. 99:1968–1974. doi:10.3168/jds.2015-10540.

473

Misztal, I. 2016. Inexpensive computation of the inverse of the genomic relationship matrix in

474

populations with small effective population size. Genetics 202:401–409.

475

Misztal, I., A. Legarra, and I. Aguilar. 2014. Using recursion to compute the inverse of the

476

genomic relationship matrix. J. Dairy Sci. 97:3943–3952.

477

Mrode, R.A. 2005. Linear Models for the Prediction of Animal Breeding Values. 2nd ed.

478

CABI Publishing, Wallingford, UK.

479

ten Napel, J., M.P.L. Calus, M. Lidauer, I. Stradén, E.A. Mäntysaari, H.A. Mulder, and R.F.

480

Veerkamp. 2016. MiXBLUP, User-Friendly Software for Large Genetic Evaluations

481

Systems. Version 2.0. Wageningen, the Netherlands.

482

Ostersen, T., O.F. Christensen, P. Madsen, and M. Henryon. 2016. Sparse single-step method

483

for genomic evaluation in pigs. Genet. Sel. Evol. 48:48.

doi:10.1186/s12711-016-484

0227-8.

485

Pocrnic, I., D.A.L. Lourenco, Y. Masuda, A. Legarra, and I. Misztal. 2016a. The

486

dimensionality of genomic information and its effect on genomic prediction. Genetics

487

203:573–581.

488

Pocrnic, I., D.A.L. Lourenco, Y. Masuda, and I. Misztal. 2016b. Dimensionality of genomic

489

information and performance of the Algorithm for Proven and Young for different

490

livestock species. Genet. Sel. Evol. 48:82. doi:10.1186/s12711-016-0261-6.

491

Powell, J.E., P.M. Visscher, and M.E. Goddard. 2010. Reconciling the analysis of IBD and

492

IBS in complex trait studies. Nat. Rev. Genet. 11:800–805. doi:10.1038/nrg2865.

493

Raymond, M., and F. Rousset. 1995. GENEPOP (Version 1.2): Population genetics software

494

for exact tests and ecumenicism. J. Hered. 86:248–249.

495

Rousset, F. 2008. genepop’007: a complete re-implementation of the genepop software for

496

Windows and Linux. Mol. Ecol. Resour. 8:103–106.

doi:10.1111/j.1471-497

8286.2007.01931.x.

498

Sargolzaei, M., and F.S. Schenkel. 2009. QMSim: a large-scale genome simulator for

499

livestock. Bioinformatics 25:680–681.

500

Strandén, I., K. Matilainen, G.P. Aamand, and E.A. Mäntysaari. 2017. Solving efficiently

501

large single-step genomic best linear unbiased prediction models. J. Anim. Breed.

502

Genet. 134:264–274. doi:10.1111/jbg.12257.

503

Tukey, J.W. 1949. Comparing individual means in the analysis of variance. Biometrics 5:99–

504

114.

505

Vitezica, Z.G., I. Aguilar, I. Misztal, and A. Legarra. 2011. Bias in genomic predictions for

506

populations under selection. Genet. Res. 93:357–366.

507

Welch, B.L. 1947. THE GENERALIZATION OF “STUDENT”S’ PROBLEM WHEN

508

SEVERAL DIFFERENT POPULATION VARLANCES ARE INVOLVED.

509

Biometrika 34:28–35. doi:10.1093/biomet/34.1-2.28.

510

Wientjes, Y.C.J., and M.P.L. Calus. 2017. BOARD INVITED REVIEW: The

purebred-511

crossbred correlation in pigs: A review of theory, estimates, and implications. J. Anim.

512

Sci. 95:3467–3478.

513

514

515

E-Supplements

516

Table S1 Number of purebred and crossbred animals with a phenotype per generation

517

(average for the 5 replicates; SD within brackets).

518

519

Table S2 Number of purebred and crossbred animals with a phenotype and a genotype per

520

generation (average for the 5 replicates; SD within brackets).

521

522

Table S3. Relative accuracies (average for the 5 replicates; SD within brackets) of GEBV

523

from alternative core groups for the purebred (PB) and crossbred (CB) performance for

524

genotyped selection candidates.

525

526

Table S4. Pearson correlations (average for the 5 replicates; SD within brackets) between

527

GEBV for genotyped selection candidates from alternative core groups1 and GEBV from the

528

direct inversion of G.

529

530

Table S5. Regression coefficients (average for the 5 replicates; SD within brackets) of TBV

531

on GEBV from alternative core groups and the direct inversion of G for genotyped selection

532

candidates.

533

534

Table S6. Relative mean squares errors (average for the 5 replicates; SD within brackets) of

535

GEBV from alternative core groups for genotyped selection candidates.

536

537

Figures

538 539

540

Figure 2.

541

542

543

Figure 3.

544

545

546

Figure 4.

547

548

549

Figure 5.

550

551

552

Figure 6.

553

554

Figure 1. Schematic representation of the simulation. The crossbreeding program started at

555

generation 200 (generation numbers in bold). The number of males (M) and females (F) per

556

generation and per breed (A, B, and C), or per cross (BC, and A(BC)), are reported within

557

brackets. Blue arrows denote the sires and dams of the next generation; red arrows denote the

558

dams of the next generation; green arrows denote the sires of the next generation.

559

560

Figure 2. Projections of genomic relationships for purebred (A, B, and C) and crossbred (BC

561

and A(BC)) genotyped animals into the two first eigenvectors for the first replicate.

562

563

Figure 3. Proportions of core animals per generation and breed composition of one replicate

564

for the scenario using 8,000 core animals. Core animals were selected using four different

565

strategies: 1) only from breed A animals (Breed A), 2) from purebred animals of breed A, B

566

and C (PB), 3) from purebred animals of breed A, B and C, and crossbred BC and A(BC)

567

animals (PB + CB), and (4) chosen based on a QR decomposition of the genotype matrix

568

(QR). Darker colours represent higher proportions of core animals per generation and breed

569

composition.

570

571

Figure 4. Relative correlations of GEBV from different sizes of core groups with only breed

572

A animals. Relative correlations for the purebred performance (PP) and crossbred

573

performance (CP) traits are defined as the ratio between the accuracies of GEBV from

574

alternative core groups and the corresponding accuracies of GEBV from 𝐆𝑑𝑖𝑟𝑒𝑐𝑡−1 . Vertical

575

columns depict the number of eigenvalues that explained 98% and 99% of the variation in 𝐆.

576

Results are averages for the 5 replicates.

577

578

579

Figure 5. Relative correlations of GEBV from alternative core groups for the purebred

580

performance traits. Core groups include randomly selected purebred and crossbred animals

581

(Purebred + Crossbred core), randomly selected purebred animals (Purebred core), and

582

animals selected based on a QR decomposition of the genotype matrix (QR core). Relative

583

correlations are defined as the ratio between the accuracies of GEBV from alternative core

584

groups and the corresponding accuracies of GEBV from 𝐆𝑑𝑖𝑟𝑒𝑐𝑡−1 . Vertical columns depict the

585

number of eigenvalues that explained 98% and 99% of the variation in 𝐆. Results are

586

averages for the 5 replicates.

587

588

Figure 6. Relative correlations of GEBV from alternative core groups for the crossbred

589

performance trait. Core groups include randomly selected purebred and crossbred animals

590

(Purebred + Crossbred core), randomly selected purebred animals (Purebred core), and

591

animals selected based on a QR decomposition of the genotype matrix (QR core). Relative

592

correlations are defined as the ratio between the accuracies of GEBV from alternative core

593

groups and the corresponding accuracies of GEBV from 𝐆𝑑𝑖𝑟𝑒𝑐𝑡−1 . Vertical columns depict the

594

number of eigenvalues that explained 98% and 99% of the variation in 𝐆. Results are

595

averages for the 5 replicates.

596

597

Tables

598

Table 1. Heritabilities (diagonal) and genetic correlations (off-diagonal) among the five

599

simulated traits.

600

Trait Purebred A Purebred B Purebred C Crossbred BC Crossbred A(BC) Purebred A 0.28

Purebred B 0.46 0.39

Purebred C 0.27 0.80 0.22

Crossbred BC 0.33 0.58 0.30 0.36

Crossbred A(BC) 0.55 0.31 0.26 0.69 0.23

601

Table 2. Accuracies, bias, and mean square errors (MSE) of GEBV from the direct inversion

602

of 𝐆 (average for the 5 replicates; SD within brackets).

603

Selection candidates

Number Purebred performance Crossbred performance Accuracy Bias MSE Accuracy Bias MSE

Breed A 5010

(24)

0.81 (0.02)

1.04 (0.05)

1.11 (0.69)

0.68 (0.04)

0.98 (0.08)

0.68 (0.51)

Breed B 4975

(30)

0.85 (0.01)

1.06 (0.03)

1.16 (0.81)

0.63 (0.02)

0.95 (0.04)

0.90 (0.43)

Breed C 5016

(45)

0.79 (0.04)

1.04 (0.03)

1.42 (0.74)

0.71 (0.04)

1.04 (0.07)

1.35 (1.18) 604

Table 3. Regression coefficients (average for the 5 replicates; SD within brackets) of TBV on

605

GEBV from alternative core groups1 for genotyped selection candidates.

606

Number of core animals

Purebred performance Crossbred performance Breed

A

PB PB+CB QR Breed

A

PB PB+CB QR

Breed A selection candidates

4000 1.04 Breed B selection candidates

4000 1.49 Breed C selection candidates

4000 1.69

1 Core groups include 1) randomly selected breed A animals only (Breed A), 2) randomly selected purebred 607

animals (PB), 3) randomly selected purebred and crossbred animals (PB+CB), and 4) animals selected based on 608

a QR decomposition of the genotype matrix (QR).

609 610

Table 4. Relative mean squares errors1 (average for the 5 replicates; SD within brackets) of

611

GEBV from alternative core groups2 for genotyped selection candidates.

612

Number of core animals

Purebred performance Crossbred performance Breed

A

PB PB+CB QR Breed

A

PB PB+CB QR

Breed A selection candidates

4000 1.09 Breed B selection candidates

4000 1.75 Breed C selection candidates

4000 1.29

1 Results are expressed as the ratio between MSE of GEBV from alternative core groups and MSE of GEBV 613

from the direct inversion of 𝐆.

614

2 Core groups include 1) randomly selected breed A animals only (Breed A), 2) randomly selected purebred 615

animals (PB), 3) randomly selected purebred and crossbred animals (PB+CB), and 4) animals selected based on 616

a QR decomposition of the genotype matrix (QR).

617 618

619

Table 5. Quality of GEBV using APY for the core and non-core selection candidates. 1 620

Selection candidates

Number Purebred performance Crossbred performance Accuracy2 Reg.

coef.

1 Results (average for the 5 replicates; SD within brackets) are shown for the scenario using 8000 core animals 621

randomly selected among purebred and crossbred animals.

622

2 Results for accuracies and mean square errors (MSE) are expressed as the ratio between accuracies (MSE) of 623

GEBV using APY and accuracies (MSE) of GEBV using the direct inversion of 𝐆.

624 625

Related documents