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Table 1 Model learned from the T1D data set. Model learned from the T1D data set using 1-e5 as the p-value threshold, the holdout approach, AdaBoostM1 as the learning algorithm with default configuration (decision stump as the weak learning algorithm and 10 iterations)

From: A comparison of genomic profiles of complex diseases under different models

Chr

Chr

SNP

Allele

Allele

Weight

Genotypes

Weight

Genotypes

#

Pos

 

1

2

rule 1

rule 1

rule 2

rule 2

1

77051324

SNP_A−1827111

A

C

0.0801

{0, missing}

  

6

32444658

SNP_A−1934589

A

G

0.2326

{0}

  

6

30135583

SNP_A−2111335

A

G

0.2171

{0}

0.0543

{1}

6

31395153

SNP_A−2079423

C

T

0.1525

{0,1}

  

6

30390814

SNP_A−2222387

A

G

0.0672

{0,1}

  

6

31112694

SNP_A−4293786

C

T

0.0517

{0,1}

  

19

39266932

SNP_A−4281637

A

G

0.0904

{0,1}

  
  1. Weights and genotypes values are referred to class 1, i.e. absence of disease. Chromosome positions correspond to assembly NCBI dbSNP GRCh38.p2