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Table 1 Power and Type I error rates for gene by methylation interactions

From: Longitudinal data methods for evaluating genome-by-epigenome interactions in families

Model

Outcome

Nominal (p < 0.05)

Genome-wide (p < 1.08 × 10− 7)

1 (0.125)

8 (0.10)

6 (0.075)

17 (0.05)

10 (0.025)

Type I error

1 (0.125)

8 (0.10)

6 (0.075)

17 (0.05)

10 (0.025)

Type I error

LME

Pre/Post

0.930

0.790

0.690

0.545

0.290

0.048

0.016

0.020

0.000

0.000

0.000

0.000

Change

0.839

0.715

0.595

0.510

0.210

0.038

0.011

0.005

0.000

0.000

0.000

0.000

GEE

Pre/Post

0.935

0.835

0.705

0.555

0.290

0.073

0.022

0.025

0.005

0.000

0.000

0.002

Change

0.855

0.735

0.565

0.535

0.240

0.069

0.016

0.005

0.000

0.000

0.000

0.001

GEE–BC

Pre/Post

0.914

0.835

0.630

0.530

0.265

0.051

0.011

0.015

0.000

0.000

0.000

0.001

Change

0.828

0.715

0.540

0.500

0.210

0.052

0.011

0.005

0.000

0.000

0.000

0.001

QIF

Pre/Post

0.941

0.845

0.685

0.580

0.410

0.120

0.054

0.055

0.015

0.000

0.005

0.002

Change

0.860

0.735

0.575

0.580

0.345

0.111

0.048

0.015

0.000

0.000

0.000

0.002

QIF–BC

Pre/Post

0.882

0.760

0.520

0.460

0.205

0.043

0.005

0.010

0.000

0.000

0.000

0.000

Change

0.780

0.670

0.450

0.450

0.180

0.042

0.005

0.005

0.000

0.000

0.000

0.000

  1. BC, Bias-corrected methods; Change, post-pre change triglyceride score as the outcome; GEE, generalized estimating equations; LME, linear mixed effects; Pre/Post, posttreatment triglyceride as the outcome and pretreatment as a baseline covariate; QIF, quadratic inference functions
  2. The proportion of 200 (or 186 in the case of the chromosome 1 site) replicates that each SNP × CpG interaction was identified as significant for each significance threshold. Presented is the chromosome location with simulated expected heritability (hg2) in parentheses
  3. Causal chromosome sites simulated include: Chr 1 (SNP: rs9661059; CpG: cg00000363); Chr 8 (SNP: rs1012116; CpG: cg18772399); Chr 6 (SNP: rs736004; CpG: cg10480950); Chr 17 (SNP: rs4399565; CpG: cg01242676); and Chr 10 (SNP: rs10828412; CpG: cg00045910)