In amandaforde/winnerscurse: Winner's Curse Adjustment Methods for Summary Statistics from Genome-Wide Association Studies

knitr::opts_chunk$set(
  collapse = TRUE,
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library(winnerscurse)

Our R package, winnerscurse, also contains several functions which have the ability to obtain more accurate SNP-trait association estimates when the summary statistics from two genetic association studies, namely the discovery and replication GWASs, are available. Thus, this second vignette demonstrates how the package can be used to obtain new adjusted association estimates for each SNP using these two data sets. Similar to the first vignette which focused on 'discovery only' methods, we first use the function sim_stats to create two toy data sets and then, illustrate how a user may employ the package's functions to adjust for the bias imposed by Winner's Curse.

The methods that are currently available for implementation include:

1. Conditional Likelihood method - adapted from Zhong and Prentice (2008)
2. UMVCUE method - Bowden and Dudbridge (2009)

It is important to note that with both of these methods, adjustments are only made to SNPs that are deemed significant in the discovery data set, i.e. the $p$-values in the discovery data set of these SNPs are less than that of the specified threshold, $\alpha$.

A third method has also been added which obtains a new association estimate for each significant SNP in the discovery data set using a combination of the discovery and replication estimates:

1. MSE minimization method - based on Ferguson et al. (2017)

Creating two toy data sets

• The function sim_stats allows users to simulate two data sets of GWAS summary statistics which are based on the same true underlying SNP-trait association values. This provides users with simulated discovery and replication GWAS summary statistics to which the aforementioned correction methods can then be applied.

• When considering obtaining a simulated set of summary statistics for both discovery and replication GWASs, sim_stats requires the user to specify six arguments, namely nsnp, h2, prop_effect, nid, rep and rep_nid. The first four arguments are defined just as in the first vignette, while rep and rep_nid are defined as follows:

• rep: a logical parameter, i.e. TRUE or FALSE, which allows the user to specify if they wish to simulate summary statistics for a replication GWAS as well

• rep_nid: the number of samples in the replication study

• In order to obtain summary statistics for a replication GWAS, the user must change rep from its default setting of rep=FALSE to rep=TRUE. It is noted that the default value for rep_nid is rep_nid=50000. Thus, if the default values are used in sim_stats for every argument except rep, two sets of summary statistics will be simulated for 1,000,000 independent SNPs in which 1% have a true effect on this trait with moderate heritability and a total of 50,000 individuals have been sampled in both the discovery and replication studies.

• As mentioned in the first vignette, sim_stats outputs a list with three components, true, disc and rep. When both discovery and replication GWASs are considered and the function parameter rep has been set to TRUE, the third element of this list will no longer be NULL. Instead, a data frame with three columns is outputted. Similar to disc, for each SNP, the rep data frame contains its ID number, its estimated effect size obtained in this replication study and associated standard error. We again note that this function outputs both sets of summary statistics in a suitable way so that the Winner's Curse correction methods can be directly applied, i.e. in the form of a data frame with three columns rsid, beta and se.

set.seed(1998)

sim_dataset <- sim_stats(nsnp=10^6,h2=0.4,prop_effect=0.01,nid=50000,rep=TRUE,rep_nid=50000)

## simulated discovery GWAS summary statistics
disc_stats <- sim_dataset$disc
head(disc_stats)

## simulated replication GWAS summary statistics
rep_stats <- sim_dataset$rep
head(rep_stats)

Method 1: Conditional Likelihood

• The function condlike_rep implements a version of the conditional likelihood method for obtaining bias-reduced association estimates described in Zhong and Prentice (2008).

• The function requires as inputs two independent data sets, one representing a discovery GWAS, summary_disc, and the other a replication study with identical SNPs, summary_rep, as well as a specification of the significance threshold, alpha, to be used. As before, the data sets must be in the form of data frames with columns rsid, beta and se, all columns of the data frames must contain numerical values and each row of both data frames must represent a unique SNP, identified by rsid. SNPs must be in the exact same order in both data sets, i.e. the identity summary_rep$rsid == summary_disc$rsid must evaluate to TRUE.

• Furthermore, the parameter conf_interval in condlike_rep provides the user with the option to obtain confidence intervals for each of the adjusted association estimates. The default setting is conf_interval=FALSE. Inserting conf_interval=TRUE when using the function will return three sets of lower and upper confidence interval boundaries for each SNP, each set corresponding to a particular form of adjusted estimate. The final parameter conf_level takes a numerical value between 0 and 1 which specifies the confidence interval, with the default being 0.95.

• In a similar manner to other functions included in the package, condlike_rep returns a single data frame with SNPs reordered based on significance. However, it only contains SNPs which have been deemed significant in the discovery data set. The first 5 columns of the data frame details the inputted information; rsid, beta_disc, se_disc, beta_rep, se_rep. Following this, beta_com is the inverse variance weighted estimate which is formally defined as:$$\hat\beta_{\text{com}} = \frac{\sigma_2^2 \hat\beta_1 + \sigma_1^2 \hat\beta_2}{\sigma_1^2 + \sigma_2^2},$$ in which $\hat\beta_1$ = beta_disc, $\hat\beta_2$ = beta_rep, $\sigma_1$ = se_disc and $\sigma_2$ = se_rep.

• The method implemented here uses just one selection cut-point at the first discovery stage as opposed to that described in Zhong and Prentice (2008) in which two separate selection thresholds are used. Thus, the maximum likelihood adjusted estimator, beta_MLE is defined to maximize the conditional likelihood at the observed $\hat\beta_{\text{com}}$:$$\hat\beta_{\text{MLE}} = \arg \max_{\beta} \log f(\hat\beta_{\text{com}}; \beta).$$ The conditional sampling distribution, $f(x;\beta)$ is approximated by: $$f(x;\beta) = \frac{\frac{1}{\sigma_{\text{com}}} \phi\left(\frac{x-\beta}{\sigma_{\text{com}}}\right) \cdot \left[\Phi\left(\frac{x-c\sigma_1}{\frac{\sigma_1}{\sigma_2}\sigma_{\text{com}}}\right) + \Phi\left(\frac{-x-c\sigma_1}{\frac{\sigma_1}{\sigma_2}\sigma_{\text{com}}}\right)\right]}{\Phi\left(\frac{\beta}{\sigma_1} - c\right) + \Phi\left(- \frac{\beta}{\sigma_1} - c\right)}.$$

• $c$ is the selection cut-point, i.e. all SNPs with $\mid \frac{\hat\beta_1}{\sigma_1}\mid \ge c$ are deemed as significant. The value of $c$ is easily obtained using the chosen alpha. In addition, $$\sigma^2_{\text{com}} = \frac{\sigma_1^2 \sigma_2^2}{\sigma_1^2 + \sigma_2^2}.$$

• Note that this function, $f(x;\beta)$ is slightly different from that given in the paper as only one selection cut-point is imposed here.

• Finally, Zhong and Prentice (2008) noted that simulation studies showed that $\hat\beta_{\text{com}}$ tended to have upward bias while $\hat\beta_{\text{MLE}}$ over-corrected and therefore, a combination of the two in the following form was proposed: $$\hat\beta_{\text{MSE}} = \frac{\hat\sigma^2_{\text{com}}\cdot \hat\beta_{\text{com}} + (\hat\beta_{\text{com}} - \hat\beta_{\text{MLE}})^2\cdot\hat\beta_{\text{MLE}}}{\sigma^2_{\text{com}}+(\hat\beta_{\text{com}} - \hat\beta_{\text{MLE}})^2}.$$ This $\hat\beta_{\text{MSE}}$ holds the final column of the outputted data frame in the default setting.

• The use of condlike_rep with our toy data sets in which conf_interval=FALSE is demonstrated below, with a significance threshold value of 5e-8:

out_CL <- condlike_rep(summary_disc=disc_stats, summary_rep=rep_stats, alpha=5e-8)
head(out_CL)

$~$

Confidence intervals:

• Firstly, the $(1-\alpha)\%$ confidence interval for $\hat\beta_{\text{com}}$ is simply calculated as: $$\hat\beta_{\text{com}} \pm \hat\sigma_{\text{com}}Z_{1-\frac{\alpha}{2}}.$$For $\hat\beta_{\text{MLE}}$, the profile confidence limits are the intersection of the log-likelihood curve with a horizontal line $\frac{\chi^2_{1,1-\alpha}}{2}$ units below its maximum. The MSE weighting method, as described above, can then be easily applied to the upper and lower boundaries of these two confidence intervals to obtain an appropriate confidence interval for $\hat\beta_{\text{MSE}}$. This gives: $$\hat\beta_{\text{MSE};\frac{\alpha}{2}} = \hat{K}{\frac{\alpha}{2}} \hat\beta{\text{com};\frac{\alpha}{2}} + \left(1-\hat{K}{\frac{\alpha}{2}}\right) \hat\beta{\text{MLE};\frac{\alpha}{2}}$$ $$\hat\beta_{\text{MSE};1-\frac{\alpha}{2}} = \hat{K}{1-\frac{\alpha}{2}} \hat\beta{\text{com};1-\frac{\alpha}{2}} + \left(1-\hat{K}{1-\frac{\alpha}{2}}\right) \hat\beta{\text{MLE};1-\frac{\alpha}{2}}$$ in which $\hat{K}{\frac{\alpha}{2}} = \frac{\hat\sigma^2{\text{com}}}{\hat\sigma^2_{\text{com}} + \left(\hat\beta_{\text{com};\frac{\alpha}{2}} - \hat\beta_{\text{MLE};\frac{\alpha}{2}}\right)^2} \;$ and $\; \hat{K}{1-\frac{\alpha}{2}} = \frac{\hat\sigma^2{\text{com}}}{\hat\sigma^2_{\text{com}} + \left(\hat\beta_{\text{com};1-\frac{\alpha}{2}} - \hat\beta_{\text{MLE};1-\frac{\alpha}{2}}\right)^2}.$

• We implement condlike_rep on our toy data sets with conf_interval now set to TRUE to show the form in which the output now takes. A similar data frame to that above is returned with 95% confidence intervals also included for each adjusted association estimate for each SNP.

out_CL_conf <- condlike_rep(summary_disc=disc_stats, summary_rep=rep_stats, alpha=5e-8, conf_interval=TRUE, conf_level=0.95)
head(out_CL_conf)

[$\star$]{style="color: blue;"} Note: As the current form of condlike_rep uses the R function uniroot which aims to find values for beta_MLE_lower and beta_MLE_upper numerically, it is possible that uniroot may fail to successfully achieve this in some situations. We thus urge users to take care when using condlike_rep to obtain confidence intervals and to be mindful of this potential failure of uniroot.

Method 2: UMVCUE

• The implementation of UMVCUE is very similar to the function described above in the sense that UMVCUE requires the same inputs; discovery and replication data sets in the form of three-columned data frames together with a threshold value, alpha. Furthermore, the outputted data frame is in the same form with just one extra column providing the adjusted estimate, beta_UMVCUE.

• Selection also occurs here at just one stage as SNPs are deemed as significant if their $p$-values corresponding to $\mid \frac{\hat\beta_1}{\sigma_1}\mid$ are smaller than the given threshold.

• The function UMVCUE executes the method detailed in Bowden and Dudbridge (2009). No adaptations have been made to the method described.

• It is worth noting that, as with all conditional likelihood methods, the method used in condlike_rep makes adjustments to each SNP one at a time with no information relating to other SNPs required for this adjustment. However, after ordering SNPs based on significance, for a single SNP, UMVCUE also uses the data of SNPs on either side of it to assist with the adjustment.

• UMVCUE can be applied to the toy data sets as followed, with alpha again specified as 5e-8:

out_UMVCUE <- UMVCUE(summary_disc = disc_stats, summary_rep = rep_stats, alpha = 5e-8)
head(out_UMVCUE)

Method 3: MSE minimization

• The function MSE_minimizer implements a combination method which closely follows that described in Ferguson et al. (2017). The function parameters used here; summary_disc, summary_rep and alpha, are precisely of the same form as those previously detailed in this vignette. In addition, MSE_minimizer has a logical parameter, namely spline which defaults as spline=TRUE. As a smoothing spline is used in the execution of this function, data corresponding to at least 5 SNPs is required.

• An adjusted estimate is computed for each SNP which has been classified as significant in the discovery data set, based on the given threshold. Thus, similar to the above method, MSE_minimizer returns a data frame containing these significant SNPs with 6 columns in which the final column contains the new estimate, beta_joint.

• Following the approach detailed in Ferguson et al. (2017), we define the adjusted linear combination estimator as: $$\hat\beta_{\text{joint}} = \omega(\hat{B}) \cdot \hat\beta_{\text{rep}} + (1-\omega(\hat{B}))\cdot \hat\beta_{\text{disc}}$$ in which $$ \omega(\hat{B}) = \frac{\frac{1}{\sigma^2_{\text{rep}}}}{\frac{1}{\sigma^2_{\text{rep}}}+\frac{1}{\sigma^2_{\text{disc}}+ \hat{B}^2}}.$$ When spline=FALSE is used, we simply let $\hat{B} = \hat\beta_{\text{disc}} - \hat\beta_{\text{rep}}$. We make the assumptions that $\beta_{\text{rep}}$ is unbiased for $\beta$, but $\beta_{\text{disc}}$ is quite likely to be biased and that $\beta_{\text{rep}}$ and $\beta_{\text{disc}}$ are independent.

• For the default setting spline=TRUE, a cubic smoothing spline is applied in which the values of $z_{\text{disc}} = \frac{\hat\beta_{\text{disc}}}{\sigma_{\text{disc}}}$ are considered as inputs and $\hat{B} = \hat\beta_{\text{disc}} - \hat\beta_{\text{rep}}$, the corresponding outputs. The predicted values for $\hat{B}$ from this process, $\hat{B}^*$ say, are then used instead of $\hat{B}$ when computing $\hat\beta_{\text{joint}}$ for each SNP.

• We apply MSE_minimizer to our toy data sets, once with the default setting for spline and once with spline=FALSE. Again for convenient demonstration purposes, we specify the significance threshold as 5e-8.

out_minimizerA <- MSE_minimizer(summary_disc = disc_stats, summary_rep = rep_stats, alpha=5e-8, spline=FALSE)
out_minimizerB <- MSE_minimizer(summary_disc = disc_stats, summary_rep = rep_stats, alpha=5e-8)

head(out_minimizerA)
head(out_minimizerB)

Comparing Results

Just as in the first vignette, we can briefly compare the performance of our correct methods using measures such as the estimated root mean square error of significant SNPs (rmse) and the estimated average bias over all significant SNPs (bias). The significant SNPs we refer to here are those that have been deemed significant at a threshold of $\alpha=5 \times 10^{-8}$ in the discovery GWAS.

## Simulated true effect sizes:
true_beta <- sim_dataset$true$true_beta

The estimated root mean square error of significant SNPs for each method is computed below. It is clear that all methods show an improvement on the estimates obtained from the discovery data set. However, certain further investigation will be required in order to evaluate if the adjusted estimates are less biased or more accurate than the mere use of replication estimates.

## rmse
rmse <- data.frame(disc = sqrt(mean((out_CL$beta_disc - true_beta[out_CL$rsid])^2)), rep = sqrt(mean((out_CL$beta_rep - true_beta[out_CL$rsid])^2)), CL_com = sqrt(mean((out_CL$beta_com - true_beta[out_CL$rsid])^2)), CL_MLE = sqrt(mean((out_CL$beta_MLE - true_beta[out_CL$rsid])^2)), CL_MSE = sqrt(mean((out_CL$beta_MSE - true_beta[out_CL$rsid])^2)), UMVCUE = sqrt(mean((out_UMVCUE$beta_UMVCUE - true_beta[out_UMVCUE$rsid])^2)), minimizerA = sqrt(mean((out_minimizerA$beta_joint - true_beta[out_minimizerA$rsid])^2)), minimizerB = sqrt(mean((out_minimizerB$beta_joint - true_beta[out_minimizerB$rsid])^2)))
rmse

The next metric, the average bias over all significant SNPs with positive association estimates, is included below.

## bias positive
pos_sig <- out_CL$rsid[out_CL$beta_disc > 0]
pos_sigA <- which(out_CL$rsid %in% pos_sig)

bias_up <- data.frame(disc = mean(out_CL$beta_disc[pos_sigA] - true_beta[pos_sig]), rep = mean(out_CL$beta_rep[pos_sigA] - true_beta[pos_sig]), CL_com = mean(out_CL$beta_com[pos_sigA] - true_beta[pos_sig]), CL_MLE = mean(out_CL$beta_MLE[pos_sigA] - true_beta[pos_sig]), CL_MSE = mean(out_CL$beta_MSE[pos_sigA] - true_beta[pos_sig]), UMVCUE = mean(out_UMVCUE$beta_UMVCUE[pos_sigA] - true_beta[pos_sig]), minimizerA = mean(out_minimizerA$beta_joint[pos_sigA] - true_beta[pos_sig]), minimizerB = mean(out_minimizerB$beta_joint[pos_sigA] - true_beta[pos_sig]))
bias_up

In a similar manner, the average bias over all significant SNPs with negative association estimates, is computed.

## bias negative
neg_sig <- out_CL$rsid[out_CL$beta_disc < 0]
neg_sigA <- which(out_CL$rsid %in% neg_sig)

bias_down <- data.frame(disc = mean(out_CL$beta_disc[neg_sigA] - true_beta[neg_sig]), rep = mean(out_CL$beta_rep[neg_sigA] - true_beta[neg_sig]), CL_com = mean(out_CL$beta_com[neg_sigA] - true_beta[neg_sig]), CL_MLE = mean(out_CL$beta_MLE[neg_sigA] - true_beta[neg_sig]), CL_MSE = mean(out_CL$beta_MSE[neg_sigA] - true_beta[neg_sig]), UMVCUE = mean(out_UMVCUE$beta_UMVCUE[neg_sigA] - true_beta[neg_sig]), minimizerA = mean(out_minimizerA$beta_joint[neg_sigA] - true_beta[neg_sig]), minimizerB = mean(out_minimizerB$beta_joint[neg_sigA] - true_beta[neg_sig]))
bias_down

To complement the above, we provide an illustration of boxplots obtained for the root mean square error of significant SNPs (RMSE of sig. SNPs at $5 \times 10^{-8}$), plotted for each Winner's Curse correction method (Method).

library(RColorBrewer)
library(ggplot2)
col <- brewer.pal(8,"Dark2")
col1 <- brewer.pal(11,"RdYlBu")

all_results <- data.frame(rsid = c(rep(out_CL$rsid,8)), beta_disc = c(rep(out_CL$beta_disc,8)), se_disc = c(rep(out_CL$se_disc,8)), adj_beta = c(out_CL$beta_disc,out_CL$beta_rep,out_CL$beta_com,out_CL$beta_MLE,out_CL$beta_MSE,out_UMVCUE$beta_UMVCUE,out_minimizerA$beta_joint,out_minimizerB$beta_joint), method = c(rep("disc",33),rep("rep",33),rep("CL_com",33),rep("CL_MLE",33),rep("CL_MSE",33),rep("UMVCUE",33),rep("minimizerA",33),rep("minimizerB",33)))
all_results$rmse <- sqrt((all_results$adj_beta - true_beta[all_results$rsid])^2)
all_results$method <- factor(all_results$method, levels=c("disc","rep","CL_com", "CL_MLE", "CL_MSE", "UMVCUE", "minimizerA", "minimizerB"))

ggplot(all_results,aes(x=method,y=rmse,fill=method, color=method)) + geom_boxplot(size=0.7,aes(fill=method, color=method, alpha=0.2)) + scale_fill_manual(values=c(col[1],col[2],col[3],col[4],col[5],col[6],col[7],col[8])) + scale_color_manual(values=c(col[1],col[2],col[3],col[4],col[5],col[6],col[7],col[8]))  + xlab("Method") +
  ylab(expression(paste("RMSE of sig. SNPs at  ", 5%*%10^-8))) + theme_bw() + geom_hline(yintercept=0, colour="black") +  theme(axis.text.x=element_text(angle=90, vjust=0.5, hjust=1),text = element_text(size=12),legend.position = "none", strip.text = element_text(face="italic")) 

In addition, we can gain a visual insight into the adjustments made by these functions by constructing a density plot with the adjusted absolute values along with the naive estimates and the true absolute $\beta$ values of significant SNPs, as follows:

true <- data.frame(rsid = c(out_CL$rsid), beta_disc =c(out_CL$beta_disc), se_disc =c(out_CL$se_disc),adj_beta=true_beta[out_CL$rsid],method=c(rep("true",33)))
all_resultsA <- rbind(all_results[,1:5],true)

ggplot(all_resultsA, aes(x=abs(adj_beta),colour=method,fill=method)) + geom_density(alpha=0.05,size=1) + scale_fill_manual(values=c(col[1],col[2],col[3],col[4],col[5],col[6],col[7],col[8],col1[11])) + scale_color_manual(values=c(col[1],col[2],col[3],col[4],col[5],col[6],col[7],col[8],col1[11])) + xlim(-0.01,0.08) +
  ylab("Density") + xlab(expression(paste("|", beta, "| " , "of sig. SNPs at  ", 5%*%10^-8))) + theme_bw() +  theme(text = element_text(size=12)) + labs(fill = "Method",colour="Method")

[$\star$]{style="color: blue;"} Note: In the above plot, it can be seen that there must be very little difference between the replication estimates and the adjusted estimates obtained using the UMVCUE method as the density curves of rep and UMVCUE can be seen to nearly overlap completely.

$~$ $~$

Using empirical Bayes and bootstrap methods with replication data sets

When a replication data set is also available, as has been described throughout this vignette, we also potentially have the option to employ the empirical Bayes and bootstrap methods. We have seen this work well in simulations, especially in terms of reducing the mean square error (MSE) and thus, consider exploration of their implementation in this setting. With data in the form described above similar to disc_stats and rep_stats, implementation of both methods could take place on the combined estimator as shown below:

## combined estimator:
com_stats <- data.frame(rsid = disc_stats$rsid, beta = ((((rep_stats$se)^2)*(disc_stats$beta))+(((disc_stats$se)^2)*(rep_stats$beta)))/(((disc_stats$se)^2) + ((rep_stats$se)^2)), se = sqrt((((disc_stats$se)^2)*((rep_stats$se)^2))/(((disc_stats$se)^2) + ((rep_stats$se)^2))))

## apply methods:
out_EB_com <- empirical_bayes(com_stats)
out_boot_com <- BR_ss(com_stats,seed_opt=TRUE,seed=2020)

## rearrange data frames with SNPs ordered 1,2,3.. 
out_EB_com <- dplyr::arrange(out_EB_com,out_EB_com$rsid)
out_boot_com <- dplyr::arrange(out_boot_com,out_boot_com$rsid)
out_EB_com <- data.frame(rsid = disc_stats$rsid, beta_disc = disc_stats$beta, se_disc  = disc_stats$se, beta_rep =rep_stats$beta, se_rep = rep_stats$se, beta_EB=out_EB_com$beta_EB)
out_boot_com <- data.frame(rsid = disc_stats$rsid, beta_disc = disc_stats$beta, se_disc  = disc_stats$se, beta_rep =rep_stats$beta, se_rep = rep_stats$se, beta_boot=out_boot_com$beta_BR_ss)

## reorder data frames based on significance in discovery data set:
out_EB_com <- dplyr::arrange(out_EB_com, dplyr::desc(abs(out_EB_com$beta_disc/out_EB_com$se_disc)))
out_EB_com <- out_EB_com[abs(out_EB_com$beta_disc/out_EB_com$se_disc) > stats::qnorm((5e-8)/2, lower.tail=FALSE),]
head(out_EB_com)

out_boot_com <- dplyr::arrange(out_boot_com, dplyr::desc(abs(out_boot_com$beta_disc/out_boot_com$se_disc)))
out_boot_com <- out_boot_com[abs(out_boot_com$beta_disc/out_boot_com$se_disc) > stats::qnorm((5e-8)/2, lower.tail=FALSE),]
head(out_boot_com)

We now compute similar evaluation metrics to above and produce the two plots in order to demonstrate the performance of the above approaches.

## rmse
rmse <- data.frame(disc = sqrt(mean((out_CL$beta_disc - true_beta[out_CL$rsid])^2)), rep = sqrt(mean((out_CL$beta_rep - true_beta[out_CL$rsid])^2)), EB_com = sqrt(mean((out_EB_com$beta_EB - true_beta[out_CL$rsid])^2)), boot_com = sqrt(mean((out_boot_com$beta_boot - true_beta[out_CL$rsid])^2)))
rmse

## bias positive
bias_up <- data.frame(disc = mean(out_CL$beta_disc[pos_sigA] - true_beta[pos_sig]), rep = mean(out_CL$beta_rep[pos_sigA] - true_beta[pos_sig]), EB_com = mean(out_EB_com$beta_EB[pos_sigA] - true_beta[pos_sig]), boot_com = mean(out_boot_com$beta_boot[pos_sigA] - true_beta[pos_sig]))
bias_up

## bias negative
bias_down <- data.frame(disc = mean(out_CL$beta_disc[neg_sigA] - true_beta[neg_sig]), rep = mean(out_CL$beta_rep[neg_sigA] - true_beta[neg_sig]), EB_com = mean(out_EB_com$beta_EB[neg_sigA] - true_beta[neg_sig]), boot_com = mean(out_boot_com$beta_boot[neg_sigA] - true_beta[neg_sig]))
bias_down

par(mfrow = c(2, 1))
all_results <- data.frame(rsid = c(rep(out_CL$rsid,4)), beta_disc = c(rep(out_CL$beta_disc,4)), se_disc = c(rep(out_CL$se_disc,4)), adj_beta = c(out_CL$beta_disc,out_CL$beta_rep,out_EB_com$beta_EB,out_boot_com$beta_boot), method = c(rep("disc",33),rep("rep",33),rep("EB_com",33),rep("boot_com",33)))
all_results$rmse <- sqrt((all_results$adj_beta - true_beta[all_results$rsid])^2)
all_results$method <- factor(all_results$method, levels=c("disc","rep","EB_com", "boot_com"))
ggplot(all_results,aes(x=method,y=rmse,fill=method, color=method)) + geom_boxplot(size=0.7,aes(fill=method, color=method, alpha=0.2)) + scale_fill_manual(values=c(col[1],col[2],col[3],col[4])) + scale_color_manual(values=c(col[1],col[2],col[3],col[4]))  + xlab("Method") +
  ylab(expression(paste("RMSE of sig. SNPs at  ", 5%*%10^-8))) + theme_bw() + geom_hline(yintercept=0, colour="black") +  theme(axis.text.x=element_text(angle=90, vjust=0.5, hjust=1),text = element_text(size=10),legend.position = "none", strip.text = element_text(face="italic")) 
true <- data.frame(rsid = c(out_CL$rsid), beta_disc =c(out_CL$beta_disc), se_disc =c(out_CL$se_disc),adj_beta=true_beta[out_CL$rsid],method=c(rep("true",33)))
all_resultsA <- rbind(all_results[,1:5],true)
ggplot(all_resultsA, aes(x=abs(adj_beta),colour=method,fill=method)) + geom_density(alpha=0.05,size=1) + scale_fill_manual(values=c(col[1],col[2],col[3],col[4],col[8])) + scale_color_manual(values=c(col[1],col[2],col[3],col[4],col[8])) + xlim(-0.01,0.08) +
  ylab("Density") + xlab(expression(paste("|", beta, "| " , "of sig. SNPs at  ", 5%*%10^-8))) + theme_bw() +  theme(text = element_text(size=10),legend.position="bottom") + labs(fill = "Method",colour="Method") +guides(fill=guide_legend(nrow=2,byrow=TRUE))

amandaforde/winnerscurse documentation built on March 9, 2024, 6:09 p.m.