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Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.

Ole A Andreassen, Wesley K Thompson, Andrew J Schork, Stephan Ripke, Morten Mattingsdal, John R Kelsoe, Kenneth S Kendler, Michael C O'Donovan, Dan Rujescu, Thomas Werge, Pamela Sklar, J Cooper Roddey, Chi-Hua Chen, Linda McEvoy, Rahul S Desikan, Srdjan Djurovic, Anders M Dale.   

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Year:  2015        PMID: 26540268      PMCID: PMC4634985          DOI: 10.1371/journal.pgen.1005544

Source DB:  PubMed          Journal:  PLoS Genet        ISSN: 1553-7390            Impact factor:   6.020


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Incorrect mathematical definition of the conjunction FDR in the section ‘Conjunction statistics—test of association with both phenotypes’ Under the sub-heading of ‘Conjunction statistics—test of association with both phenotypes’ in the ‘Materials and Methods’ section of the manuscript, there are errors in the mathematical definition of the conjunction FDR. The authors have provided an updated version here with corrections to the text in bold: In order to identify which of the SNPs were associated with schizophrenia and bipolar disorder we used a conjunction FDR procedure similar to that described for p-value statistics in Nichols et al. [45]. This minimizes the effect of a single phenotype driving the common association signal. Conjunction FDR is defined as the posterior probability that a given SNP is null for either phenotype or both phenotypes simultaneously when the p-values for both phenotypes are as small or smaller than the observed p-values. Formally, conjunction FDR is given by where π Conditional empirical cdfs provide a model-free method to obtain conservative estimates of Eq (6). This can be seen as follows. Estimate the conjunction FDR by where FDRSCZ|BD and FDRBD| SCZ (the estimated conditional FDRs described above) are conservative (upwardly biased) estimates of Eq. [5]. Thus, Eq (7) is a conservative estimate of max{p1/F(p1| p2), p2/F(p2|p1)} = max{p F (p )/F(p , p ), p F (p )/F(p , p )}, with F (p ) and F (p ) the marginal non-null cdfs of SNPs for SCZ and BD, respectively. For enriched samples, p-values will tend to be smaller than predicted from the uniform distribution, so that F1(p1) ≥ p1 and F2(p2) ≥ p2. Then Under the assumption that SNPs are independent if one or both are null, reasonable for disjoint samples, this last quantity is precisely the conjunction FDR given in Eq (. Thus, Eq (7) is a conservative model-free estimate of the conjunction FDR. We present a complementary model-based approach to estimating conjunction FDR in the S1 Text. We assigned the conjunction FDR values by interpolation into a bi-directional two-dimensional look-up table (S3 Fig). All SNPs with conjunction FDR<0.05 (−log10(FDR)>1.3) with schizophrenia and bipolar disorder considered jointly are listed in Table 3 (after pruning), together with the corresponding z-scores and minor alleles. The z-scores were calculated from the p-values and the direction of effect was determined by the risk allele.
Table 3

Conjunction FDR; pleiotropic loci in SCZ and BD (SCZ&BD).

locusSNPneighbor geneChrA1A2conjfdr BD&SCZz-score BDz-score SCZ
1rs2252865 RERE 1p36.23 TC0.0303.6963.494
2rs4650608 IFI44 1p31.1 TC0.0433.2893.711
4rs11205362 PRP3 1q21.1 GA0.0333.4043.262
8rs9834970 TRANK1 3p22.2 CT0.0273.4703.965
9rs4687657 ITIH4† 3p21.1 GT0.0283.7873.781
11rs3134942 NOTCH4† 6p21.3 GT0.0483.2513.571
15rs3757440 MAD1L1 7p22 AG0.0313.4903.425
20rs10883757 TRIM8 10q24.3 CT0.0403.2613.046
22rs1006737 CACNA1C† 12p13.3 AG0.0224.5534.137
26rs961196 TTC7B 14q32.11 CT0.0443.6182.960
28rs12708772 SHISA9 16p13.12 CT0.0443.2942.955
31rs1800359 ZNF276 16q24.3 AG0.0353.3293.165
33rs159788 BC039673 20p13 GA0.0343.411-3.232
35rs381523 PPM1F 22q11.22 AG0.0453.2203.166

Independent complex or single gene loci (r2 < 0.2) with SNP(s) with a conjunctional FDR (conjFDR) < 0.05 in schizophrenia (SCZ) and bipolar disorder (BD). All SNPs with a conjFDR value < 0.05 (bidirectional association, i.e. association with SCZ given association with BD (condFDR< 0.05) and association with BD given association with SCZ (condFDR<0.05)) are listed and sorted in each LD block. We defined the most significant SNP in each LD block based on the minimum conjFDR. All independent loci are listed consecutively, and the same locus number are used as in the condFDR < 0.05 results (Table 1). Chromosome (Chr). Z-scores for each pleiotropic locus are provided, with minor allele (A1) and major allele (A2). All data were first corrected for genomic inflation. †Same locus identified in previous BD or SCZ genome-wide association studies.

Independent complex or single gene loci (r2 < 0.2) with SNP(s) with a conjunctional FDR (conjFDR) < 0.05 in schizophrenia (SCZ) and bipolar disorder (BD). All SNPs with a conjFDR value < 0.05 (bidirectional association, i.e. association with SCZ given association with BD (condFDR< 0.05) and association with BD given association with SCZ (condFDR<0.05)) are listed and sorted in each LD block. We defined the most significant SNP in each LD block based on the minimum conjFDR. All independent loci are listed consecutively, and the same locus number are used as in the condFDR < 0.05 results (Table 1). Chromosome (Chr). Z-scores for each pleiotropic locus are provided, with minor allele (A1) and major allele (A2). All data were first corrected for genomic inflation. †Same locus identified in previous BD or SCZ genome-wide association studies. Incorrect mathematical definition of the conjunction FDR in the ‘Conditional and Conjunction Local False Discovery Rate’ section of the . There are also errors under the sub-heading ‘Conditional and Conjunction Local False Discovery Rate’ in the S1 Text. Please view the correct S1 Text here, with updates to the text in red.

Conjunction FDR bi-directional 2-D Look-up table.

(DOC) Click here for additional data file.

Supporting statistical methods.

(DOC) Click here for additional data file.
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