Difference between revisions of "RAREMETAL METHOD"

Revision as of 19:23, 27 March 2014

The key idea behind meta-analysis with RAREMETAL is that various gene-level test statistics can be reconstructed from single variant score statistics and that, when the linkage disequilibrium relationships between variants are known, the distribution of these gene-level statistics can be derived and used to evaluate signifi-cance. Single variant statistics are calculated using the Cochran-Mantel-Haenszel method. The main formulae are tabulated in the following:

**Formulae for RAREMETAL**
Test	Statistics	Null Distribution	Notation
Single Variant	$T=\sum_{i=1}^n {U_i}\bigg/\sqrt{\sum_{i=1}^n{V_i}}$	$T\sim\mathbf{N}(0,1)$	$U_i \text{ is the score statistic from study }i;$ $V_i \text{ is the variance of } U_i.$
un-weighted Burden	$T_b=\sum_{i=1}^n{\mathbf{U_i}}\Big/\sqrt{\sum_{i=1}^n{\mathbf{V_i}}}$	$T_b\sim\mathbf{N}(0,1)$	$\mathbf{U_i}\text{ is the vector of score statistics from study }i, or$ $\mathbf{U_i}=\{U_{i1},...,U_{im}\};$ $\mathbf{V_i} \text{ is the covariance of } \mathbf{U_i}.$
Weighted Burden	$T_{wb}=\mathbf{w^T}\sum_{i=1}^n{\mathbf{U_i}}\bigg/\sqrt{\mathbf{w^T}\left(\sum_{i=1}^n{\mathbf{V_i}}\right)\mathbf{w}}$	$T_{wb}\sim\mathbf{N}(0,1)$	$\mathbf{w^T}=\{w_1,w_2,...,w_m\}^T \text{ is the weight vector.}$
VT	$T_{VT}=\max(T_{b\left(f_1\right)},T_{b\left(f_2\right)},\dots,T_{b\left(f_m\right)}),\text{ where}$ $T_{b\left(f_j\right)}=\boldsymbol{\phi}_{f_j}^\mathbf{T}\sum_{i=1}^n{\mathbf{U_i}}\bigg/\sqrt{\boldsymbol{\phi}_{f_j}^\mathbf{T}\left(\sum_{i=1}^n{\mathbf{V_i}}\right)\boldsymbol{\phi}_{f_j}}$	$\left(T_{b\left(f_1\right)},T_{b\left(f_2\right)},\dots,T_{b\left(f_m\right)}\right)$ $\sim\mathbf{MVN}\left(\mathbf{0},\boldsymbol{\Omega}\right)\text{,}$ $\text{where }\boldsymbol{\Omega_{ij}}=\frac{\boldsymbol{\phi}_{f_i}^T\left(\sum_{i=1}^n{\mathbf{V_i}}\right)\boldsymbol{\phi}_{f_j}}{\sqrt{\boldsymbol{\phi}_{f_i}^T\left(\sum_{i=1}^n{\mathbf{V_i}}\right)\boldsymbol{\phi}_{f_i}}\sqrt{\boldsymbol{\phi}_{f_j}^T\left(\sum_{i=1}^n{\mathbf{V_i}}\right)\boldsymbol{\phi}_{f_j}}}$	$\boldsymbol{\phi}_{f_j}\text{ is a vector of } 0 \text{s and } 1\text{s,}$ $\text{indicating the inclusion of a variant using threshold }f_j;$
SKAT	$\mathbf{Q}=\left(\sum_{i=1}^n{\mathbf{U_i^T}}\right) \mathbf{W}\left(\sum_{i=1}^n{\mathbf{U_i}}\right)$	$\mathbf{Q}\sim\sum_{i=1}^m{\lambda_i\chi_{1,i}^2},\text{ where}$ $\left(\lambda_1,\lambda_2,\dots,\lambda_m\right)\text{ are eigen values of}$ $\left(\sum_{i=1}^n{\mathbf{V_i}}\right)^\frac{1}{2}\mathbf{W}\left(\sum_{i=1}^n{\mathbf{V_i}}\right)^\frac{1}{2}$	$\mathbf{W}\text{ is a diagonal matrix of weights.}$

@@ Line 1: / Line 1: @@
-==Single Variant Meta Analysis ==
-== Gene-level Meta Analysis ==
-=== Burden Test ===
-=== Madson-Browning Burden Test ===
-=== Variable Threshold Test ===
-=== SKAT ===
-== Conditional Analysis ==
 The key idea behind meta-analysis with RAREMETAL is that various gene-level test statistics can be reconstructed from single variant score statistics and that, when the linkage disequilibrium relationships between variants are known, the distribution of these gene-level statistics can be derived and used to evaluate signifi-cance. Single variant statistics are calculated using the Cochran-Mantel-Haenszel method. The main formulae are tabulated in the following:

Difference between revisions of "RAREMETAL METHOD"

Revision as of 19:23, 27 March 2014

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