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The window posterior probabilities of association (WPPA) of candidate windows (i.e. with at least 0.2% genetic variance) was at least 1.5-fold greater than the average WPPA of 1 Mb windows across the genome.
On the contrary, TEE has a much better window to the posterior structures of thorax.
The genome was divided into non-overlapping 1 Mb windows and the posterior distribution of the percentage of genetic variance attributed to each window was constructed from the MCMC samples (e.g. [ 39]).
Accordingly, we only kept windows predicted with posterior probability > 0.95, resulting in 42,297 and 55,624 active intragenic enhancer windows in K562 and GM12878, respectively.
Just like in Experiment 1, differences of scalp distributions for the P1, N1 and 200 260 time-windows within the posterior region were tested.
Furthermore, we identified 57 1-Mb withows with a posterior probability of inclusion (> 0.90) that harbor genetic variation associated with individual fatty acid content.
All of the averaging results in this paper were obtained with an Occam's window defined using a minimal posterior odds ratio of OCC = 1/20.
Open image in new window Fig. 8 Posterior attachment of lateral meniscus.
Open image in new window Fig. 14 Posterior vitreous detachment (PVD) in two patients.
Open image in new window Fig. 7 Posterior lateral meniscus tear.
Open image in new window Fig. 16 Posterior densities of the regression coefficients.
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