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Use the example from Data preparation. We provide
organize data
and organize_ld
function to do
the sanity check and organize the summary statistics and LD into the
MESuSiE input format
library(dplyr)
library(MESuSiE)
load("/net/fantasia/home/borang/Susie_Mult/meSuSie_Analysis/data/MESuSiE_Example.RData")
summ_stat_list<-organize_gwas(UKBB_example%>%rename(SNP = CHR_POS),GLGC_example%>%rename(SNP = CHR_POS),c("EUR","AFR"))
colnames(WB_cov)<-UKBB_example$CHR_POS
colnames(BB_cov)<-GLGC_example$CHR_POS
LD_list<-organize_ld(WB_cov,BB_cov,summ_stat_list)
MESuSiE_res<-meSuSie_core(LD_list,summ_stat_list,L=10)
*************************************************************
Multiple Ancestry Sum of Single Effect Model (MESuSiE)
Visit http://www.xzlab.org/software.html For Update
(C) 2022 Boran Gao, Xiang Zhou
GNU General Public License
*************************************************************
# Start data processing for sufficient statistics
# Create MESuSiE object
# Start data analysis
# Data analysis is done, and now generates result
Potential causal SNPs with PIP > 0.5: 22_21958872
Credible sets for effects:
$cs
$cs$L1
[1] 7 8 26 38 40 41 57 61 62 69 71 79 82
$cs_category
L1
"EUR_AFR"
$purity
min.abs.corr mean.abs.corr median.abs.corr
L1 0.9978499 0.9991224 0.9992341
$cs_index
[1] 1
$coverage
[1] 0.9551583
$requested_coverage
[1] 0.95
Use MESuSiE_Plot() for visualization
# Total time used for the analysis: 0.07 mins
The MESuSiE results can be interpreted in terms of the 95% credible set and SNP-level Posterior Inclusion Probabilities (PIPs).
For instance, in the provided example, the credible set contains 13
SNPs labeled as EUR_AFR
, indicating these SNPs are shared
across multiple ancestries.
PIPs We used a PIP cutoff of 0.5 to declare signal.
MESuSiE_res$pip[MESuSiE_res$cs$cs$L1]
[1] 0.02617149 0.02411160 0.04600253 0.03558618 0.02805318 0.03538103
[7] 0.02041509 0.05667729 0.05446116 0.04994392 0.52385726 0.02241395
[13] 0.03208367
In the example provided, one SNP exhibits a PIP greater than 0.5. However, this does not inform us whether the SNP is shared or ancestry-specific. To make that inference, we need to further analyze the PIP values for shared or ancestry-specific effects, which is the unique feature provided by MESuSiE.
MESuSiE_res$pip_config[MESuSiE_res$cs$cs$L1,]
EUR AFR EUR_AFR
[1,] 0.0003748811 0.0002535134 0.02617115
[2,] 0.0003748810 0.0002532205 0.02411128
[3,] 0.0003748798 0.0002476710 0.04600234
[4,] 0.0003748806 0.0002482805 0.03558589
[5,] 0.0003748802 0.0002483030 0.02805295
[6,] 0.0003748805 0.0002483253 0.03538074
[7,] 0.0003748796 0.0002484404 0.02041492
[8,] 0.0003748794 0.0002484522 0.05667714
[9,] 0.0003748793 0.0002485671 0.05446102
[10,] 0.0003748793 0.0002480695 0.04994379
[11,] 0.0003748793 0.0002610915 0.52385712
[12,] 0.0003748795 0.0002468203 0.02241380
[13,] 0.0003748793 0.0002458986 0.03208353
From the results, SNP with a PIP greater than 0.5 represents a shared causal signal.
When running meSuSie_core
, various tuning parameters can
be adjusted to refine the results:
L
): Specify the
number of effects to consider.prior_weights
): This
represents the prior probability of a SNP being causal. By default, it
is set to . Users can adjust this parameter to incorporate functional
annotation into MESuSiE.ancestry_weight
):
Configure the weighting for different ancestries. We set the ratio of
ancestry-specific to shared as 3:1 to encourage the ancestry-specific
causal SNP detection.
estimate_residual_variance
): This parameter can
be set to either TRUE or FALSE. When set to TRUE, the residual variance
is estimated, while when set to FALSE, it is fixed at one. For
multi-ancestry GWAS fine-mapping, it’s typically advisable to fix the
residual variance at one to enhance robustness, given that the
heritability of the local region is often minimal. However, when using
MESuSiE for multi-ancestry eQTL fine-mapping, it’s recommended to
estimate the residual variance since the heritability of the gene
expression is relatively significant.cor_method & cor_threshold
):
min_abs_corr
, representing the minimum absolute correlation
permissible within a credible set across ancestries. This is a prevalent
threshold for genotype data in genetic studies.min_abs_corr
. By default, this is set to 0.5.Note: We’ve made available function
meSuSie_get_cs
allowing users to tweak the results based on varyingcor_method
andcor_threshold
. The best part? You can adjust without having to rerun the entire analysis.
MESuSiE_Plot(MESuSiE_res,LD_list,summ_stat_list)
sessionInfo()
R version 4.3.1 (2023-06-16)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Ubuntu 20.04.6 LTS
Matrix products: default
BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/liblapack.so.3; LAPACK version 3.9.0
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
time zone: America/New_York
tzcode source: system (glibc)
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] MESuSiE_1.0 dplyr_1.1.2 workflowr_1.7.0
loaded via a namespace (and not attached):
[1] gtable_0.3.1 xfun_0.39 bslib_0.5.0
[4] ggplot2_3.4.2 processx_3.8.0 ggrepel_0.9.1
[7] lattice_0.20-45 callr_3.7.3 vctrs_0.6.2
[10] tools_4.3.1 ps_1.7.2 generics_0.1.3
[13] tibble_3.2.1 fansi_1.0.5 highr_0.10
[16] pkgconfig_2.0.3 Matrix_1.5-4.1 data.table_1.14.8
[19] lifecycle_1.0.3 compiler_4.3.1 farver_2.1.1
[22] stringr_1.5.0 git2r_0.32.0 progress_1.2.2
[25] munsell_0.5.0 getPass_0.2-2 httpuv_1.6.11
[28] htmltools_0.5.5 sass_0.4.6 yaml_2.3.7
[31] later_1.3.1 pillar_1.9.0 nloptr_2.0.3
[34] crayon_1.5.2 jquerylib_0.1.4 whisker_0.4.1
[37] tidyr_1.3.0 ellipsis_0.3.2 cachem_1.0.8
[40] tidyselect_1.2.0 digest_0.6.30 stringi_1.7.12
[43] purrr_1.0.1 labeling_0.4.2 RcppArmadillo_0.11.1.1.0
[46] cowplot_1.1.1 rprojroot_2.0.3 fastmap_1.1.1
[49] grid_4.3.1 colorspace_2.1-0 cli_3.6.1
[52] magrittr_2.0.3 utf8_1.2.3 withr_2.5.1
[55] prettyunits_1.2.0 scales_1.2.1 promises_1.2.0.1
[58] rmarkdown_2.22 httr_1.4.6 hms_1.1.2
[61] evaluate_0.18 knitr_1.39 irlba_2.3.5.1
[64] rlang_1.1.1 Rcpp_1.0.11 mixsqp_0.3-48
[67] glue_1.6.2 rstudioapi_0.14 jsonlite_1.8.3
[70] R6_2.5.1 fs_1.6.2