Case study: JAZF1 xQTL and AD GWAS¶

This notebook documents the analysis of xQTL case study on a targeted gene, JAZF1.

  • Section 0: Sanity check
  • Section 1: Fine-mapping for xQTL and GWAS
  • Section 2: Multi-context colocalization with Bellenguez 2022
  • Section 3: Refinement of colocalized loci with other AD GWAS
  • Section 4: Assessment of multi-context xQTL effect sizes
  • Section 5: Multi-context causal TWAS (including conventional TWAS and MR)
  • Section 6: Context specific multi-gene fine-mapping
  • Section 7: Epigenomic QTL and their target regions
  • Section 8: Context focused validation in other xQTL data
  • Section 9: Non-linear effects of xQTL
  • Section 10: in silico functional studies in iPSC model
  • Section 11: Functional annotations of selected loci
  • Section 12: Candidate loci as trans-xQTL

Overview¶

FunGen-xQTL resource contains 67 xQTL contexts as well as 9 AD GWAS fine-mapped genome-wide. The overarching goal for case studies is to use these resource to raise questions and learn more about gene targets of interest.

Overall, a case study consists of the following aspects:

  • Check the basic information of the gene
  • Check the existing xQTL and integrative analysis results, roughly including
    • Summary table for univariate fine-mapping
    • Marginal association results
    • Multi-gene and multi-context fine-mapping
    • Multi-context colocalization with AD GWAS
    • TWAS, MR and causal TWAS
    • Integration with epigenetic QTL
    • Quantile QTL
    • Interaction QTL
    • Validation:
      • Additional xQTL data in FunGen-xQTL
      • Additional AD GWAS data-set already generated by FunGen-xQTL
    • In silico functional studies
      • Additional iPSC data-sets
    • Functional annotations of variants, particularly in relevant cellular contexts
  • Creative thinking: generate hypothesis, search in literature, raise questions to discuss

Computing environment setup¶

Interactive analysis will be done on AWS cloud powered by MemVerge. Please contact Gao Wang to setup accounts for you to start the analysis.

Please follow instructions on https://wanggroup.org/productivity_tips/mmcloud-interactive to configure your computing environment. Here are some additional packages you need to install after the initial configuration, in order to perform these analysis:

micromamba install -n r_libs r-pecotmr
micromamba install -n r_libs r-bedmatrix

How to Use This Notebook¶

  1. Before you start: Load functions from cb_plot.R and utilis.R, located at /data/interactive_analysis/rf2872/codes/. These functions and resources are packaged to streamline the analysis and ensure everything is as clean as possible. And also the codes for ColocBoost under path /data/colocalization/colocboost/R.
  2. Inside of this notebook, use sed -i or Ctrl+F to replace the gene JAZF1 with the gene you want to analyze.
  3. For detailed analysis in some sections, please refer to the corresponding analysis notebooks as indicated. These companion notebooks are available under this same folder. The rest of the tasks can be completed with a few lines of code, as demonstrated in this notebook.
  4. Similarly for the companion notebooks you should also use the sed -i or Ctrl+F replacing gene_name (JAZF1 in this case) with the gene you want to investigate.

While using this notebook, you may need to generate three intermediate files from Sections 1 and 2, which will be useful for downstream analysis:

  • a. Section 1:
    • Fine-mapping contexts that indicate shared signals with AD, JAZF1_finemapping_contexts.rds. This can be used as input for Section 8 the multi-cohort validation step
    • A subset of the xQTL-AD table, Fungen_xQTL_allQTL.overlapped.gwas.export.JAZF1.rds. This can be used as input for Section 12.
  • b. Section 2: A variant list showing colocalization in cohorts we analyzed with ColocBoost, JAZF1_colocboost_res.rds. this can be used as input for Sections 7, 9, 10, and 12.

Section 0: Sanity check¶

Check the basic information of the gene¶

  • To gain a preliminary understanding of this gene’s expression—specifically, whether it is cell-specific—can help us quickly determine if our results are consistent with expectations.

Useful websites:

  1. check gene function, (immune) cell type specificity, tissue specifity, protein location: https://www.proteinatlas.org
  2. check gene position and structure: https://www.ncbi.nlm.nih.gov/gene/
  3. other collective information: https://www.genecards.org

Check the existing results which are inputs to this analysis¶

In [67]:
source('../../codes/cb_plot.R')
source('../../codes/utilis.R')
for(file in list.files("/data/colocalization/colocboost/R", pattern = ".R", full.names = T)){
          source(file)
        }
gene_name = 'JAZF1'

dir.create(paste0('plots/', gene_name), recursive = T)

get basic target gene information

In [68]:
target_gene_info <- get_gene_info(gene_name = gene_name)
target_gene_info
$gene_info
A data.table: 1 x 14
region_id#chrstartendTSSLD_matrix_idLD_sumstats_idLD_sumstats_id_oldTADB_indexTADB_idgene_startgene_endsliding_windowsgene_name
<chr><chr><dbl><dbl><int><chr><chr><chr><chr><chr><int><int><chr><chr>
ENSG00000153814chr7251200002918079528180794chr7:23432442-25641844,chr7:25641844-28408975,chr7:28408975-309671027_23432442-25641844,7_25641844-28408975,7_28408975-309671027_23432442-25641844,7_25641844_28408975,7_28408975_30967102TADB_620,TADB_621,TADB_622chr7_24118656_29243917,chr7_26830573_29825894,chr7_27953358_318920812818079527830573chr7:21118236-26180356,chr7:21419444-29243917,chr7:22480752-29825894,chr7:24118656-31892081,chr7:26830573-33761787,chr7:27953358-36697459JAZF1
$target_LD_ids
A matrix: 1 x 3 of type chr
chr7:23432442-25641844chr7:25641844-28408975chr7:28408975-30967102
$target_sums_ids
A matrix: 1 x 3 of type chr
7_23432442-256418447_25641844-284089757_28408975-30967102
$gene_region
'chr7:25120000-29180795'
$target_TAD_ids
A matrix: 1 x 3 of type chr
chr7_24118656_29243917chr7_26830573_29825894chr7_27953358_31892081
In [69]:
gene_id = target_gene_info$gene_info$region_id
chrom = target_gene_info$gene_info$`#chr`

Take a quick look for the expression of target gene in ROSMAP bulk data, we don't want them to be too low

In [4]:
source('../../codes/utilis.R')
expression_in_rosmap_bulk(target_gene_info)
No description has been provided for this image

Section 1: Fine-mapping for xQTL and GWAS¶

see notebook

In [14]:
region_p
No description has been provided for this image

Bellenguez et al GWAS signals has many overlap with CS from other xQTL sources. This motivates us to look further. The figure above shows the ranges of CS to give us a loci level idea. Below, we show the variants in those CS, color-coding the variants that are shared between them in the same color. In particular, AD GWAS signals are also captured by a few xQTL data, although at this point we don't have formal statistical (colocalization) evidences for these observations yet.

In [16]:
pip_p
No description has been provided for this image

Section 2: Multi-context colocalization with Bellenguez 2022¶

This is done using ColocBoost. The most updated version of ColocBoost results are under path s3://statfungen/ftp_fgc_xqtl/analysis_result/ColocBoost/2024_9/

In [13]:
cb_res <- readRDS(paste0("/data/analysis_result/ColocBoost/2024_9/",gene_id,"_res.rds") )
In [14]:
#save colocboost results
cb_res_table <- get_cb_summary(cb_res) 

saveRDS(cb_res_table, paste0(gene_name, "_colocboost_res.rds"))
In [7]:
cb <- plot_cb(cb_res = cb_res, cex.pheno = 1.5, x.phen = -0.2)
No description has been provided for this image
In [8]:
pdf('plots/JAZF1/sec2.colocboost_res.pdf', width = 10, height = 5)
replayPlot(cb$p)
dev.off()
pdf: 2
In [9]:
# colocalized variants
cb_res_table
A data.frame: 3 x 8
colocalized phenotypespurity# variantshighest VCPcolocalized indexcolocalized variantsmax_abs_z_variantcset_id
<chr><dbl><dbl><dbl><chr><chr><chr><chr>
AC_unproductive; DLPFC_unproductive; PCC_unproductive1.0000000 11.000000012479 chr7:27913416:A:G chr7:27913416:A:Gcoloc_sets:Y12_Y13_Y15:CS1
Mic; OPC; AC; AD_Bellenguez_2022 0.9808940 90.148192213387; 13318; 13315; 13383; 13313; 13389; 13368; 13363; 13365 chr7:28138643:G:T; chr7:28116987:C:G; chr7:28117268:C:T; chr7:28118439:C:T; chr7:28136686:G:A; chr7:28137682:C:T; chr7:28130784:T:C; chr7:28132564:A:G; chr7:28132395:C:T chr7:28116987:C:Gcoloc_sets:Y1_Y4_Y8_Y16:CS2
Ast; Exc 0.6362281200.321209313576; 13545; 13546; 13245; 13433; 13397; 13452; 13458; 13456; 13443; 13459; 13470; 13472; 13413; 13416; 13388; 13667; 13390; 13529; 13350chr7:28102567:G:T; chr7:28192838:A:G; chr7:28149792:T:C; chr7:28152661:C:T; chr7:28156603:A:G; chr7:28154778:C:A; chr7:28184371:T:C; chr7:28184434:A:G; chr7:28216621:G:A; chr7:28140937:T:C; chr7:28180193:A:G; chr7:28156794:G:A; chr7:28159058:C:T; chr7:28160478:C:T; chr7:28147156:A:AT; chr7:28123055:C:T; chr7:28147492:A:ATTTT; chr7:28151111:ATTTTTT:ATTT; chr7:28139006:TG:T; chr7:28137719:G:Achr7:28184371:T:Ccoloc_sets:Y2_Y5:MergeCS1
In [10]:
# effect sign for each coloc sets
get_effect_sign_csets(cb_res)
$`coloc_sets:Y12_Y13_Y15:CS1`
A data.frame: 1 x 4
variantsAC_unproductiveDLPFC_unproductivePCC_unproductive
<chr><dbl><dbl><dbl>
chr7:27913416:A:Gchr7:27913416:A:G32.122179.71925526.30224
$`coloc_sets:Y1_Y4_Y8_Y16:CS2`
A data.frame: 9 x 5
variantsMicOPCACAD_Bellenguez_2022
<chr><dbl><dbl><dbl><dbl>
chr7:28137682:C:Tchr7:28137682:C:T28.19425-9.4862617.608747-5.610000
chr7:28118439:C:Tchr7:28118439:C:T28.19425-9.4862617.608747-5.590000
chr7:28117268:C:Tchr7:28117268:C:T28.19425-9.4862617.608747-5.580000
chr7:28136686:G:Achr7:28136686:G:A28.19425-9.4862617.608747-5.570000
chr7:28116987:C:Gchr7:28116987:C:G28.19425-9.4862617.608747-5.570000
chr7:28138643:G:Tchr7:28138643:G:T27.69204-9.3510937.777642-5.405941
chr7:28132564:A:Gchr7:28132564:A:G27.70500-9.4075597.705515-5.575758
chr7:28130784:T:Cchr7:28130784:T:C27.70500-9.4075597.705515-5.500000
chr7:28132395:C:Tchr7:28132395:C:T27.68988-9.3396207.776547-5.525253
$`coloc_sets:Y2_Y5:MergeCS1`
A data.frame: 20 x 3
variantsAstExc
<chr><dbl><dbl>
chr7:28192838:A:Gchr7:28192838:A:G 6.95853310.503492
chr7:28184371:T:Cchr7:28184371:T:C 6.85748210.586918
chr7:28184434:A:Gchr7:28184434:A:G 6.85748210.586918
chr7:28102567:G:Tchr7:28102567:G:T -7.238666-9.430452
chr7:28149792:T:Cchr7:28149792:T:C 6.824790 8.712003
chr7:28140937:T:Cchr7:28140937:T:C 6.733778 8.852091
chr7:28152661:C:Tchr7:28152661:C:T 6.798266 8.724166
chr7:28156603:A:Gchr7:28156603:A:G 6.798266 8.724166
chr7:28154778:C:Achr7:28154778:C:A 6.779118 8.704865
chr7:28151111:ATTTTTT:ATTTchr7:28151111:ATTTTTT:ATTT 6.561550 8.907106
chr7:28156794:G:Achr7:28156794:G:A 6.634914 8.919351
chr7:28159058:C:Tchr7:28159058:C:T 6.634914 8.919351
chr7:28160478:C:Tchr7:28160478:C:T 6.634914 8.919351
chr7:28147156:A:ATchr7:28147156:A:AT 6.617439 8.944349
chr7:28147492:A:ATTTTchr7:28147492:A:ATTTT 6.451539 8.936288
chr7:28137719:G:Achr7:28137719:G:A 6.469557 8.869312
chr7:28216621:G:Achr7:28216621:G:A 6.784733 9.530695
chr7:28139006:TG:Tchr7:28139006:TG:T 6.377519 8.871913
chr7:28180193:A:Gchr7:28180193:A:G 6.775521 9.370325
chr7:28123055:C:Tchr7:28123055:C:T 5.965627 8.839078
In [11]:
# LD between coloc sets
get_between_purity_simple(cb_res, gene.name = gene_id, path = '/data/colocalization/QTL_data/eQTL/')
A matrix: 3 x 5 of type chr
coloc_csets_1coloc_csets_2min_abs_cormax_abs_cormedian_abs_cor
coloc_sets:Y12_Y13_Y15:CS1 coloc_sets:Y1_Y4_Y8_Y16:CS20.05937818035624360.06850722796571540.0615616200035275
coloc_sets:Y12_Y13_Y15:CS1 coloc_sets:Y2_Y5:MergeCS1 0.04924894389405060.101409390070326 0.0897810753206947
coloc_sets:Y1_Y4_Y8_Y16:CS2coloc_sets:Y2_Y5:MergeCS1 0.528714321117617 0.718508216714854 0.554143837787159

Here, different colors refer to different 95% Colocalization Sets (CoS, a metric developed in ColocBoost indicating that there is 95% probabilty that this CoS captures a colocalization event). We only included ROSMAP data for this particular ColocBoost analysis. In this case, we observe cell specific eQTL, bulk sQTL colocalization on ROSMAP data with AD as two separate CoS, suggesting two putative causal signals. We did not detect colocalization with pQTL of statistical significance although from Section 1 there are some overlap with pQTL signals in fine-mapping CS, the overlapped variants in CS have small PIP.

Section 3: Refinement of colocalized loci with other AD GWAS¶

Here we refine the colocalization with other AD GWAS to iron out any heterogeniety between studies (heterogeniety can come from many sources), to get additional candidate loci from these more heterogenous sources as candidates to study.

In [12]:
AD_cohorts <- c('AD_Jansen_2021', 'AD_Bellenguez_EADB_2022', 'AD_Bellenguez_EADI_2022',
             'AD_Kunkle_Stage1_2019', 'AD_Wightman_Excluding23andMe_2021',
             'AD_Wightman_ExcludingUKBand23andME_2021', 'AD_Wightman_Full_2021')
cb_ad <- plot_cb(cb_res = cb_res, cex.pheno = 1.5, x.phen = -0.2, add_gwas = TRUE, gene_id = gene_id, cohorts = AD_cohorts)

No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.
No description has been provided for this image
In [13]:
pdf('plots/JAZF1/sec3.colocboost_res_allad.pdf', width = 10, height = 5)
replayPlot(cb_ad$p)
dev.off()
pdf: 2

Section 4: Assessment of multi-context xQTL effect sizes¶

Option 1: ColocBoost + MASH¶

Use colocboost variants and check for mash posterior contrast to see if the effect size are shared or specific or even opposite. Advantage is that colocboost result is AD GWAS informed; issue is that marginal posterior effects is not always the joint

Option 2: mvSuSiE¶

Use mvSuSiE multicontext fine-mapping results --- the bubble plot to check posterior effects. Issue is that we don't have this results yet, and this is limited to one cohort at a time, without information from AD.

We should go for option 1 by default and if we want to make claim about opposite effect size we double-check with mvSuSiE multicontext analysis.

In [93]:
message("Multi context in ROSMAP data")

multi_context_rosmap_tmp <- tryCatch(
    readRDS(paste0('/data/analysis_result/multi_context/ROSMAP/mnm/ROSMAP_DeJager.',
                   target_gene_info$gene_info$`#chr`, '_', gene_id, '.multicontext_bvsr.rds')),
    error = function(e) message('Error in loading ROSMAP multi context data')
)
if (!is.null(multi_context_rosmap_tmp[[1]]$mvsusie_fitted)) {
    plot_and_save(multi_context_rosmap_tmp[[1]], 'plots/JAZF1/sec4.multi_context_ROSMAP')
} else {
    message('Multi Context results are empty in ROSMAP data')
}
No description has been provided for this image
No description has been provided for this image
In [94]:
# Load and process MSBB data
message("Multi context in MSBB data")

multi_context_msbb_tmp <- tryCatch(
    readRDS(paste0('/data/analysis_result/multi_context/MSBB/mnm/MSBB_eQTL.',
                   target_gene_info$gene_info$`#chr`, '_', gene_id, '.multicontext_bvsr.rds')),
    error = function(e)  message('Error in loading MSBB multi context data')
)
if (!is.null(multi_context_msbb_tmp[[1]]$mvsusie_fitted)) {
    plot_and_save(multi_context_msbb_tmp[[1]], 'plots/JAZF1/sec4.multi_context_MSBB')
} else {
    message('Multi Context results are empty in MSBB data')
}

Section 5: Multi-context causal TWAS (including conventional TWAS and MR)¶

The most updated version of cTWAS analysis are under path s3://statfungen/ftp_fgc_xqtl/analysis_result/cTWAS/

TWAS results¶

We report TWAS from all contexts and methods from the pipeline. Here we will filter it down to the best performing methods and only keep contexts that are significant.

In [8]:
plot_TWAS_res(gene_id = gene_id, gene_name = gene_name)
No description has been provided for this image

MR results¶

This is only available for genes that are deemed significant in TWAS and have summary statistics available for effect size and standard errors in GWAS, in addition to z-scores --- current version does not support z-scores although we will soon also support z-scores in MR using MAF from reference panel.

cTWAS results¶

To be updated soon.

Section 6: Context specific multi-gene fine-mapping¶

A quick analysis: using the xQTL-AD summary table (flatten table)¶

We extract from xQTL-AD summary table the variants to get other genes also have CS with the variants shared by target gene and AD.

In [15]:
multigene_flat <- get_multigene_multicontext_flatten('Fungen_xQTL_allQTL.overlapped.gwas.export.JAZF1.rds', sQTL = 'no_MSBB')
multigene_flat
A data.frame: 23 x 6
gene_id#chrstartendgene_namecontexts
<chr><chr><int><int><chr><chr>
ENSG00000005020chr72699523826995239SKAP2 Inh_mega_eQTL,ROSMAP_DLPFC_sQTL,ROSMAP_PCC_sQTL
ENSG00000050344chr72615219726152198NFE2L3 MiGA_THA_eQTL
ENSG00000078399chr72717517927175180HOXA9 MiGA_GTS_eQTL
ENSG00000086300chr72629186126291862SNX10 MiGA_SVZ_eQTL,BM_10_MSBB_eQTL,ROSMAP_AC_sQTL
ENSG00000105928chr72475793924757940GSDME MiGA_GFM_eQTL,MiGA_GTS_eQTL
ENSG00000105991chr72709599927096000HOXA1 MiGA_SVZ_eQTL
ENSG00000106031chr72720009027200091HOXA13 MiGA_SVZ_eQTL
ENSG00000106049chr72766288227662883HIBADH MiGA_GTS_eQTL,MiGA_SVZ_eQTL,Oli_DeJager_eQTL,AC_DeJager_eQTL,Oli_Kellis_eQTL,Exc_mega_eQTL,Oli_mega_eQTL,ROSMAP_AC_sQTL,ROSMAP_PCC_sQTL
ENSG00000106052chr72773933027739331TAX1BP1 MiGA_SVZ_eQTL,ROSMAP_AC_sQTL,ROSMAP_DLPFC_sQTL
ENSG00000106066chr72919545029195451CPVL DLPFC_DeJager_eQTL,AC_DeJager_eQTL,DLPFC_Bennett_pQTL,DLPFC_Klein_gpQTL,ROSMAP_AC_sQTL,ROSMAP_DLPFC_sQTL
ENSG00000106069chr72914656829146569CHN2 MiGA_GTS_eQTL
ENSG00000106086chr73002740330027404PLEKHA8 STARNET_eQTL
ENSG00000122565chr72620116126201162CBX3 ROSMAP_AC_sQTL,ROSMAP_DLPFC_sQTL,STARNET_eQTL
ENSG00000122566chr72620148026201481HNRNPA2B1 MiGA_GTS_eQTL,ROSMAP_AC_sQTL
ENSG00000122592chr72715793527157936HOXA7 MiGA_GTS_eQTL,MiGA_THA_eQTL
ENSG00000136193chr72999028829990289SCRN1 MSBB_BM36_pQTL,ROSMAP_PCC_sQTL
ENSG00000146592chr72829932028299321CREB5 MiGA_SVZ_eQTL,MiGA_THA_eQTL,ROSMAP_AC_sQTL,ROSMAP_PCC_sQTL
ENSG00000153790chr72518035525180356C7orf31 MiGA_SVZ_eQTL
ENSG00000172115chr72512525925125260CYCS MiGA_SVZ_eQTL
ENSG00000176532chr72956383429563835PRR15 MiGA_SVZ_eQTL
ENSG00000255690chr72895832928958330TRIL MiGA_GTS_eQTL,BM_22_MSBB_eQTL
ENSG00000281039chr73055076030550761AC005154.5ROSMAP_PCC_sQTL,ROSMAP_DLPFC_sQTL
ENSG00000285162chr72912233929122340AC004593.2MiGA_SVZ_eQTL

Other genes implicated are PROC and HS6ST1 in MiGA cohort which may share causal eQTL with JAZF1. Further look into the data-set --- using these genes as targets and repeating what we did above for JAZF1 --- might be needed to establish a more certain conclusion.

Alternatively, we may be able to apply a multi-gene statistical fine-mapping test on JAZF1 region to find these genes, as you will see in the section below.

A statistically solid approach: mvSuSiE multi-gene analysis¶

This multi-gene fine-mapping analysis was done for each xQTL context separately. We will need to check the results for all contexts where this gene has an xQTL, in order to identify if there are other genes also sharing the same xQTL with this target gene. We included other genes in the same TAD window along with this gene, and extended it into a sliding window approach to include multiple TADs just in case. You need to check the sliding windows belongs to that gene (TSS) on analysis repo.

In [16]:
sliding_windows <- target_gene_info$gene_info$TADB_id %>% strsplit(., ',') %>% unlist %>% as.character
sliding_windows
  1. 'chr7_24118656_29243917'
  2. 'chr7_26830573_29825894'
  3. 'chr7_27953358_31892081'
In [97]:
mnm_gene_tmp <- readRDS('/data/analysis_result/multi_gene/ROSMAP/mnm_genes//ROSMAP_Mic_DeJager_eQTL.chr7_24118656_29243917.multigene_bvrs.rds')
In [100]:
mnm_gene_tmp[[1]]$mvsusie_fitted$condition_names
  1. 'ENSG00000105928'
  2. 'ENSG00000070882'
In [ ]:
ENSG00000105928: Chromosome 7: 24,698,355-24,757,940 reverse strand.
ENSG00000070882: Chromosome 7: 24,796,540-24,981,634 reverse strand.
JAZF1: Chromosome 7: 27,830,573-28,180,795
CPVL: Chromosome 7: 28,995,235-29,195,451 reverse strand.
In [103]:
mnm_gene_tmp <- readRDS('/data/analysis_result/multi_gene/ROSMAP/mnm_genes//ROSMAP_Mic_DeJager_eQTL.chr7_26830573_29825894.multigene_bvrs.rds')
In [104]:
mnm_gene_tmp[[1]]$mvsusie_fitted$condition_names

NULL
In [101]:
mnm_gene_tmp <- readRDS('/data/analysis_result/multi_gene/ROSMAP/mnm_genes//ROSMAP_Mic_DeJager_eQTL.chr7_27953358_31892081.multigene_bvrs.rds')
In [102]:
mnm_gene_tmp[[1]]$mvsusie_fitted$condition_names

NULL

The most updated version of mvSuSiE multi-gene results are under path s3://statfungen/ftp_fgc_xqtl/analysis_result/multi_gene/ROSMAP/mnm_genes/ Currently it is still WIP. You can revisit this later when we prompt you to. Here is an example for JAZF1:

In [105]:
# Main loop to process sliding windows
mnm_gene <- list()
for (window in sliding_windows) {
    context_files <- list.files('/data/analysis_result/multi_gene/ROSMAP/mnm_genes/', window, full.names = T) %>% .[str_detect(., '.multigene_bvrs.rds')]
    for(context_file in context_files){
        context_mnm = context_file %>% basename %>% str_split(., '[.]', simplify = T) %>% .[,1]
        # Load multi-gene data
        mnm_gene_tmp <- tryCatch(
            readRDS(context_file),
            error = function(e) NULL
        )
        
        if (!is.null(mnm_gene_tmp)) {
            # Check if target gene is in the condition names
            if (target_gene_info$gene_info$region_id %in% mnm_gene_tmp[[1]]$mvsusie_fitted$condition_names) {
                # Use a common prefix format for multi-gene plots
                plot_and_save(mnm_gene_tmp[[1]], 'plots/JAZF1/sec6.multigene')
            } else {
                message('There is mnm result for TAD window ', window, ' in ', context_mnm,
                        ', but it does not include target gene ', gene_name, ' in CS.')
            }
            # Append to the results list
            mnm_gene <- append(mnm_gene, list(mnm_gene_tmp))
        } 
    }
}

In this case, there is no statistical evidence for JAZF1 sharing any of its xQTL with other genes in ROSMAP Microglia data we looked into; although we have not analyzed MiGA this way yet (which showed some potential signals from the quick analysis above).

Section 7: Epigenomic QTL and their target regions¶

fsusie, see notebook

Generate a crude plot to determined whether the story is interesting¶

This is a crude version of the case study plot which shows the fsusie Effect (colored line), the gene body (black arrow), the epi-QTL (large dots with the same color as the effects) and ADGWAS cs position (small red dots).

Only produce the refine plot if we can see either:

  1. There are sharing snp between epi-QTL and AD CS
  2. There are the AD CS located within one of the effect range
  3. The crude plot suggest something interesting
In [9]:
options(repr.plot.width = 40, repr.plot.height = 40)

 ggplot() + theme_bw() + facet_grid(cs_coverage_0.95 + study + region ~ ., labeller = labeller(.rows = function(x) gsub("([_:,-])", "\n", x)), scale = "free_y") +

      theme(text = element_text(size = 20), strip.text.y = element_text(size = 25, angle = 0.5)) +
     # xlim(view_win) +
      ylab("Estimated effect") +
   #   geom_line(data = haQTL_df %>% mutate(study = "haQTL effect") %>% filter(CS == 5),
    #            aes_string(y = "fun_plot", x = "x", col = "CS"), size = 4, col = "#00AEEF") +
  geom_line(data = effect_of_interest ,
                aes_string(y = "fun_plot", x = "x", col = "cs_coverage_0.95"), size = 2) +  
    geom_point(data = effect_of_interest ,
                aes_string(y = "pip", x = "pos", col = "cs_coverage_0.95"), size = 10) +
    theme(text = element_text(size = 40), strip.text.y = element_text(size = 15, angle = 0.5), 
            axis.text.x = element_text(size = 40), axis.title.x = element_text(size = 40)) +
      xlab("Position") +
      ylab("Estimated\neffect") +
      geom_segment(arrow = arrow(length = unit(1, "cm")), aes(x = gene_start, xend = gene_end, y = 1, yend = 1), size = 6,
                  data = tar_gene_info$gene_info, alpha = 0.3) +
      geom_text(aes(x = (gene_start + gene_end) / 2, y = 1 , label = gene_name), size = 10, 
              data = tar_gene_info$gene_info)+
        geom_point(aes(x = pos, y = pip  ) ,color = "red", data = flatten_table%>%filter( str_detect(study,"AD_") , cs_coverage_0.95 != 0  )%>%mutate(AD_study = study%>%str_replace_all("_","\n" ))%>%select(-study,-region,-cs_coverage_0.95) )
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Section 8: Context focused validation in other xQTL data¶

see notebook

add fake version for now, so you don't have to refer to above link

Background: our "discovery set" is ROSMAP but we have additional "validation" sets including:

  • STARNET
  • MiGA
  • KnightADRC
  • MSBB
  • metaBrain
  • UKB pQTL

TODO:

  • Get from Carlos WashU CSF based resource (pQTL and metabolomic QTL)

This section shows verification of findings from these data-sets. In principle we should check them through sections 1-6 more formally. In practice we will start with colocalization via colocboost --- since our study is genetics (variant and loci level) focused. We can selectively follow them up for potentially intereting validations. We therefore only demonstrate validation via colocboost as a starting point.

In [19]:
finempping_contexts <- readRDS(paste0(gene_name, '_finemapping_contexts.rds')) # from sec1
In [20]:
finempping_contexts <- get_norosmap_contexts(finempping_contexts)
In [21]:
cb_ad <- plot_cb(cb_res = cb_res, cex.pheno = 1.5, x.phen = -0.2, add_QTL = TRUE, cohorts = finempping_contexts, gene_id = gene_id)

No pvalue cutoff. Extract all variants names.No pvalue cutoff. Extract all variants names.
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In conclusion from what's shown above, when we check the association signals in STARNET and MiGA on colocalization established from ROSMAP and AD GWAS, we see additional evidences.

Section 9: Non-linear effects of xQTL¶

see notebook

APOE interaction¶

In [9]:
options(repr.plot.width=6, repr.plot.height=6)

ggplot(JAZF1_int_res, aes(x = variant_id, y = qvalue_interaction)) +
  geom_point(alpha = 0.7, size = 6) +
  labs(title = "qvalue for JAZF1 csets in interaction association nalysis",
       x = "Gene Name",
       y = "qvalue_interaction",
       size = "qvalue_interaction") +
  theme_minimal(base_size = 14) +
  theme(panel.background = element_blank(),
        panel.grid.major = element_line(color = "grey80"),
        legend.position = NULL,
        axis.text.x = element_text(angle = 45, hjust = 1))  + ylim(0,1)
  # scale_color_manual(values = colorRampPalette(brewer.pal(8, "Set1"))(length(unique(flat_var$gene_name))))
ggsave('plots/JAZF1/sec11.interaction_association_JAZF1_lessPIP25.pdf', height = 5, width = 8)
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In conclusion, there is no interaction QTL with APOE identified.

Quantile QTL¶

Section 10: in silico functional studies in iPSC model¶

see notebook

In [11]:
vars_p
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In [13]:
apoe_p
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Section 11: Functional annotations of selected loci¶

see notebook

TODO

  • Touch base with Ryan on the snATAC annotations
  • Run this by Pavel to see if there are additional comments on how we do this
In [32]:
func_p
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Section 12: Candidate loci as trans-xQTL¶

see notebook

In [16]:
options(repr.plot.width=12, repr.plot.height=6)
if(!is.null(flat_var)){
    ggplot(flat_var, aes(x = gene_name, y = pip, size = pip)) +
      geom_point(alpha = 0.7) +
      labs(title = paste0("PIP values for trans fine mapped Genes in ", gene_name ," csets with AD"),
           x = "Gene Name",
           y = "PIP",
           size = "PIP",
           color = "CS Coverage 0.95 Min Corr") +
      theme_minimal(base_size = 14) +
      theme(panel.background = element_blank(),
            panel.grid.major = element_line(color = "grey80"),
            legend.position = NULL,
            axis.text.x = element_text(angle = 45, hjust = 1))  
      # scale_color_manual(values = colorRampPalette(brewer.pal(8, "Set1"))(length(unique(flat_var$gene_name))))
    ggsave(paste0('plots/JAZF1/sec12.trans_fine_mapping_',gene_name,'.pdf'), height = 5, width = 8)
} else{
    message('There are no detectable trans signals for ', gene_name)
}

Creative thinking: generate hypothesis, search in literature, raise questions to discuss¶

You can now generate some preliminary hypotheses based on the above results. Next, you should search for evidence in the literature to support or refine these hypotheses and identify additional analyses needed to confirm them.