analysis_plan.Rmd

---
title: "QGT-Columbia-analysis-plan"
author: "Hae Kyung Im"
contributors: "Owen Melia, Yanyu Liang, Tyson Miller"
date: "2020-06-10"
output: workflowr::wflow_html
editor_options:
  chunk_output_type: console
---

## Set up 

Linux is the operating system of choice to run bioinformatics software. We are offering two options

- Option 1: full setup, recommended for the linux-savvy with full setup
- Option 2: pre-installed RStudio in Google cloud, recommended for people less familiar with linux

The latest version of the analysis plan markdown document that generated this page is on [github here](https://github.com/hakyimlab/QGT-Columbia-HKI/blob/master/analysis/analysis_plan.Rmd)
rendered [here as an html page](https://hakyimlab.github.io/QGT-Columbia-HKI/analysis_plan.html)

# Option 1

- [ ] install anaconda/miniconda
- [ ] define imlabtools conda environment [how to here](https://github.com/hakyimlab/MetaXcan/blob/master/README.md#example-conda-environment-setup), which will install all the python modules needed for this analysis session
- [ ] download data and software [from Box](https://uchicago.box.com/s/zhapf2zfxcpj7thvq4sjnqale3emleum).
  This will have copies of all the software repositories and the models
- [x] download software (copies of the repos are already included in the course folder QCT-Columbia-HKI/repos/)
  - download metaxcan repo
  - download torus repo
  - download fastenloc repo
  - download TMWR repo
- [x] download prediction models from predictdb.org (a few models are included in the course folder QCT-Columbia-HKI/repos/)
- [ ] install R/RStudio/tidyverse package
- [ ] (optional) install workflowr package in R
- [ ] git clone https://github.com/hakyimlab/QGT-Columbia-HKI.git
- [ ] start Rstudio (if you installed workflowr, you can just open the QGT-Columbia-HKI.Rproj)

# Option 2
- [ ] claim your Rstudio server IP address and get the username and password [here](https://drive.google.com/file/d/1RNeOrOfORiS0PFuv4r0d6E2N5XE7I1tV/view?usp=sharing)
- [ ] connect to the Rstudio server using the url you claimed (http://xxx.xxx.xxx.xxx:8787) using a web browser
- [ ] log into the server using the username and password of the server you claimed

# Both options

## Summary of analysis plan

- predict whole blood expression
- check how well the prediction works with GEUVADIS expression data
- run association between predicted expression and a simulated phenotype
- calculate association between expression levels and coronary artery disease risk using s-predixcan
- fine-map the coronary artery disease gwas results using torus
- calculate colocalization probability using fastenloc
- run transcriptome-wide mendelian randomization in one locus of interestgi

## Initial remarks

- We ask you to actively participate in today's hands on activities. **Notice that we may ask you to share your screen for pedagogic purposes.**

- As you run the analysis and programs, we ask you to **respond the questions in [this document](https://drive.google.com/file/d/1RNeOrOfORiS0PFuv4r0d6E2N5XE7I1tV/view?usp=sharing).**
Find the tab with your name and fill out the questions as you go along.

- You are welcome to check other people's answers as guidelines but please make sure you write down your own answers.

- If you have any concerns about this, please ask me or one of the TAs for assistance. We are here to help you learn.

## Preliminary definitions

- [ ] Go to the terminal tab on the RStudio server and update the analysis document to the most recent version. The commands are shown below. Copy the text (without the lines with apostrophes: ```), paste them to the *terminal*, and hit enter.

```{bash eval=FALSE}
PRE="/home/student/"
cd $PRE/lab/
git pull 
```

- [ ] activate the the imlabtools environment, which will make sure all the necessary python modules are available to the software we will be running.
```{bash, eval=FALSE}
conda activate imlabtools
```

**Reminder: the bash chunks need to be copy-pasted to the terminal, not performed within the chunk.**

- [ ] execute the following chunk (you can use the green arrow below to the right)
```{r preliminary definitions, eval=FALSE}

suppressPackageStartupMessages(library(tidyverse))

```


- [ ] define some variables to access the data more easily within the R session. Run the following r chunk
```{r preliminaries, eval=FALSE}

print(getwd())

lab="/home/student/lab"
CODE=glue::glue("{lab}/code")
source(glue::glue("{CODE}/load_data_functions.R"))
source(glue::glue("{CODE}/plotting_utils_functions.R"))

PRE="/home/student/QGT-Columbia-HKI"
MODEL=glue::glue("{PRE}/models")
DATA=glue::glue("{PRE}/data")
RESULTS=glue::glue("{PRE}/results")
METAXCAN=glue::glue("{PRE}/repos/MetaXcan-master/software")
FASTENLOC=glue::glue("{PRE}/repos/fastenloc-master")
TORUS=glue::glue("{PRE}/repos/torus-master")
TWMR=glue::glue("{PRE}/repos/TWMR-master")

# This is a reference table we'll use a lot throughout the lab. It contains information about the genes.
gencode_df = load_gencode_df()
```

- [ ] define some variables to access the data more easily in the terminal. Run the following bash chunk. You will need to copy and paste the following chunk in the terminal


```{bash folder name variables, eval=FALSE}
export PRE="/home/student/QGT-Columbia-HKI"
export LAB="/home/student/lab"
export CODE=$LAB/code
export DATA=$PRE/data
export MODEL=$PRE/models
export RESULTS=$PRE/results
export METAXCAN=$PRE/repos/MetaXcan-master/software
export TWMR=$PRE/repos/TWMR-master
```

# Transcriptome-wide association methods
![Transcriptome-wide association methods](https://raw.githubusercontent.com/hakyimlab/QGT-Columbia-HKI/master/extras/figures/Association-Methods.png)

## predict expression 

![Visual summary of predixcan runs](https://raw.githubusercontent.com/hakyimlab/QGT-Columbia-HKI/master/extras/figures/PrediXcan-run.png)

- We will predict expression of genes in whole blood using the Predict.py code in the METAXCAN folder.

- Prediction models are located in the MODEL folder. Additional models for different tissues and transcriptome studies can be downloaded from [predictdb.org](http://predictdb.org)

- Remember you need to copy and paste this code chunk into the terminal to run it. Also make sure you activated the imlabtools environment which has all the necessary python modules. 

- Make sure all the paths and file names are correct

- This run should take about one minute.

- [ ] copy and paste the following block to the terminal and hit enter

```{bash predict genetic component of expression, eval=FALSE}

printf "Predict expression\n\n"
python3 $METAXCAN/Predict.py \
--model_db_path $PRE/models/gtex_v8_en/en_Whole_Blood.db \
--vcf_genotypes $DATA/predixcan/genotype/filtered.vcf.gz \
--vcf_mode genotyped \
--variant_mapping $DATA/predixcan/gtex_v8_eur_filtered_maf0.01_monoallelic_variants.txt.gz id rsid \
--on_the_fly_mapping METADATA "chr{}_{}_{}_{}_b38" \
--prediction_output $RESULTS/predixcan/Whole_Blood__predict.txt \
--prediction_summary_output $RESULTS/predixcan/Whole_Blood__summary.txt \
--verbosity 9 \
--throw

```


- [ ] check predicted values (run the following chunk using the green arrow)

```{r check prediction performance, eval=FALSE}

prediction_fp = glue::glue("{RESULTS}/predixcan/Whole_Blood__predict.txt")

## Read the Predict.py output into a dataframe. This function reorganizes the data and adds gene names.
predicted_expression = load_predicted_expression(prediction_fp, gencode_df)

head(predicted_expression)

## read summary of prediction, number of SNPs per gene, cross validated prediction performance
prediction_summary = load_prediction_summary(glue::glue("{RESULTS}/predixcan/Whole_Blood__summary.txt"), gencode_df)
## number of genes with a prediction model
dim(prediction_summary)
head(prediction_summary)

print("distribution of prediction performance r2")
summary(prediction_summary$pred_perf_r2)

```

## assess prediction performance (optional)

```{r assess prediction performance, eval=FALSE}

## download and read observed expression data from GEUVADIS 
## from https://uchicago.box.com/s/4y7xle5l0pnq9d1fwmthe2ewhogrnlrv

## Remove the version number from the gene_id's (ENSG000XXX.ver)
head(predicted_expression)

## merge predicted expression with observed expression data (by IID and gene)

## plot observes vs predicted expressioni for 
## ERAP1 (ENSG00000164307)
## PEX6 (ENSG00000124587)

## calculate spearman correlation for all genes

## what's the best performing gene?

```

## run association with a simulated phenotype

$Y = \sum_k T_k \beta_k + \epsilon$ 

with random effects $\beta_k \sim (1-\pi)\cdot \delta_0 + \pi\cdot N(0,1)$

```{bash run predixcan association, eval=FALSE}

export PHENO="sim.spike_n_slab_0.01_pve0.1"

printf "association\n\n"
python3 $METAXCAN/PrediXcanAssociation.py \
--expression_file $RESULTS/predixcan/Whole_Blood__predict.txt \
--input_phenos_file $DATA/predixcan/phenotype/$PHENO.txt \
--input_phenos_column pheno \
--output $RESULTS/predixcan/$PHENO/Whole_Blood__association.txt \
--verbosity 9 \
--throw

```

More predicted phenotypes can be [downloaded from here](https://uchicago.box.com/s/xxzuzjamscpc365ui9ge98le0qwy11wz). The naming of the phenotypes provides information about the genic architecture: the number after pve is the proportion of variance of Y explained by the genetic component of expression. The number after spike_n_slab represents the probability that a gene is causal $\pi$(i.e. prob $\beta \ne 0$)

## read association results

```{r read predixcan association results, eval=FALSE}

## read association results
PHENO="sim.spike_n_slab_0.01_pve0.1"

predixcan_association = load_predixcan_association(glue::glue("{RESULTS}/predixcan/{PHENO}/Whole_Blood__association.txt"),
                                                   gencode_df)

## take a look at the results
dim(predixcan_association)
predixcan_association %>% arrange(pvalue) %>% head
predixcan_association %>% arrange(pvalue) %>% ggplot(aes(pvalue)) + geom_histogram(bins=20)
## compare distribution against the null (uniform)
gg_qqplot(predixcan_association$pvalue, max_yval = 40)

```

## compare estimated effects with true effect sizes

```{r read true effect sizes, eval=FALSE}
truebetas = load_truebetas(glue::glue("{DATA}/predixcan/phenotype/gene-effects/{PHENO}.txt"), gencode_df)
betas = (predixcan_association %>% 
               inner_join(truebetas,by=c("gene"="gene_id")) %>%
               select(c('estimated_beta'='effect', 
                        'true_beta'='effect_size',
                        'pvalue', 
                        'gene_id'='gene', 
                        'gene_name'='gene_name.x', 
                        'region_id'='region_id.x')))
betas %>% arrange(pvalue) %>% head
## do you see examples of potential LD contamination?
betas %>% ggplot(aes(predicted_beta, true_beta))+geom_point()+geom_abline()
```


# Summary PrediXcan

Now we will use the summary results from a GWAS of coronary artery disease to calculate the association between the genetic component of the expression of genes and coronary artery disease risk. We will use the SPrediXcan.py.

![Visual summary of s-predixcan](https://raw.githubusercontent.com/hakyimlab/QGT-Columbia-HKI/master/extras/figures/gwas-PrediXcan-spredixcan.png)


- harmonized and imputed GWAS result for coronary artery disease is available in $PRE/spredixcan/data/

## run s-predixcan 

```{bash run s-predixcan, eval=FALSE}
python $METAXCAN/SPrediXcan.py \
--gwas_file  $DATA/spredixcan/imputed_CARDIoGRAM_C4D_CAD_ADDITIVE.txt.gz \
--snp_column panel_variant_id --effect_allele_column effect_allele --non_effect_allele_column non_effect_allele --zscore_column zscore \
--model_db_path $MODEL/gtex_v8_mashr/mashr_Whole_Blood.db \
--covariance $MODEL/gtex_v8_mashr/mashr_Whole_Blood.txt.gz \
--keep_non_rsid --additional_output --model_db_snp_key varID \
--throw \
--output_file $RESULTS/spredixcan/eqtl/CARDIoGRAM_C4D_CAD_ADDITIVE__PM__Whole_Blood.csv

```

## plot and interpret s-predixcan results

```{r analyze s-predixcan results, eval=FALSE}

spredixcan_association = load_spredixcan_association(glue::glue("{RESULTS}/spredixcan/eqtl/CARDIoGRAM_C4D_CAD_ADDITIVE__PM__Whole_Blood.csv"), gencode_df)
dim(spredixcan_association)
spredixcan_association %>% arrange(pvalue) %>% head
spredixcan_association %>% arrange(pvalue) %>% ggplot(aes(pvalue)) + geom_histogram(bins=20)

gg_qqplot(spredixcan_association$pvalue)

```

- [ ] SORT1, considered to be a causal gene for LDL cholesterol and as a consequence of coronary artery disease, is not found here. Why? (tissue)

## Exercise

- [ ] run s-predixcan with liver model, do you find SORT1? Is it significant?

- [ ] compare zscores in liver and whole blood.



## run multixcan (optional)

- multixcan aggregates information across multiple tissues to boost the power to detect association. It was developed movivated by the fact that eQTLs are shared across multiple tissues, i.e. many genetic variants that regulate expression are common across tissues.

```{bash run multixcan, eval=FALSE}
python $METAXCAN/SMulTiXcan.py \
--models_folder $MODEL/gtex_v8_mashr \
--models_name_pattern "mashr_(.*).db" \
--snp_covariance $MODEL/gtex_v8_expression_mashr_snp_smultixcan_covariance.txt.gz \
--metaxcan_folder $RESULTS/spredixcan/eqtl/ \
--metaxcan_filter "CARDIoGRAM_C4D_CAD_ADDITIVE__PM__(.*).csv" \
--metaxcan_file_name_parse_pattern "(.*)__PM__(.*).csv" \
--gwas_file $DATA/spredixcan/imputed_CARDIoGRAM_C4D_CAD_ADDITIVE.txt.gz \
--snp_column panel_variant_id --effect_allele_column effect_allele --non_effect_allele_column non_effect_allele --zscore_column zscore --keep_non_rsid --model_db_snp_key varID \
--cutoff_condition_number 30 \
--verbosity 7 \
--throw \
--output $RESULTS/smultixcan/eqtl/CARDIoGRAM_C4D_CAD_ADDITIVE_smultixcan.txt

```

# Colocalization methods

- Colocalization methods seek to estimate the probability that the complex trait and expression causal variants are the same. We favor methods that calculate the probability of causality for each trait (posterior inclusion probability), called fine-mapping methods. Here we use torus for fine-mapping and fastENLOC for colocalization.

![Visual summary of colocalization](https://raw.githubusercontent.com/hakyimlab/QGT-Columbia-HKI/master/extras/figures/colocalization-run.png)

## GWAS summary statistics to torus format

- the following code will format GWAS summary statistics into a format that the fine-mapping method torus can understand.

- we precalculated this for you so there is no need to recalculate

```{bash, eval=FALSE}
## notice that the GWAS results are in hg38
python $CODE/gwas_to_torus_zscore.py \
-input_gwas $DATA/spredixcan/imputed_CARDIoGRAM_C4D_CAD_ADDITIVE.txt.gz \
-input_ld_regions $DATA/spredixcan/eur_ld_hg38.txt.gz \
-output_fp $DATA/fastenloc/CARDIoGRAM_C4D_CAD_ADDITIVE.zval.gz
```

## fine-map GWAS results

- We will run torus due to time limitation but ideally we would like to run a method that allows multiple causal variants per locus, such as DAP-G or SusieR.

- torus has been precompiled and placed within the PATH

```{bash run torus, eval=FALSE}
export TORUSOFT=torus

$TORUSOFT -d $PRE/data/fastenloc/CARDIoGRAM_C4D_CAD_ADDITIVE.zval.gz --load_zval -dump_pip $PRE/data/fastenloc/CARDIoGRAM_C4D_CAD_ADDITIVE.gwas.pip
cd $PRE/data/fastenloc
gzip CARDIoGRAM_C4D_CAD_ADDITIVE.gwas.pip
cd $PRE 
```

We can take a quick look at the z-values and finemapping PIPs:

```{bash, eval=FALSE}
cd $PRE/data/fastenloc
zless CARDIoGRAM_C4D_CAD_ADDITIVE.zval.gz
zless CARDIoGRAM_C4D_CAD_ADDITIVE.gwas.pip.gz
```

## calculate colocalization with fastENLOC

```{bash run fastENLOC, eval=FALSE}
## check out tutorial https://github.com/xqwen/fastenloc/tree/master/tutorial

export eqtl_annotation_gzipped=$PRE/data/fastenloc/FASTENLOC-gtex_v8.eqtl_annot.vcf.gz
export gwas_data_gzipped=$PRE/data/fastenloc/CARDIoGRAM_C4D_CAD_ADDITIVE.gwas.pip.gz
export TISSUE=Whole_Blood
export FASTENLOCSOFT=fastenloc
##export FASTENLOCSOFT=/Users/owenmelia/projects/finemapping_bin/src/fastenloc/src/fastenloc

mkdir $RESULTS/fastenloc/
cd $RESULTS/fastenloc/
$FASTENLOCSOFT -eqtl $eqtl_annotation_gzipped -gwas $gwas_data_gzipped -t $TISSUE 

#[-total_variants total_snp] [-thread n] [-prefix prefix_name] [-s shrinkage]

```

## analyze results 

```{r analyze torus results, eval=FALSE}
## optional - compare with s-predixcan results

fastenloc_results = load_fastenloc_coloc_result(glue::glue("{RESULTS}/fastenloc/enloc.sig.out"))
spredixcan_and_fastenloc = inner_join(spredixcan_association, fastenloc_results, by=c('gene'='Signal'))
ggplot(spredixcan_and_fastenloc, aes(RCP, -log10(pvalue))) + geom_point()

## which genes are both colocalized (rcp>0.10) and significantly associated (pvalue<0.05/number of tests)


```

----------
# Mendelian randomization methods

## run  TWMR (for a locus)
![TWMR](https://raw.githubusercontent.com/hakyimlab/QGT-Columbia-HKI/master/extras/figures/TWMR.png)

```{bash run TWMR, eval=FALSE}

GENE=ENSG00000002919

cd $TWMR

R < $TWMR/MR.R --no-save $GENE

cd $PRE

## output: /home/student/QGT-Columbia-HKI/repos/TWMR-master/ENSG00000002919.alpha

```

```{r run TWMR, eval=FALSE}
# Load the 'analyseMR' function
source(glue::glue("{CODE}/TWMR_script.R"))

# Collect the list of genes available to run
gene_lst <- list.files(TWMR)
gene_lst <- gene_lst[str_detect(gene_lst, "ENS.*")]
gene_lst <- (gsub("\\..*", "", gene_lst) %>% unique)

# Set the gene and run. The function writes output to a file.
for (gene in gene_lst) {
  analyseMR(gene, TWMR)
}


```

```{r analyze TWMR results, eval=FALSE}

twmr_results <- load_twmr_results(TWMR, gencode_df)

```