---
title: "ANCOM-BC Tutorial"
author: 
  - Huang Lin$^1$
  - $^1$NICHD, 6710B Rockledge Dr, Bethesda, MD 20892
date: '`r format(Sys.Date(), "%B %d, %Y")`'
output: rmarkdown::html_vignette
bibliography: bibliography.bib
vignette: >
  %\VignetteIndexEntry{ANCOMBC}
  %\VignetteEngine{knitr::rmarkdown}
  \usepackage[utf8]{inputenc}
---

```{r setup, include = FALSE}
knitr::opts_chunk$set(message = FALSE, warning = FALSE, comment = NA, 
                      fig.width = 6.25, fig.height = 5)
library(ANCOMBC)
library(tidyverse)
library(DT)
options(DT.options = list(
  initComplete = JS("function(settings, json) {",
  "$(this.api().table().header()).css({'background-color': 
  '#000', 'color': '#fff'});","}")))
```

# 1. Introduction

Analysis of Compositions of Microbiomes with Bias Correction (ANCOM-BC) [@lin2020analysis] 
is a methodology of differential abundance (DA) analysis for microbial absolute
abundances. ANCOM-BC estimates the unknown sampling fractions, corrects 
the bias induced by their differences through a log linear regression model 
including the estimated sampling fraction as an offset terms, and identifies 
taxa that are differentially abundant according to the variable of interest. 
For more details, please refer to the 
[ANCOM-BC](https://doi.org/10.1038/s41467-020-17041-7) paper.

# 2. Installation

Download package. 

```{r getPackage, eval=FALSE}
if (!requireNamespace("BiocManager", quietly = TRUE))
    install.packages("BiocManager")
BiocManager::install("ANCOMBC")
```

Load the package. 

```{r load, eval=FALSE}
library(ANCOMBC)
```

# 3. Example Data

The HITChip Atlas dataset contains genus-level microbiota profiling with 
HITChip for 1006 western adults with no reported health complications, 
reported in [@lahti2014tipping]. The dataset is also available via the 
microbiome R package [@lahti2017tools] in phyloseq [@mcmurdie2013phyloseq] 
format. In this tutorial, we consider the following covariates:

* Continuous covariates: "age"

* Categorical covariates: "region", "bmi"

* The group variable of interest: "bmi"

    + Three groups: "lean", "overweight", "obese"
    
    + The reference group: "obese"

```{r}
data(atlas1006)

# Subset to baseline
tse = atlas1006[, atlas1006$time == 0]

# Re-code the bmi group
tse$bmi = recode(tse$bmi_group,
                 obese = "obese",
                 severeobese = "obese",
                 morbidobese = "obese")
# Subset to lean, overweight, and obese subjects
tse = tse[, tse$bmi %in% c("lean", "overweight", "obese")]

# Note that by default, levels of a categorical variable in R are sorted 
# alphabetically. In this case, the reference level for `bmi` will be 
# `lean`. To manually change the reference level, for instance, setting `obese`
# as the reference level, use:
tse$bmi = factor(tse$bmi, levels = c("obese", "overweight", "lean"))
# You can verify the change by checking:
# levels(sample_data(tse)$bmi)

# Create the region variable
tse$region = recode(as.character(tse$nationality),
                    Scandinavia = "NE", UKIE = "NE", SouthEurope = "SE", 
                    CentralEurope = "CE", EasternEurope = "EE",
                    .missing = "unknown")

# Discard "EE" as it contains only 1 subject
# Discard subjects with missing values of region
tse = tse[, ! tse$region %in% c("EE", "unknown")]

print(tse)
```

# 4 ANCOM-BC Implementation

## 4.1 Run ancombc function

```{r}
out = ancombc(data = tse, assay_name = "counts", 
              tax_level = "Family", phyloseq = NULL, 
              formula = "age + region + bmi", 
              p_adj_method = "holm", prv_cut = 0.10, lib_cut = 1000, 
              group = "bmi", struc_zero = TRUE, neg_lb = TRUE, tol = 1e-5, 
              max_iter = 100, conserve = TRUE, alpha = 0.05, global = TRUE,
              n_cl = 1, verbose = TRUE)

res = out$res
res_global = out$res_global

# ancombc also supports importing data in phyloseq format
# tse_alt = agglomerateByRank(tse, "Family")
# pseq = makePhyloseqFromTreeSummarizedExperiment(tse_alt)
# out = ancombc(data = NULL, assay_name = NULL,
#               tax_level = "Family", phyloseq = pseq,
#               formula = "age + region + bmi",
#               p_adj_method = "holm", prv_cut = 0.10, lib_cut = 1000,
#               group = "region", struc_zero = TRUE, neg_lb = TRUE, tol = 1e-5,
#               max_iter = 100, conserve = TRUE, alpha = 0.05, global = TRUE,
#               n_cl = 1, verbose = TRUE)
```

## 4.2 ANCOMBC primary result {.tabset}

Result from the ANCOM-BC log-linear model to determine taxa that are 
differentially abundant according to the covariate of interest. It contains: 
1) log fold changes; 2) standard errors; 3) test statistics; 4) p-values; 
5) adjusted p-values; 6) indicators whether the taxon is differentially 
abundant (TRUE) or not (FALSE).

### LFC

```{r}
tab_lfc = res$lfc
col_name = c("Taxon", "Intercept", "Age", "NE - CE", "SE - CE", 
             "US - CE", "Overweight - Obese", "Lean - Obese")
colnames(tab_lfc) = col_name
tab_lfc %>% 
  datatable(caption = "Log Fold Changes from the Primary Result") %>%
  formatRound(col_name[-1], digits = 2)
```

### SE

```{r}
tab_se = res$se
colnames(tab_se) = col_name
tab_se %>% 
  datatable(caption = "SEs from the Primary Result") %>%
  formatRound(col_name[-1], digits = 2)
```

### Test statistic

```{r}
tab_w = res$W
colnames(tab_w) = col_name
tab_w %>% 
  datatable(caption = "Test Statistics from the Primary Result") %>%
  formatRound(col_name[-1], digits = 2)
```

### P-values

```{r}
tab_p = res$p_val
colnames(tab_p) = col_name
tab_p %>% 
  datatable(caption = "P-values from the Primary Result") %>%
  formatRound(col_name[-1], digits = 2)
```

### Adjusted p-values

```{r}
tab_q = res$q
colnames(tab_q) = col_name
tab_q %>% 
  datatable(caption = "Adjusted p-values from the Primary Result") %>%
  formatRound(col_name[-1], digits = 2)
```

### Differentially abundant taxa

```{r}
tab_diff = res$diff_abn
colnames(tab_diff) = col_name
tab_diff %>% 
  datatable(caption = "Differentially Abundant Taxa from the Primary Result")
```

### Bias-corrected abundances

Step 1: obtain estimated sample-specific sampling fractions (in log scale). 

Step 2: correct the log observed abundances by subtracting the estimated 
sampling fraction from log observed abundances of each sample.

Note that we are only able to estimate sampling fractions up to an
additive constant. Thus, only the difference between bias-corrected abundances
are meaningful. 

```{r}
samp_frac = out$samp_frac
# Replace NA with 0
samp_frac[is.na(samp_frac)] = 0 
# Add pesudo-count (1) to avoid taking the log of 0
log_obs_abn = log(out$feature_table + 1)
# Adjust the log observed abundances
log_corr_abn = t(t(log_obs_abn) - samp_frac)
# Show the first 6 samples
round(log_corr_abn[, 1:6], 2) %>% 
  datatable(caption = "Bias-corrected log observed abundances")
```

### Visualization for age

```{r}
df_lfc = data.frame(res$lfc[, -1] * res$diff_abn[, -1], check.names = FALSE) %>%
    mutate(taxon_id = res$diff_abn$taxon) %>%
    dplyr::select(taxon_id, everything())
df_se = data.frame(res$se[, -1] * res$diff_abn[, -1], check.names = FALSE) %>% 
  mutate(taxon_id = res$diff_abn$taxon) %>%
    dplyr::select(taxon_id, everything())
colnames(df_se)[-1] = paste0(colnames(df_se)[-1], "SE")

df_fig_age = df_lfc %>% 
  dplyr::left_join(df_se, by = "taxon_id") %>%
  dplyr::transmute(taxon_id, age, ageSE) %>%
  dplyr::filter(age != 0) %>% 
  dplyr::arrange(desc(age)) %>%
  dplyr::mutate(direct = ifelse(age > 0, "Positive LFC", "Negative LFC"))
df_fig_age$taxon_id = factor(df_fig_age$taxon_id, levels = df_fig_age$taxon_id)
df_fig_age$direct = factor(df_fig_age$direct, 
                        levels = c("Positive LFC", "Negative LFC"))
  
p_age = ggplot(data = df_fig_age, 
           aes(x = taxon_id, y = age, fill = direct, color = direct)) + 
  geom_bar(stat = "identity", width = 0.7, 
           position = position_dodge(width = 0.4)) +
  geom_errorbar(aes(ymin = age - ageSE, ymax = age + ageSE), width = 0.2,
                position = position_dodge(0.05), color = "black") + 
  labs(x = NULL, y = "Log fold change", 
       title = "Log fold changes as one unit increase of age") + 
  scale_fill_discrete(name = NULL) +
  scale_color_discrete(name = NULL) +
  theme_bw() + 
  theme(plot.title = element_text(hjust = 0.5),
        panel.grid.minor.y = element_blank(),
        axis.text.x = element_text(angle = 60, hjust = 1))
p_age
```

### Visualization for BMI

```{r}
df_fig_bmi = df_lfc %>% 
  filter(bmioverweight != 0 | bmilean != 0) %>%
  transmute(taxon_id, 
            `Overweight vs. Obese` = round(bmioverweight, 2),
            `Lean vs. Obese` = round(bmilean, 2)) %>%
  pivot_longer(cols = `Overweight vs. Obese`:`Lean vs. Obese`, 
               names_to = "group", values_to = "value") %>%
  arrange(taxon_id)
lo = floor(min(df_fig_bmi$value))
up = ceiling(max(df_fig_bmi$value))
mid = (lo + up)/2
p_bmi = df_fig_bmi %>%
  ggplot(aes(x = group, y = taxon_id, fill = value)) + 
  geom_tile(color = "black") +
  scale_fill_gradient2(low = "blue", high = "red", mid = "white", 
                       na.value = "white", midpoint = mid, limit = c(lo, up),
                       name = NULL) +
  geom_text(aes(group, taxon_id, label = value), color = "black", size = 4) +
  labs(x = NULL, y = NULL, title = "Log fold changes as compared to obese subjects") +
  theme_minimal() +
  theme(plot.title = element_text(hjust = 0.5))
p_bmi
```

## 4.3 ANCOMBC global test result {.tabset}

Result from the ANCOM-BC global test to determine taxa that are 
differentially abundant between at least two groups across three or more 
different groups. In this example, we want to identify taxa that are 
differentially abundant between at least two regions across CE, NE, SE, and US.
The result contains: 1) test statistics; 2) p-values; 3) adjusted p-values; 
4) indicators whether the taxon is differentially abundant (TRUE) or not 
(FALSE).

### Test statistics

```{r}
tab_w = res_global[, c("taxon", "W")]
tab_w %>% datatable(caption = "Test Statistics 
                    from the Global Test Result") %>%
      formatRound(c("W"), digits = 2)
```

### P-values

```{r}
tab_p = res_global[, c("taxon", "p_val")]
tab_p %>% datatable(caption = "P-values 
                    from the Global Test Result") %>%
      formatRound(c("p_val"), digits = 2)
```

### Adjusted p-values

```{r}
tab_q = res_global[, c("taxon", "q_val")]
tab_q %>% datatable(caption = "Adjusted p-values 
                    from the Global Test Result") %>%
      formatRound(c("q_val"), digits = 2)
```

### Differentially abundant taxa

```{r}
tab_diff = res_global[, c("taxon", "diff_abn")]
tab_diff %>% datatable(caption = "Differentially Abundant Taxa 
                       from the Global Test Result")
```

### Visualization

```{r}
sig_taxa = res_global %>%
  dplyr::filter(diff_abn == TRUE) %>%
  .$taxon

df_bmi = tab_lfc %>%
    dplyr::select(Taxon, `Overweight - Obese`, `Lean - Obese`) %>%
    filter(Taxon %in% sig_taxa)

df_heat = df_bmi %>%
    pivot_longer(cols = -one_of("Taxon"),
                 names_to = "region", values_to = "value") %>%
    mutate(value = round(value, 2))
df_heat$Taxon = factor(df_heat$Taxon, levels = sort(sig_taxa))

lo = floor(min(df_heat$value))
up = ceiling(max(df_heat$value))
mid = (lo + up)/2
p_heat = df_heat %>%
  ggplot(aes(x = region, y = Taxon, fill = value)) + 
  geom_tile(color = "black") +
  scale_fill_gradient2(low = "blue", high = "red", mid = "white", 
                       na.value = "white", midpoint = mid, limit = c(lo, up),
                       name = NULL) +
  geom_text(aes(region, Taxon, label = value), color = "black", size = 4) +
  labs(x = NULL, y = NULL, 
       title = "Log fold changes for globally significant taxa") +
  theme_minimal() +
  theme(plot.title = element_text(hjust = 0.5))
p_heat
```

# Session information

```{r sessionInfo, message = FALSE, warning = FALSE, comment = NA}
sessionInfo()
```

# References









