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LJ_tfg-dge.R
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# Analysis of differential expression for temperature and Fe metatranscriptomics.
library(magrittr)
library(ggplot2)
library(beepr)
library(dplyr)
library(ggfortify)
library(testthat)
library(reshape2)
library(tidyverse)
library(edgeR)
library(gridExtra)
library(statmod)
# load group normalized data
#LJ can also do this for MCL data.. Import the MCL data, combine the cluster# and taxa to make clusters unique
#then change the name of the taxa.group column to grpnorm_taxgrp to fit in with the rest of this code.
#grp_norm <- read.csv("allMCL.csv")
#grp_norm$orf_id <- paste (grp_norm$cluster, grp_norm$Taxa.group)
#colnames(grp_norm)[1] <- "grpnorm_taxgrp"
grp_norm <- read.csv("annotation_allTFG.grpnorm_mmetsp_fc_pn_reclassified.edgeR.csv")
grp_norm <- dplyr::filter (grp_norm, grepl('Pseudo-nit|Fragilariopsis',grpnorm_taxgrp))
# read in experiment key with associated treatments
tfg_key <- read.csv("tfg_key.csv")
tfg_key2 <- tfg_key %>%
dplyr::filter(time == 5 | time == 0,
b12 != 1 | is.na(b12))
# subset large original dataframe
grp_norm_sub <- grp_norm %>% dplyr::select('orf_id',# 'group',
'grpnorm_taxgrp', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C', 'TFG_t0_A',
'TFG_t0_B', 'TFG_t0_C')
#LJ -subset only frag and pseudo-nit. this is only for tfg paper that I'm doing.
#grp_norm_sub <- dplyr::filter (grp_norm_sub, grepl('Pseudo-nit|Fragilariopsis',grpnorm_taxgrp))
grp_norm_sub_not0 <- grp_norm %>% dplyr::select('orf_id',# 'group',
'grpnorm_taxgrp', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C')
# change the row names to be the ORF ID
rownames(grp_norm_sub) <- grp_norm_sub$orf_id
# combine the expression values all into one column, with each referring to a sample ID
grp_norm_t <- melt(grp_norm_sub, variable.name = 'sample_key',
value.name = 'expression_value') %>%
inner_join(y = tfg_key, by = 'sample_key')
# read in normalization factors
norm_factors <- read.csv("norm_factors_mmetsp_fc_pn_reclassified.csv")
norm_factors_sub <- norm_factors %>% dplyr::select('group', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C')
# making a dataframe of taxon specific normalization factors
tax_specific_abundance_norms <- data.frame(grpnorm_taxgrp = norm_factors$group,
norm_factors_group = rowMeans(norm_factors_sub[,c(2:ncol(norm_factors_sub))]))
# grouping of treatments
samples_present <- inner_join(x = data.frame(sample_key = names(grp_norm_sub_not0)[3:23]),
y = tfg_key, by = 'sample_key')
treatment_groups <- paste(samples_present$temp, samples_present$fe)
## multiplying abundance scaling factors
grp_norm_sub_not0 <- inner_join(x = grp_norm_sub_not0,
y = tax_specific_abundance_norms,
by = 'grpnorm_taxgrp')
grp_norm_sub_scaled <- grp_norm_sub_not0[c(3:20)]*grp_norm_sub_not0$norm_factors_group
# making a 'DGE List' for edgeR differential expression analysis
dge_list_tfg <- DGEList(counts = grp_norm_sub_scaled,
group = treatment_groups,
remove.zeros = FALSE,
genes = grp_norm_sub_not0$orf_id)
## used for old analysis with traditional model formulation
# fe <- as.logical(samples_present$fe)
# temperature_factor <- as.factor(temperature)
groups <- paste('fe', samples_present$fe, 'temp', samples_present$temp, sep = '_')
groups <- gsub(pattern = "-", replacement = "", x = groups)
# model matrix with each individual group as a unique factor
tfg_mm_factors <- model.matrix(~0 + groups)
# tfg_mm_contin is the old model formulation
# tfg_mm_contin <- model.matrix(~fe*temperature_factor)
# estimating dispersion parameters
tfg_disp_factors <- estimateGLMCommonDisp(dge_list_tfg,
design = tfg_mm_factors)
# tfg_disp_contin <- estimateGLMCommonDisp(dge_list_tfg,
# design = tfg_mm_contin)
# fitting gene-wise models
tfg_fit_factors <- glmQLFit(tfg_disp_factors, design = tfg_mm_factors, robust = TRUE)
# tfg_fit_contin <- glmQLFit(tfg_disp_contin, design = tfg_mm_contin, robust = TRUE)
# quasi likelihood DE test
# setting up contrasts to look at fe, temp, and interactions. See these links for guidance:
# for contrast formulation of temp_3vstemp_05:
# https://support.bioconductor.org/p/80224/
# for guidance on setting up model contrasts, see section 'Complicated Contrasts'
#https://bioconductor.org/packages/release/workflows/vignettes/RnaSeqGeneEdgeRQL/inst/doc/edgeRQL.html
# for discussion about using contrasts over traditional model formulation:
# https://support.bioconductor.org/p/115795/#115831
# the first set of contrasts are pairwise contrasts.
my_contrasts <- makeContrasts(fe0_temp3vstemp05 = groupsfe_0_temp_3 - groupsfe_0_temp_0.5,
fe0_temp6vstemp05 = groupsfe_0_temp_6 - groupsfe_0_temp_0.5,
fe0_temp6vstemp3 = groupsfe_0_temp_6 - groupsfe_0_temp_3,
fe2_temp3vstemp05 = groupsfe_2_temp_3 - groupsfe_2_temp_0.5,
fe2_temp6vstemp05 = groupsfe_2_temp_6 - groupsfe_2_temp_0.5,
fe2_temp6vstemp3 = groupsfe_2_temp_6 - groupsfe_2_temp_3,
# Fe pairwise comparisons
temp05_fe2vsfe0 = groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5,
temp3_fe2vsfe0 = groupsfe_2_temp_3 - groupsfe_0_temp_3,
temp6_fe2vsfe0 = groupsfe_2_temp_6 - groupsfe_0_temp_6,
# fe_all contrast: all the coefficients associated with iron compared with those without iron. testing overall expression of +Fe treatments
fe_all = (groupsfe_2_temp_0.5 + groupsfe_2_temp_3 + groupsfe_2_temp_6 - groupsfe_0_temp_0.5 - groupsfe_0_temp_3 - groupsfe_0_temp_6)/3,
# testing overall expression of Temp 3 treatments compared with temp 0.5
temp_3vstemp_05 = ((groupsfe_2_temp_3 - groupsfe_2_temp_0.5) + (groupsfe_0_temp_3 - groupsfe_0_temp_0.5))/2,
# testing overall expression of Temp 6 treatments compared with temp 0.5
temp_6vstemp_05 = ((groupsfe_2_temp_6 - groupsfe_2_temp_0.5) + (groupsfe_0_temp_6 - groupsfe_0_temp_0.5))/2,
# testing overall expression fo Temp 6 treatments compared with temp 3
temp_6vstemp_3 = ((groupsfe_2_temp_6 - groupsfe_2_temp_3) + (groupsfe_0_temp_6 - groupsfe_0_temp_3))/2,
# testing interaction between temp and iron, between temps 6 and 0.5
tempfe_interaction_temp_6vstemp_05 = (groupsfe_2_temp_6 - groupsfe_0_temp_6) - (groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5),
# testing interaction between temp and iron, between temps 6 and 0.5
tempfe_interaction_temp_3vstemp_05 = (groupsfe_2_temp_3 - groupsfe_0_temp_3) - (groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5),
levels = tfg_mm_factors)
# pairwise comparisons
# temperature pairwise comparisons
# low iron
fe0_temp3vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp3vstemp05'])
fe0_temp6vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp6vstemp05'])
fe0_temp6vstemp3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp6vstemp3'])
# high iron
fe2_temp3vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp3vstemp05'])
fe2_temp6vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp6vstemp05'])
fe2_temp6vstemp3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp6vstemp3'])
# fe pairwise comparisons
temp05_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp05_fe2vsfe0'])
temp3_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp3_fe2vsfe0'])
temp6_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp6_fe2vsfe0'])
# overall Fe DE values testing
fe_all_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe_all'])
# temperature comparison values
temp_3vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_3vstemp_05'])
temp_6vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_6vstemp_05'])
temp_6vstemp_3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_6vstemp_3'])
#temperature and Fe 'interaction' values
tempfe_interaction_temp_6vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'tempfe_interaction_temp_6vstemp_05'])
tempfe_interaction_temp_3vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'tempfe_interaction_temp_3vstemp_05'])
# function for processing topTags() output that spits out the logFC and adjusted p value
out_toptag <- function(qlf_test_output){
# qlf_test_output <- fe_all_test
top_out <- topTags(qlf_test_output, n = Inf, adjust.method = 'BH', sort.by = 'none')
# get name of input
nm <- deparse(substitute(qlf_test_output))
nm_adj <- gsub(pattern = "_test", replacement = "", x = nm)
# making the foldchange and p value columns
foldchange <- top_out[[1]]$logFC
pvalue <- top_out[[1]]$FDR
result_df <- data.frame(foldchange, pvalue)
#adjusting names so that they have the test name appended with 'pvalue' and 'foldchange'
names(result_df) <- paste0(nm_adj, "_", names(result_df))
return(result_df)
}
## up / down / none decisions about DE genes
# pairwise comparisons
# temperature comparisons:
# low iron
fe0_temp3vstemp05_decide <- decideTestsDGE(fe0_temp3vstemp05_test)
fe0_temp3vstemp05_info <- out_toptag(fe0_temp3vstemp05_test)
fe0_temp6vstemp05_decide <- decideTestsDGE(fe0_temp6vstemp05_test)
fe0_temp6vstemp05_info <- out_toptag(fe0_temp6vstemp05_test)
fe0_temp6vstemp3_decide <- decideTestsDGE(fe0_temp6vstemp3_test)
fe0_temp6vstemp3_info <- out_toptag(fe0_temp6vstemp3_test)
# high iron
fe2_temp3vstemp05_decide <- decideTestsDGE(fe2_temp3vstemp05_test)
fe2_temp3vstemp05_info <- out_toptag(fe2_temp3vstemp05_test)
fe2_temp6vstemp05_decide <- decideTestsDGE(fe2_temp6vstemp05_test)
fe2_temp6vstemp05_info <- out_toptag(fe2_temp6vstemp05_test)
fe2_temp6vstemp3_decide <- decideTestsDGE(fe2_temp6vstemp3_test)
fe2_temp6vstemp3_info <- out_toptag(fe2_temp6vstemp3_test)
# fe pairwise comparisons
temp05_fe2vsfe0_decide <- decideTestsDGE(temp05_fe2vsfe0_test)
temp05_fe2vsfe0_info <- out_toptag(temp05_fe2vsfe0_test)
temp3_fe2vsfe0_decide <- decideTestsDGE(temp3_fe2vsfe0_test)
temp3_fe2vsfe0_info <- out_toptag(temp3_fe2vsfe0_test)
temp6_fe2vsfe0_decide <- decideTestsDGE(temp6_fe2vsfe0_test)
temp6_fe2vsfe0_info <- out_toptag(temp6_fe2vsfe0_test)
# Fe decision
fe_all_decide <- decideTestsDGE(fe_all_test)
fe_all_info <- out_toptag(fe_all_test)
# Temperature decision
temp_3vstemp_05_decide <- decideTestsDGE(temp_3vstemp_05_test)
temp_3vstemp_05_info <- out_toptag(temp_3vstemp_05_test)
temp_6vstemp_05_decide <- decideTestsDGE(temp_6vstemp_05_test)
temp_6vstemp_05_info <- out_toptag(temp_6vstemp_05_test)
temp_6vstemp_3_decide <- decideTestsDGE(temp_6vstemp_3_test)
temp_6vstemp_3_info <- out_toptag(temp_6vstemp_3_test)
# interaction DE decision
tempfe_interaction_temp_6vstemp_05_decide <- decideTestsDGE(tempfe_interaction_temp_6vstemp_05_test)
tempfe_interaction_temp_6vstemp_05_info <- out_toptag(tempfe_interaction_temp_6vstemp_05_test)
tempfe_interaction_temp_3vstemp_05_decide <- decideTestsDGE(tempfe_interaction_temp_3vstemp_05_test)
tempfe_interaction_temp_3vstemp_05_info <- out_toptag(tempfe_interaction_temp_3vstemp_05_test)
# checking total number of DE genes for each test
# [email protected] %>% abs() %>% sum()
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# getting only the rows which do not have na for grpnorm_taxgrp
#grp_norm_no_grp_na <- grp_norm[!is.na(grp_norm$grpnorm_taxgrp),]
#LJ changed the line above into this because I didn't have any NA values
grp_norm_no_grp_na <- dplyr::filter (grp_norm, !grepl('^$', grpnorm_taxgrp))
# dataframe with actual values used for DE analysis (transformed vals by tax-specific scaling factor)
grp_norm_sub_scaled_copy <- grp_norm_sub_scaled
names(grp_norm_sub_scaled_copy) <- paste0(names(grp_norm_sub_scaled_copy), '-scaled')
## making compiled dataframe
tfg_de_df <- data.frame(Fe_vs_noFe_de = fe_all_decide %>% as.vector(),
Fe_vs_noFe_pvalue = fe_all_info$fe_all_pvalue,
Fe_vs_noFe_foldchange = fe_all_info$fe_all_foldchange,
# temperature comparisons
temp_3C_vs_0C_de = temp_3vstemp_05_decide %>% as.vector(),
temp_3C_vs_0C_pvalue = temp_3vstemp_05_info$temp_3vstemp_05_pvalue,
temp_3C_vs_0C_foldchange = temp_3vstemp_05_info$temp_3vstemp_05_foldchange,
temp_6C_vs_0C_de = temp_6vstemp_05_decide %>% as.vector(),
temp_6C_vs_0C_pvalue = temp_6vstemp_05_info$temp_6vstemp_05_pvalue,
temp_6C_vs_0C_foldchange = temp_6vstemp_05_info$temp_6vstemp_05_foldchange,
temp_6C_vs_3C_de = temp_6vstemp_3_decide %>% as.vector(),
temp_6C_vs_3C_pvalue = temp_6vstemp_3_info$temp_6vstemp_3_pvalue,
temp_6C_vs_3C_foldchange = temp_6vstemp_3_info$temp_6vstemp_3_foldchange,
int_fe_temp_6C_vs_0C_de = tempfe_interaction_temp_6vstemp_05_decide %>% as.vector(),
int_fe_temp_6C_vs_0C_pvalue = tempfe_interaction_temp_6vstemp_05_info$tempfe_interaction_temp_6vstemp_05_pvalue,
int_fe_temp_6C_vs_0C_foldchange = tempfe_interaction_temp_6vstemp_05_info$tempfe_interaction_temp_6vstemp_05_foldchange,
int_fe_temp_3C_vs_0C_de = tempfe_interaction_temp_3vstemp_05_decide %>% as.vector(),
int_fe_temp_3C_vs_0C_pvalue = tempfe_interaction_temp_3vstemp_05_info$tempfe_interaction_temp_3vstemp_05_pvalue,
int_fe_temp_3C_vs_0C_foldchange = tempfe_interaction_temp_3vstemp_05_info$tempfe_interaction_temp_3vstemp_05_foldchange,
# pairwise comparisons
noFe_3C_vs_noFe_0C_de = fe0_temp3vstemp05_decide %>% as.vector(),
noFe_3C_vs_noFe_0C_pvalue = fe0_temp3vstemp05_info$fe0_temp3vstemp05_pvalue,
noFe_3C_vs_noFe_0C_foldchange = fe0_temp3vstemp05_info$fe0_temp3vstemp05_foldchange,
Fe_3C_vs_Fe_0C_de = fe2_temp3vstemp05_decide %>% as.vector(),
Fe_3C_vs_Fe_0C_pvalue = fe2_temp3vstemp05_info$fe2_temp3vstemp05_pvalue,
Fe_3C_vs_Fe_0C_foldchange = fe2_temp3vstemp05_info$fe2_temp3vstemp05_foldchange,
noFe_6C_vs_noFe_0C_de = fe0_temp6vstemp05_decide %>% as.vector(),
noFe_6C_vs_noFe_0C_pvalue = fe0_temp6vstemp05_info$fe0_temp6vstemp05_pvalue,
noFe_6C_vs_noFe_0C_foldchange = fe0_temp6vstemp05_info$fe0_temp6vstemp05_foldchange,
Fe_6C_vs_Fe_0C_de = fe2_temp6vstemp05_decide %>% as.vector(),
Fe_6C_vs_Fe_0C_pvalue = fe2_temp6vstemp05_info$fe2_temp6vstemp05_pvalue,
Fe_6C_vs_Fe_0C_foldchange = fe2_temp6vstemp05_info$fe2_temp6vstemp05_foldchange,
noFe_6C_vs_noFe_3C_de = fe0_temp6vstemp3_decide %>% as.vector(),
noFe_6C_vs_noFe_3C_pvalue = fe0_temp6vstemp3_info$fe0_temp6vstemp3_pvalue,
noFe_6C_vs_noFe_3C_foldchange = fe0_temp6vstemp3_info$fe0_temp6vstemp3_foldchange,
Fe_6C_vs_Fe_3C_de = fe2_temp6vstemp3_decide %>% as.vector(),
Fe_6C_vs_Fe_3C_pvalue = fe2_temp6vstemp3_info$fe2_temp6vstemp3_pvalue,
Fe_6C_vs_Fe_3C_foldchange = fe2_temp6vstemp3_info$fe2_temp6vstemp3_foldchange,
Fe_0C_vs_noFe_0C_de = temp05_fe2vsfe0_decide %>% as.vector(),
Fe_0C_vs_noFe_0C_pvalue = temp05_fe2vsfe0_info$temp05_fe2vsfe0_pvalue,
Fe_0C_vs_noFe_0C_foldchange = temp05_fe2vsfe0_info$temp05_fe2vsfe0_foldchange,
Fe_3C_vs_noFe_3C_de = temp3_fe2vsfe0_decide %>% as.vector(),
Fe_3C_vs_noFe_3C_pvalue = temp3_fe2vsfe0_info$temp3_fe2vsfe0_pvalue,
Fe_3C_vs_noFe_3C_foldchange = temp3_fe2vsfe0_info$temp3_fe2vsfe0_foldchange,
Fe_6C_vs_noFe_6C_de = temp6_fe2vsfe0_decide %>% as.vector(),
Fe_6C_vs_noFe_6C_pvalue = temp6_fe2vsfe0_info$temp6_fe2vsfe0_pvalue,
Fe_6C_vs_noFe_6C_foldchange = temp6_fe2vsfe0_info$temp6_fe2vsfe0_foldchange,
# including dataframe with annotations
grp_norm_no_grp_na,
# including scaled values,
grp_norm_sub_scaled_copy,
# columns for plotting DE analysis
fe_neg_de = ifelse(fe_all_decide == -1, yes = -1, no = 0) %>% as.vector(),
fe_pos_de = ifelse(fe_all_decide == 1, yes = 1, no = 0) %>% as.vector(),
# temperature is a bit harder than Fe. The gene has to be DE in either comparisons from 3vs0.5 *or* 6vs0.5 to be counted in this column. But if the gene is negatively expressed from 3vs0.5, and positively expressed from 6vs0.5, it would be excluded.
temp_neg_de = ifelse((temp_3vstemp_05_decide == -1 | temp_6vstemp_05_decide == -1) &
(temp_3vstemp_05_decide != 1 | temp_6vstemp_05_decide != 1),
yes = -1, no = 0) %>% as.vector(),
temp_pos_de = ifelse((temp_3vstemp_05_decide == 1 | temp_6vstemp_05_decide == 1) &
(temp_3vstemp_05_decide != -1 | temp_6vstemp_05_decide != -1),
yes = 1, no = 0) %>% as.vector(),
tempfe_neg_de = ifelse((tempfe_interaction_temp_6vstemp_05_decide == -1 | tempfe_interaction_temp_3vstemp_05_decide == -1) &
(tempfe_interaction_temp_6vstemp_05_decide != 1 & tempfe_interaction_temp_3vstemp_05_decide != 1),
yes = -1, no = 0) %>% as.vector(),
tempfe_pos_de = ifelse((tempfe_interaction_temp_6vstemp_05_decide == 1 | tempfe_interaction_temp_3vstemp_05_decide == 1) &
(tempfe_interaction_temp_6vstemp_05_decide != -1 & tempfe_interaction_temp_3vstemp_05_decide != -1),
yes = 1, no = 0) %>% as.vector(),
# abs_fe is for ranking taxonomic groups for plotting later on.
abs_fe = ifelse(abs(fe_all_decide) == 1, yes = 1, no = 0) %>% as.vector())
# old analysis
# fe0_temp05vs3 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp05vstemp3'])
# fe0_temp05vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp05vstemp6'])
# fe0_temp3vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp3vstemp6'])
#
# fe2_temp05vs3 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp05vstemp3'])
# fe2_temp05vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp05vstemp6'])
# fe2_temp3vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp3vstemp6'])
#
#
# fe0_temp05vs3_decide <- decideTestsDGE(object = fe0_temp05vs3)
# fe0_temp05vs6_decide <- decideTestsDGE(object = fe0_temp05vs6)
# fe0_temp3vs6_decide <- decideTestsDGE(object = fe0_temp3vs6)
#
# fe2_temp05vs3_decide <- decideTestsDGE(object = fe2_temp05vs3)
# fe2_temp05vs6_decide <- decideTestsDGE(object = fe2_temp05vs6)
# fe2_temp3vs6_decide <- decideTestsDGE(object = fe2_temp3vs6)
#
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
## getting significance tests of old model formulation
tfg_inter <- glmQLFTest(tfg_fit_contin, coef = 1)
tfg_fe <- glmQLFTest(tfg_fit_contin, coef = 2)
tfg_temp3 <- glmQLFTest(tfg_fit_contin, coef = 3)
tfg_temp6 <- glmQLFTest(tfg_fit_contin, coef = 4)
tfg_fetemp3 <- glmQLFTest(tfg_fit_contin, coef = 5)
tfg_fetemp6 <- glmQLFTest(tfg_fit_contin, coef = 6)
#
# tfg_inter_decide <- decideTestsDGE(tfg_inter)
# tfg_fe_decide <- decideTestsDGE(tfg_fe)
# tfg_temp3_decide <- decideTestsDGE(tfg_temp3)
# tfg_temp6_decide <- decideTestsDGE(tfg_temp6)
# tfg_fetemp3_decide <- decideTestsDGE(tfg_fetemp3)
# tfg_fetemp6_decide <- decideTestsDGE(tfg_fetemp6)
### old version writing final dataframe
# tfg_de_df <- data.frame(tfg_inter_decide, tfg_fe_decide, tfg_temp3_decide,
# tfg_temp6_decide, tfg_fetemp3_decide, tfg_fetemp6_decide,
# grp_norm_sub_not0,
# abs_fe = ifelse(abs(tfg_fe_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# abs_temp = ifelse(abs(tfg_temp3_decide) == 1 | abs(tfg_temp6_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# abs_tempfe = ifelse(abs(tfg_fetemp3_decide) == 1 | abs(tfg_fetemp6_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# # summaries of negative DE by treatment *group*
# fe_neg_de = ifelse((tfg_fe_decide == -1 | tfg_fe_decide == -1) &
# (tfg_fe_decide != 1 | tfg_fe_decide!= 1), yes = -1, no = 0) %>% as.vector(),
# temp_neg_de = ifelse((tfg_temp3_decide == -1 | tfg_temp6_decide == -1) &
# (tfg_temp3_decide != 1 | tfg_temp6_decide!= 1), yes = -1, no = 0) %>% as.vector(),
# fetemp_neg_de = ifelse((tfg_fetemp3_decide == -1 | tfg_fetemp6_decide == -1) &
# (tfg_fetemp3_decide != 1 | tfg_fetemp6_decide!= 1), yes = -1, no = 0) %>% as.vector(),
#
# # summaries of positive DE by treatment *group*
# fe_pos_de = ifelse((tfg_fe_decide == 1 | tfg_fe_decide == 1) &
# (tfg_fe_decide != -1 | tfg_fe_decide!= -1), yes = 1, no = 0) %>% as.vector(),
# temp_pos_de = ifelse((tfg_temp3_decide == 1 | tfg_temp6_decide == 1) &
# (tfg_temp3_decide != -1 | tfg_temp6_decide!= -1), yes = 1, no = 0) %>% as.vector(),
# fetemp_pos_de = ifelse((tfg_fetemp3_decide == 1 | tfg_fetemp6_decide == 1) &
# (tfg_fetemp3_decide != -1 | tfg_fetemp6_decide!= -1), yes = 1, no = 0) %>% as.vector())
write.csv(tfg_de_df, file = 'tfg_de_annotation_frag_pseudoTFG.grpnorm_mmetsp_fc_pn_reclassified.csv')
### plotting de results by taxon
# blank plot just used for the axis.
blank_p <- tfg_de_df %>%
group_by(grpnorm_taxgrp) %>%
summarise(fe_grp = sum(abs_fe)) %>%
ggplot(aes(x = fe_grp,
y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
# geom_point() +
theme_bw() +
xlab('') +
theme(axis.text.x = element_text(colour = 'white'),
panel.grid.major.x = element_blank(),
panel.grid.minor.x = element_blank(),
axis.ticks = element_blank()) +
ylab('');blank_p
# old plots that show total DE, not subdivided into positive and negative DE:
# p1_fe <- tfg_de_df %>%
# group_by(grpnorm_taxgrp) %>%
# summarise(fe_grp = sum(abs_fe)) %>%
# ggplot(aes(x = fe_grp, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
# geom_point(size = 3, alpha = 0.5) +
# theme_bw() +
# xlab('Iron-Related DE') +
# ylab('') +
# theme(axis.text.y = element_blank());p1_fe
#
# p2_temp <- tfg_de_df %>%
# group_by(grpnorm_taxgrp) %>%
# summarise(fe_grp = sum(abs_fe),
# temp_grp = sum(abs_temp)) %>%
# ggplot(aes(x = temp_grp, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
# geom_point(size = 3, alpha = 0.5) +
# theme_bw() +
# ylab('') +
# xlab('Temperature-Related DE') +
# theme(axis.text.y = element_blank());p2_temp
#
# p3_tempfe <- tfg_de_df %>%
# group_by(grpnorm_taxgrp) %>%
# summarise(fe_grp = sum(abs_fe),
# fetemp_grp = sum(abs_tempfe)) %>%
# ggplot(aes(x = fetemp_grp, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
# geom_point(size = 3, alpha = 0.5) +
# theme_bw() +
# ylab('') +
# xlab('Temperature-Iron-Related DE') +
# theme(axis.text.y = element_blank());p3_tempfe
#
#
# grid.arrange(blank_p, p1_fe, p2_temp, p3_tempfe, nrow = 1)
# DE plot with positive and negative differences shown.
pn_fe <- tfg_de_df %>%
group_by(grpnorm_taxgrp) %>%
summarise(fe_grp = sum(abs_fe),
fe_grp_neg = sum(fe_neg_de),
fe_grp_pos = sum(fe_pos_de)) %>%
ggplot(aes(x = fe_grp_neg, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
geom_point(size = 3, alpha = 0.5, colour = 'blue') +
geom_point(aes(x = fe_grp_pos, y = fct_reorder(grpnorm_taxgrp, fe_grp)),
size = 3, alpha = 0.5, colour = 'red') +
geom_segment(aes(x = fe_grp_neg, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'blue', alpha = 0.2, lwd = 2) +
geom_segment(aes(x = fe_grp_pos, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'red', alpha = 0.2, lwd = 2) +
theme_bw() +
xlab('Iron-Related DE') +
ylab('') +
theme(axis.text.y = element_blank());pn_fe
pn_temp <- tfg_de_df %>%
group_by(grpnorm_taxgrp) %>%
summarise(fe_grp = sum(abs_fe),
temp_grp_neg = sum(temp_neg_de),
temp_grp_pos = sum(temp_pos_de)) %>%
ggplot(aes(x = temp_grp_neg, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
geom_point(size = 3, alpha = 0.5, colour = 'blue') +
geom_point(aes(x = temp_grp_pos, y = fct_reorder(grpnorm_taxgrp, fe_grp)),
size = 3, alpha = 0.5, colour = 'red') +
geom_segment(aes(x = temp_grp_neg, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'blue', alpha = 0.2, lwd = 2) +
geom_segment(aes(x = temp_grp_pos, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'red', alpha = 0.2, lwd = 2) +
theme_bw() +
xlab('Temperature-Related DE') +
ylab('') +
theme(axis.text.y = element_blank());pn_temp
pn_tempfe <- tfg_de_df %>%
group_by(grpnorm_taxgrp) %>%
summarise(fe_grp = sum(abs_fe),
fetemp_grp_neg = sum(tempfe_neg_de),
fetemp_grp_pos = sum(tempfe_pos_de)) %>%
ggplot(aes(x = fetemp_grp_neg, y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
geom_point(size = 3, alpha = 0.5, colour = 'blue') +
geom_point(aes(x = fetemp_grp_pos, y = fct_reorder(grpnorm_taxgrp, fe_grp)),
size = 3, alpha = 0.5, colour = 'red') +
geom_segment(aes(x = fetemp_grp_neg, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'blue', alpha = 0.2, lwd = 2) +
geom_segment(aes(x = fetemp_grp_pos, xend = 0,
y = fct_reorder(grpnorm_taxgrp, fe_grp),
yend = fct_reorder(grpnorm_taxgrp, fe_grp)), colour = 'red', alpha = 0.2, lwd = 2) +
theme_bw() +
xlab('Iron-Temperature-Related DE') +
ylab('') +
theme(axis.text.y = element_blank());pn_tempfe
grid.arrange(blank_p, pn_fe, pn_temp, pn_tempfe, nrow = 1)
##`````````````````````````````````````````````````````````````````````````````````````````````````````````````````````````````````````##
##-------------------------------------------------------------------------------------------------------------------------------------##
#this does the same thing as above, but for MCL data
# Analysis of differential expression for temperature and Fe metatranscriptomics.
library(magrittr)
library(ggplot2)
library(beepr)
library(dplyr)
library(ggfortify)
library(testthat)
library(reshape2)
library(tidyverse)
library(edgeR)
library(gridExtra)
library(statmod)
# load group normalized data
#LJ can also do this for MCL data.. Import the MCL data, combine the cluster# and taxa to make clusters unique
#then change the name of the taxa.group column to grpnorm_taxgrp to fit in with the rest of this code.
grp_norm <- read.csv("annotation_allTFG.grpnorm_mmetsp_fc_pn_reclassified.summarygrouped_cluster.edgeR.csv")
grp_norm$orf_id <- paste (grp_norm$cluster, grp_norm$Taxa.group)
colnames(grp_norm)[1] <- "grpnorm_taxgrp"
grp_norm <- dplyr::filter (grp_norm, grepl('Pseudo-nit|Fragilariopsis',grpnorm_taxgrp))
#grp_norm <- read.csv("annotation_allTFG.grpnorm_mmetsp_fc_pn_reclassified.edgeR.csv")
# read in experiment key with associated treatments
tfg_key <- read.csv("tfg_key.csv")
tfg_key2 <- tfg_key %>%
dplyr::filter(time == 5 | time == 0,
b12 != 1 | is.na(b12))
# subset large original dataframe
grp_norm_sub <- grp_norm %>% dplyr::select('orf_id',# 'group',
'grpnorm_taxgrp', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C', 'TFG_t0_A',
'TFG_t0_B', 'TFG_t0_C')
grp_norm_sub_not0 <- grp_norm %>% dplyr::select('orf_id',# 'group',
'grpnorm_taxgrp', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C')
# change the row names to be the ORF ID
rownames(grp_norm_sub) <- grp_norm_sub$orf_id
# combine the expression values all into one column, with each referring to a sample ID
grp_norm_t <- melt(grp_norm_sub, variable.name = 'sample_key',
value.name = 'expression_value') %>%
inner_join(y = tfg_key, by = 'sample_key')
# read in normalization factors
norm_factors <- read.csv("norm_factors_mmetsp_fc_pn_reclassified.csv")
norm_factors_sub <- norm_factors %>% dplyr::select('group', 'TFG_t5_1A', 'TFG_t5_1B', 'TFG_t5_1C',
'TFG_t5_3A', 'TFG_t5_3B', 'TFG_t5_3C', 'TFG_t5_4A',
'TFG_t5_4B', 'TFG_t5_4C', 'TFG_t5_6A', 'TFG_t5_6B',
'TFG_t5_6C', 'TFG_t5_7A', 'TFG_t5_7B', 'TFG_t5_7C',
'TFG_t5_9A', 'TFG_t5_9B', 'TFG_t5_9C')
# making a dataframe of taxon specific normalization factors
tax_specific_abundance_norms <- data.frame(grpnorm_taxgrp = norm_factors$group,
norm_factors_group = rowMeans(norm_factors_sub[,c(2:ncol(norm_factors_sub))]))
# grouping of treatments
samples_present <- inner_join(x = data.frame(sample_key = names(grp_norm_sub_not0)[3:23]),
y = tfg_key, by = 'sample_key')
treatment_groups <- paste(samples_present$temp, samples_present$fe)
## multiplying abundance scaling factors
grp_norm_sub_not0 <- inner_join(x = grp_norm_sub_not0,
y = tax_specific_abundance_norms,
by = 'grpnorm_taxgrp')
grp_norm_sub_scaled <- grp_norm_sub_not0[c(3:20)]*grp_norm_sub_not0$norm_factors_group
# making a 'DGE List' for edgeR differential expression analysis
dge_list_tfg <- DGEList(counts = grp_norm_sub_scaled,
group = treatment_groups,
remove.zeros = FALSE,
genes = grp_norm_sub_not0$orf_id)
## used for old analysis with traditional model formulation
# fe <- as.logical(samples_present$fe)
# temperature_factor <- as.factor(temperature)
groups <- paste('fe', samples_present$fe, 'temp', samples_present$temp, sep = '_')
groups <- gsub(pattern = "-", replacement = "", x = groups)
# model matrix with each individual group as a unique factor
tfg_mm_factors <- model.matrix(~0 + groups)
# tfg_mm_contin is the old model formulation
# tfg_mm_contin <- model.matrix(~fe*temperature_factor)
# estimating dispersion parameters
tfg_disp_factors <- estimateGLMCommonDisp(dge_list_tfg,
design = tfg_mm_factors)
# tfg_disp_contin <- estimateGLMCommonDisp(dge_list_tfg,
# design = tfg_mm_contin)
# fitting gene-wise models
tfg_fit_factors <- glmQLFit(tfg_disp_factors, design = tfg_mm_factors, robust = TRUE)
# tfg_fit_contin <- glmQLFit(tfg_disp_contin, design = tfg_mm_contin, robust = TRUE)
# quasi likelihood DE test
# setting up contrasts to look at fe, temp, and interactions. See these links for guidance:
# for contrast formulation of temp_3vstemp_05:
# the first set of contrasts are pairwise contrasts.
my_contrasts <- makeContrasts(fe0_temp3vstemp05 = groupsfe_0_temp_3 - groupsfe_0_temp_0.5,
fe0_temp6vstemp05 = groupsfe_0_temp_6 - groupsfe_0_temp_0.5,
fe0_temp6vstemp3 = groupsfe_0_temp_6 - groupsfe_0_temp_3,
fe2_temp3vstemp05 = groupsfe_2_temp_3 - groupsfe_2_temp_0.5,
fe2_temp6vstemp05 = groupsfe_2_temp_6 - groupsfe_2_temp_0.5,
fe2_temp6vstemp3 = groupsfe_2_temp_6 - groupsfe_2_temp_3,
# Fe pairwise comparisons
temp05_fe2vsfe0 = groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5,
temp3_fe2vsfe0 = groupsfe_2_temp_3 - groupsfe_0_temp_3,
temp6_fe2vsfe0 = groupsfe_2_temp_6 - groupsfe_0_temp_6,
# fe_all contrast: all the coefficients associated with iron compared with those without iron. testing overall expression of +Fe treatments
fe_all = (groupsfe_2_temp_0.5 + groupsfe_2_temp_3 + groupsfe_2_temp_6 - groupsfe_0_temp_0.5 - groupsfe_0_temp_3 - groupsfe_0_temp_6)/3,
# testing overall expression of Temp 3 treatments compared with temp 0.5
temp_3vstemp_05 = ((groupsfe_2_temp_3 - groupsfe_2_temp_0.5) + (groupsfe_0_temp_3 - groupsfe_0_temp_0.5))/2,
# testing overall expression of Temp 6 treatments compared with temp 0.5
temp_6vstemp_05 = ((groupsfe_2_temp_6 - groupsfe_2_temp_0.5) + (groupsfe_0_temp_6 - groupsfe_0_temp_0.5))/2,
# testing overall expression fo Temp 6 treatments compared with temp 3
temp_6vstemp_3 = ((groupsfe_2_temp_6 - groupsfe_2_temp_3) + (groupsfe_0_temp_6 - groupsfe_0_temp_3))/2,
# testing interaction between temp and iron, between temps 6 and 0.5
tempfe_interaction_temp_6vstemp_05 = (groupsfe_2_temp_6 - groupsfe_0_temp_6) - (groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5),
# testing interaction between temp and iron, between temps 6 and 0.5
tempfe_interaction_temp_3vstemp_05 = (groupsfe_2_temp_3 - groupsfe_0_temp_3) - (groupsfe_2_temp_0.5 - groupsfe_0_temp_0.5),
levels = tfg_mm_factors)
# pairwise comparisons
# temperature pairwise comparisons
# low iron
fe0_temp3vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp3vstemp05'])
fe0_temp6vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp6vstemp05'])
fe0_temp6vstemp3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp6vstemp3'])
# high iron
fe2_temp3vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp3vstemp05'])
fe2_temp6vstemp05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp6vstemp05'])
fe2_temp6vstemp3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp6vstemp3'])
# fe pairwise comparisons
temp05_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp05_fe2vsfe0'])
temp3_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp3_fe2vsfe0'])
temp6_fe2vsfe0_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp6_fe2vsfe0'])
# overall Fe DE values testing
fe_all_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe_all'])
# temperature comparison values
temp_3vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_3vstemp_05'])
temp_6vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_6vstemp_05'])
temp_6vstemp_3_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'temp_6vstemp_3'])
#temperature and Fe 'interaction' values
tempfe_interaction_temp_6vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'tempfe_interaction_temp_6vstemp_05'])
tempfe_interaction_temp_3vstemp_05_test <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'tempfe_interaction_temp_3vstemp_05'])
# function for processing topTags() output that spits out the logFC and adjusted p value
out_toptag <- function(qlf_test_output){
# qlf_test_output <- fe_all_test
top_out <- topTags(qlf_test_output, n = Inf, adjust.method = 'BH', sort.by = 'none')
# get name of input
nm <- deparse(substitute(qlf_test_output))
nm_adj <- gsub(pattern = "_test", replacement = "", x = nm)
# making the foldchange and p value columns
foldchange <- top_out[[1]]$logFC
pvalue <- top_out[[1]]$FDR
result_df <- data.frame(foldchange, pvalue)
#adjusting names so that they have the test name appended with 'pvalue' and 'foldchange'
names(result_df) <- paste0(nm_adj, "_", names(result_df))
return(result_df)
}
## up / down / none decisions about DE genes
# pairwise comparisons
# temperature comparisons:
# low iron
fe0_temp3vstemp05_decide <- decideTestsDGE(fe0_temp3vstemp05_test)
fe0_temp3vstemp05_info <- out_toptag(fe0_temp3vstemp05_test)
fe0_temp6vstemp05_decide <- decideTestsDGE(fe0_temp6vstemp05_test)
fe0_temp6vstemp05_info <- out_toptag(fe0_temp6vstemp05_test)
fe0_temp6vstemp3_decide <- decideTestsDGE(fe0_temp6vstemp3_test)
fe0_temp6vstemp3_info <- out_toptag(fe0_temp6vstemp3_test)
# high iron
fe2_temp3vstemp05_decide <- decideTestsDGE(fe2_temp3vstemp05_test)
fe2_temp3vstemp05_info <- out_toptag(fe2_temp3vstemp05_test)
fe2_temp6vstemp05_decide <- decideTestsDGE(fe2_temp6vstemp05_test)
fe2_temp6vstemp05_info <- out_toptag(fe2_temp6vstemp05_test)
fe2_temp6vstemp3_decide <- decideTestsDGE(fe2_temp6vstemp3_test)
fe2_temp6vstemp3_info <- out_toptag(fe2_temp6vstemp3_test)
# fe pairwise comparisons
temp05_fe2vsfe0_decide <- decideTestsDGE(temp05_fe2vsfe0_test)
temp05_fe2vsfe0_info <- out_toptag(temp05_fe2vsfe0_test)
temp3_fe2vsfe0_decide <- decideTestsDGE(temp3_fe2vsfe0_test)
temp3_fe2vsfe0_info <- out_toptag(temp3_fe2vsfe0_test)
temp6_fe2vsfe0_decide <- decideTestsDGE(temp6_fe2vsfe0_test)
temp6_fe2vsfe0_info <- out_toptag(temp6_fe2vsfe0_test)
# Fe decision
fe_all_decide <- decideTestsDGE(fe_all_test)
fe_all_info <- out_toptag(fe_all_test)
# Temperature decision
temp_3vstemp_05_decide <- decideTestsDGE(temp_3vstemp_05_test)
temp_3vstemp_05_info <- out_toptag(temp_3vstemp_05_test)
temp_6vstemp_05_decide <- decideTestsDGE(temp_6vstemp_05_test)
temp_6vstemp_05_info <- out_toptag(temp_6vstemp_05_test)
temp_6vstemp_3_decide <- decideTestsDGE(temp_6vstemp_3_test)
temp_6vstemp_3_info <- out_toptag(temp_6vstemp_3_test)
# interaction DE decision
tempfe_interaction_temp_6vstemp_05_decide <- decideTestsDGE(tempfe_interaction_temp_6vstemp_05_test)
tempfe_interaction_temp_6vstemp_05_info <- out_toptag(tempfe_interaction_temp_6vstemp_05_test)
tempfe_interaction_temp_3vstemp_05_decide <- decideTestsDGE(tempfe_interaction_temp_3vstemp_05_test)
tempfe_interaction_temp_3vstemp_05_info <- out_toptag(tempfe_interaction_temp_3vstemp_05_test)
# checking total number of DE genes for each test
# [email protected] %>% abs() %>% sum()
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# getting only the rows which do not have na for grpnorm_taxgrp
#grp_norm_no_grp_na <- grp_norm[!is.na(grp_norm$grpnorm_taxgrp),]
#LJ changed the line above into this because I didn't have any NA values
grp_norm_no_grp_na <- dplyr::filter (grp_norm, !grepl('^$', grpnorm_taxgrp))
# dataframe with actual values used for DE analysis (transformed vals by tax-specific scaling factor)
grp_norm_sub_scaled_copy <- grp_norm_sub_scaled
names(grp_norm_sub_scaled_copy) <- paste0(names(grp_norm_sub_scaled_copy), '-scaled')
## making compiled dataframe
tfg_de_df <- data.frame(Fe_vs_noFe_de = fe_all_decide %>% as.vector(),
Fe_vs_noFe_pvalue = fe_all_info$fe_all_pvalue,
Fe_vs_noFe_foldchange = fe_all_info$fe_all_foldchange,
# temperature comparisons
temp_3C_vs_0C_de = temp_3vstemp_05_decide %>% as.vector(),
temp_3C_vs_0C_pvalue = temp_3vstemp_05_info$temp_3vstemp_05_pvalue,
temp_3C_vs_0C_foldchange = temp_3vstemp_05_info$temp_3vstemp_05_foldchange,
temp_6C_vs_0C_de = temp_6vstemp_05_decide %>% as.vector(),
temp_6C_vs_0C_pvalue = temp_6vstemp_05_info$temp_6vstemp_05_pvalue,
temp_6C_vs_0C_foldchange = temp_6vstemp_05_info$temp_6vstemp_05_foldchange,
temp_6C_vs_3C_de = temp_6vstemp_3_decide %>% as.vector(),
temp_6C_vs_3C_pvalue = temp_6vstemp_3_info$temp_6vstemp_3_pvalue,
temp_6C_vs_3C_foldchange = temp_6vstemp_3_info$temp_6vstemp_3_foldchange,
int_fe_temp_6C_vs_0C_de = tempfe_interaction_temp_6vstemp_05_decide %>% as.vector(),
int_fe_temp_6C_vs_0C_pvalue = tempfe_interaction_temp_6vstemp_05_info$tempfe_interaction_temp_6vstemp_05_pvalue,
int_fe_temp_6C_vs_0C_foldchange = tempfe_interaction_temp_6vstemp_05_info$tempfe_interaction_temp_6vstemp_05_foldchange,
int_fe_temp_3C_vs_0C_de = tempfe_interaction_temp_3vstemp_05_decide %>% as.vector(),
int_fe_temp_3C_vs_0C_pvalue = tempfe_interaction_temp_3vstemp_05_info$tempfe_interaction_temp_3vstemp_05_pvalue,
int_fe_temp_3C_vs_0C_foldchange = tempfe_interaction_temp_3vstemp_05_info$tempfe_interaction_temp_3vstemp_05_foldchange,
# pairwise comparisons
noFe_3C_vs_noFe_0C_de = fe0_temp3vstemp05_decide %>% as.vector(),
noFe_3C_vs_noFe_0C_pvalue = fe0_temp3vstemp05_info$fe0_temp3vstemp05_pvalue,
noFe_3C_vs_noFe_0C_foldchange = fe0_temp3vstemp05_info$fe0_temp3vstemp05_foldchange,
Fe_3C_vs_Fe_0C_de = fe2_temp3vstemp05_decide %>% as.vector(),
Fe_3C_vs_Fe_0C_pvalue = fe2_temp3vstemp05_info$fe2_temp3vstemp05_pvalue,
Fe_3C_vs_Fe_0C_foldchange = fe2_temp3vstemp05_info$fe2_temp3vstemp05_foldchange,
noFe_6C_vs_noFe_0C_de = fe0_temp6vstemp05_decide %>% as.vector(),
noFe_6C_vs_noFe_0C_pvalue = fe0_temp6vstemp05_info$fe0_temp6vstemp05_pvalue,
noFe_6C_vs_noFe_0C_foldchange = fe0_temp6vstemp05_info$fe0_temp6vstemp05_foldchange,
Fe_6C_vs_Fe_0C_de = fe2_temp6vstemp05_decide %>% as.vector(),
Fe_6C_vs_Fe_0C_pvalue = fe2_temp6vstemp05_info$fe2_temp6vstemp05_pvalue,
Fe_6C_vs_Fe_0C_foldchange = fe2_temp6vstemp05_info$fe2_temp6vstemp05_foldchange,
noFe_6C_vs_noFe_3C_de = fe0_temp6vstemp3_decide %>% as.vector(),
noFe_6C_vs_noFe_3C_pvalue = fe0_temp6vstemp3_info$fe0_temp6vstemp3_pvalue,
noFe_6C_vs_noFe_3C_foldchange = fe0_temp6vstemp3_info$fe0_temp6vstemp3_foldchange,
Fe_6C_vs_Fe_3C_de = fe2_temp6vstemp3_decide %>% as.vector(),
Fe_6C_vs_Fe_3C_pvalue = fe2_temp6vstemp3_info$fe2_temp6vstemp3_pvalue,
Fe_6C_vs_Fe_3C_foldchange = fe2_temp6vstemp3_info$fe2_temp6vstemp3_foldchange,
Fe_0C_vs_noFe_0C_de = temp05_fe2vsfe0_decide %>% as.vector(),
Fe_0C_vs_noFe_0C_pvalue = temp05_fe2vsfe0_info$temp05_fe2vsfe0_pvalue,
Fe_0C_vs_noFe_0C_foldchange = temp05_fe2vsfe0_info$temp05_fe2vsfe0_foldchange,
Fe_3C_vs_noFe_3C_de = temp3_fe2vsfe0_decide %>% as.vector(),
Fe_3C_vs_noFe_3C_pvalue = temp3_fe2vsfe0_info$temp3_fe2vsfe0_pvalue,
Fe_3C_vs_noFe_3C_foldchange = temp3_fe2vsfe0_info$temp3_fe2vsfe0_foldchange,
Fe_6C_vs_noFe_6C_de = temp6_fe2vsfe0_decide %>% as.vector(),
Fe_6C_vs_noFe_6C_pvalue = temp6_fe2vsfe0_info$temp6_fe2vsfe0_pvalue,
Fe_6C_vs_noFe_6C_foldchange = temp6_fe2vsfe0_info$temp6_fe2vsfe0_foldchange,
# including dataframe with annotations
grp_norm_no_grp_na,
# including scaled values,
grp_norm_sub_scaled_copy,
# columns for plotting DE analysis
fe_neg_de = ifelse(fe_all_decide == -1, yes = -1, no = 0) %>% as.vector(),
fe_pos_de = ifelse(fe_all_decide == 1, yes = 1, no = 0) %>% as.vector(),
# temperature is a bit harder than Fe. The gene has to be DE in either comparisons from 3vs0.5 *or* 6vs0.5 to be counted in this column. But if the gene is negatively expressed from 3vs0.5, and positively expressed from 6vs0.5, it would be excluded.
temp_neg_de = ifelse((temp_3vstemp_05_decide == -1 | temp_6vstemp_05_decide == -1) &
(temp_3vstemp_05_decide != 1 | temp_6vstemp_05_decide != 1),
yes = -1, no = 0) %>% as.vector(),
temp_pos_de = ifelse((temp_3vstemp_05_decide == 1 | temp_6vstemp_05_decide == 1) &
(temp_3vstemp_05_decide != -1 | temp_6vstemp_05_decide != -1),
yes = 1, no = 0) %>% as.vector(),
tempfe_neg_de = ifelse((tempfe_interaction_temp_6vstemp_05_decide == -1 | tempfe_interaction_temp_3vstemp_05_decide == -1) &
(tempfe_interaction_temp_6vstemp_05_decide != 1 & tempfe_interaction_temp_3vstemp_05_decide != 1),
yes = -1, no = 0) %>% as.vector(),
tempfe_pos_de = ifelse((tempfe_interaction_temp_6vstemp_05_decide == 1 | tempfe_interaction_temp_3vstemp_05_decide == 1) &
(tempfe_interaction_temp_6vstemp_05_decide != -1 & tempfe_interaction_temp_3vstemp_05_decide != -1),
yes = 1, no = 0) %>% as.vector(),
# abs_fe is for ranking taxonomic groups for plotting later on.
abs_fe = ifelse(abs(fe_all_decide) == 1, yes = 1, no = 0) %>% as.vector())
# old analysis
# fe0_temp05vs3 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp05vstemp3'])
# fe0_temp05vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp05vstemp6'])
# fe0_temp3vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe0_temp3vstemp6'])
#
# fe2_temp05vs3 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp05vstemp3'])
# fe2_temp05vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp05vstemp6'])
# fe2_temp3vs6 <- glmQLFTest(tfg_fit_factors, contrast = my_contrasts[,'fe2_temp3vstemp6'])
#
#
# fe0_temp05vs3_decide <- decideTestsDGE(object = fe0_temp05vs3)
# fe0_temp05vs6_decide <- decideTestsDGE(object = fe0_temp05vs6)
# fe0_temp3vs6_decide <- decideTestsDGE(object = fe0_temp3vs6)
#
# fe2_temp05vs3_decide <- decideTestsDGE(object = fe2_temp05vs3)
# fe2_temp05vs6_decide <- decideTestsDGE(object = fe2_temp05vs6)
# fe2_temp3vs6_decide <- decideTestsDGE(object = fe2_temp3vs6)
#
#
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
# [email protected] %>% abs() %>% sum()
## getting significance tests of old model formulation
tfg_inter <- glmQLFTest(tfg_fit_contin, coef = 1)
tfg_fe <- glmQLFTest(tfg_fit_contin, coef = 2)
tfg_temp3 <- glmQLFTest(tfg_fit_contin, coef = 3)
tfg_temp6 <- glmQLFTest(tfg_fit_contin, coef = 4)
tfg_fetemp3 <- glmQLFTest(tfg_fit_contin, coef = 5)
tfg_fetemp6 <- glmQLFTest(tfg_fit_contin, coef = 6)
#
# tfg_inter_decide <- decideTestsDGE(tfg_inter)
# tfg_fe_decide <- decideTestsDGE(tfg_fe)
# tfg_temp3_decide <- decideTestsDGE(tfg_temp3)
# tfg_temp6_decide <- decideTestsDGE(tfg_temp6)
# tfg_fetemp3_decide <- decideTestsDGE(tfg_fetemp3)
# tfg_fetemp6_decide <- decideTestsDGE(tfg_fetemp6)
### old version writing final dataframe
# tfg_de_df <- data.frame(tfg_inter_decide, tfg_fe_decide, tfg_temp3_decide,
# tfg_temp6_decide, tfg_fetemp3_decide, tfg_fetemp6_decide,
# grp_norm_sub_not0,
# abs_fe = ifelse(abs(tfg_fe_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# abs_temp = ifelse(abs(tfg_temp3_decide) == 1 | abs(tfg_temp6_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# abs_tempfe = ifelse(abs(tfg_fetemp3_decide) == 1 | abs(tfg_fetemp6_decide) == 1, yes = 1, no = 0) %>% as.vector(),
# # summaries of negative DE by treatment *group*
# fe_neg_de = ifelse((tfg_fe_decide == -1 | tfg_fe_decide == -1) &
# (tfg_fe_decide != 1 | tfg_fe_decide!= 1), yes = -1, no = 0) %>% as.vector(),
# temp_neg_de = ifelse((tfg_temp3_decide == -1 | tfg_temp6_decide == -1) &
# (tfg_temp3_decide != 1 | tfg_temp6_decide!= 1), yes = -1, no = 0) %>% as.vector(),
# fetemp_neg_de = ifelse((tfg_fetemp3_decide == -1 | tfg_fetemp6_decide == -1) &
# (tfg_fetemp3_decide != 1 | tfg_fetemp6_decide!= 1), yes = -1, no = 0) %>% as.vector(),
#
# # summaries of positive DE by treatment *group*
# fe_pos_de = ifelse((tfg_fe_decide == 1 | tfg_fe_decide == 1) &
# (tfg_fe_decide != -1 | tfg_fe_decide!= -1), yes = 1, no = 0) %>% as.vector(),
# temp_pos_de = ifelse((tfg_temp3_decide == 1 | tfg_temp6_decide == 1) &
# (tfg_temp3_decide != -1 | tfg_temp6_decide!= -1), yes = 1, no = 0) %>% as.vector(),
# fetemp_pos_de = ifelse((tfg_fetemp3_decide == 1 | tfg_fetemp6_decide == 1) &
# (tfg_fetemp3_decide != -1 | tfg_fetemp6_decide!= -1), yes = 1, no = 0) %>% as.vector())
write.csv(tfg_de_df, file = "MCL_tfg_de_annotation_frag-pseudo_allTFG_grpnorm_mmetsp_fc_pn_reclassified.csv")
### plotting de results by taxon
# blank plot just used for the axis.
blank_p <- tfg_de_df %>%
group_by(grpnorm_taxgrp) %>%
summarise(fe_grp = sum(abs_fe)) %>%
ggplot(aes(x = fe_grp,
y = fct_reorder(grpnorm_taxgrp, fe_grp))) +
# geom_point() +
theme_bw() +