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# On-Demand Seizures Facilitate Rapid Screening of Therapeutics for Epilepsy # Authors: Yuzhang Chen, Brian Litt, Flavia Vitale, Hajime Takano # DOI: https://doi.org/10.7554/eLife.101859 # Step 1: Import Libraries and Master Spreadsheet library(readxl) library(ggplot2) library(ggbreak) library(ggpubr) library(tidyver...
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################### ################### ################### ################### ################### ################### #Run this script for sensitivity analyses to reproduce Section S3.1 (Pre-Injury Psychiatric Vulnerability) ################### ################### ################### ################### #############...
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--- title: "Analysis MMRs Maturation - No posthoc" output: html_document: default pdf_document: default date: '2023-12-11' --- ## 1. Preparing the data for the analysis First, we load some packages. ```{r} #install.packages("foreign") #install.packages("dyplr") #install.packages("tidyr") #instal...
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#' return msdap package version as a string #' #' simple wrapper around utils::packageVersion() #' @export msdap_version = function() { as.character(packageVersion("msdap")) } #' get a value set using options(), throwing error for invalid type (boolean) #' #' @param x option name for `getOption()` #' @export get_...
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# Load packages ----------------------------------- rm(list = ls()) library(here) library(tidyr) library(dplyr) library(readr) library(glue) library(tibble) library(ggplot2) library(cowplot) library(tidyverse) library(readxl) library(RColorBrewer) library(ggpubr) # Organize environment ------------------------------...
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#' generate color-coding for all sample metadata #' @param samples sample metadata table, typically; dataset$samples #' @importFrom gtools mixedsort #' @importFrom ggplot2 cut_interval #' @importFrom colorspace sequential_hcl sample_color_coding = function(samples) { color_categorical = list( # https://observabl...
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# ============================================================= # ASSOCIATIONS OF INDIVIDUAL AGEING BIOMARKERS WITH ALL-CAUSE MORTALITY # ============================================================= # COHORT: # Lothian Birth Cohort 1936 # COX MODELS: # Models are fitted separately for each ageing biomarker. # # ...
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--- title: "Mouse_SOX2-_SOX10+_subclustering_and_annotation" output: html_document date: "2025-04-17" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) l...
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--- title: "Mouse_clustering_and_annotation" output: html_document date: "2025-04-16" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(tidyverse) library(harmony) library(patchwork) library(scales) library(scCustomi...
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library(ggplot2) ## Make a bar graph to summarize proportion of clusters/programs/etc in each sample ## @para: x, x-axis data ## @para: y, y-axis data ## @para: x_order: order of x-axis variables ## @para: y_order: order of y-axis variables ## @para: col_names: column names for df for plotting ## @para: x_var: name of...
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--- title: "Cleaning LL14" output: html_document date: "2023-12-06" --- ```{r setup, include=FALSE} knitr::opts_chunk$set( echo = FALSE, # don't print the code chunk warning = FALSE, # don't print warnings message = FALSE, # don't print messages fig.width = 8, # set default width of figures fig.height = ...
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--- title: "Elevated Hippocampal Activity at Turnaround" output: html_document date: "2024-03-26" --- ```{r setup, include=FALSE} ## libraries ## library(tidyverse) library(ggplot2) library(lmerTest) library(doParallel) library(parallel) library(foreach) library(here) library(fs) library(lmtest) library(brms) library(...
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#' Compare the number of peptide detection counts between groups #' #' The computation of scores is detailed in the online vignitte for "differential testing". #' #' @param dataset a valid dataset #' @param min_peptides_observed minimum number of peptides for a protein to pass filtering rules (i.e. otherwise, no z-sco...
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--- title: "Pseudo DEG co-culture vs no mono-culture EP1NS" author: "Sara Danielli" date: '`r format(Sys.time(), "Last modified: %b %d %Y")`' output: html_document: toc: yes df_print: paged --- ## Set up ```{r, setup, include = FALSE} # Load packages ----------------------------------- library(knitr) opts_ch...
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--- output: rmarkdown::github_document: html_preview: true toc: true --- ```{r, include = FALSE} knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) ``` This vignette details the main functions of the MS-DAP R package. If you have not installed MS-DAP yet, check out the installation guides and ex...
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#' placeholder title #' @param tib_input todo #' @param samples todo #' @param isdia todo plot_abundance_distributions = function(tib_input, samples, isdia) { param_density_bandwidth = "sj" param_density_adjust = 1.0 # alternatively, 0.9 # for DIA datasets, only use abundances for peptides detected at some q-va...
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#' Create gene-level summary tables for your DEA and differential detection results #' #' @description #' #' To expedite downstream analysis, this function maps the proteingroup results from your #' differential expression analysis to Human gene identifiers and exports these as Excel tables that are ready for #' use w...
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library(biomaRt) library(Seurat) library(tidyverse) library(qs) library(glue) library(data.table) library(infercnv) library(matrixStats) source('~/Projects/General-Codes/Resources/Plotting_helper_functions.R') source('~/Projects/General-Codes/Resources/single_cell_preprocessing_helper_functions.R') source('~/Projects/...
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prep_conn_plot_df <- function(df, sub){ # filter to subject # conn_sub_df <- df %>% rename(pval = percent_sig) %>% filter(subject == sub) %>% arrange(pairs) # correct for time points # conn_sub_sig_df <- conn_sub_df %>% mutate(roi_pair = paste0(first_region, "_", second_region)) %>% g...
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library(Seurat) library(ggplot2) library(patchwork) library(dplyr) library(DropletUtils) library(tidyverse) library(harmony) s1_filter_matrix <- Read10X("./s1_filter_mx/") s2_filter_matrix <- Read10X("./s2_filter_mx/") write10xCounts("./s1_filter_mx/filtered_feature_bc_matrix.h5", s1_filter_matrix, type = "HDF5", ...
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--- title: "Clinical Anxiety EDA" output: html_document date: "2024-01-17" --- ```{r setup, include=FALSE} knitr::opts_chunk$set( echo <- FALSE, # don't print the code chunk warning <- FALSE, # don't print warnings message <- FALSE, # don't print messages fig.width <- 5, # set default width of figures fi...
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adjust_flip_data <- function(df){ # Function: adjust_flip_data # Purpose: Prepares and cleans data for analysis by adjusting trial data based on flip events. # Input: # - df: A dataframe containing trial data, which includes variables like Trial, GhostLocation, trial_flip, etc. # Process: # - Filters ou...
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#for NGN2-neurons #Pipeline initally written by Alexander J Trostle #code to define disease signature, bin the resuce percentage, visualization for disease gene rescue rm(list = ls()) options(java.parameters = "-Xmx8g" ) setwd("path_to_wd") library(ggplot2) library(ggrepel) library(readxl) library(fgsea) library(pheat...
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library(dada2) library(dplyr) path <- "C:/Users/Jacobs Laboratory/Documents/JCYang/Raw_Data_March2022SeqRun/PFF_FastQ_Files/" # CHANGE to the directory containing the fastq files list.files(path) # Extract sample names, identify forward and reverse reads fnFs <- sort(list.files(path, pattern="R1", full.names = TRUE)...
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library(dada2) library(here) library(tidyverse) getwd() here::i_am("../pdbehavior/ASO_DADA2.R") path <- "/home/julianne/Documents/pd_paper/raw_data/" # CHANGE to the directory containing the fastq files list.files(path) # Extract sample names, identify forward and reverse reads fnFs <- sort(list.files(path, pattern="...
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--- title: "Progenitors_subclustering_and_annotation" output: html_document date: "2025-04-14" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(...
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# estimateParam --------------------------------------------------------- #' @name estimateParam #' @aliases estimateParam #' @title Estimate simulation parameters #' @description This function estimates and returns parameters needed for power simulations.\cr #' The user needs to choose the following options at least...
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library(scToppR) library(Seurat) library(tidyverse) library(harmony) library(patchwork) library(openxlsx) library(orthogene) # Mouse ectoderm and mesenchyme subclustering #subset E11 matching TW E11 data setwd("/scr1/users/manchela/Data") cds <- readRDS("face_mouse_final.rds") Idents(cds) <- "stage" E11 <- subset(cds...
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setwd('~/path to your ABCD 5.0 csv folder') ## Setting up environment library(psych) library(dplyr) library(purrr) library(tidyr) library(stringr) library(tableone) library(MatchIt) library(car) library(ggplot2) library(ggstatsplot) library(jtools) library(sensemakr) library(reshape2) library(emmeans) library(devtoo...
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#~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ #~~~~~~~~~~~~~~~~~~ FUNCTIONS MOSTLY RELEVANT TO ASSIGN PROGRAMS STEP~~~~~~~~~~~~~~~~~~~ #~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ # ReadMarkerGenes function takes in the location of ...
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# Utility ----------------------------------------------------------------- data_clean_rdk <- function(x){ if('Participant Public ID' %in% colnames(x)){ y <- x %>% as.data.frame() %>% rename(ID = `Participant Public ID`, Trial = `Trial number`, RT = `Total time for referenc...
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# ------------- Figure S3 -------------- #----Figure S3A---- #infercnv,Identify CNV levels at the gene level in epithelial cells #Extract epithelial cells corresponding to module patients rm(list = ls()) setwd("./t100553/wss") sce <- readRDS("./sce_Annotated_umap.rds") corrsce <- readRDS("./subsce.corr.rds") ep...
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--- output: rmarkdown::github_document: html_preview: true toc: true --- ```{r, include = FALSE} knitr::opts_chunk$set( collapse = TRUE, fig.path = "images/intro-", comment = "#>" ) ``` This document provides an introduction to MS-DAP; what is it and how does it work, together with highlights from th...
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#' returns all DEA functions integrated with MS-DAP #' #' @description #' #' ## available DEA functions #' **ebayes**: wrapper for the eBayes function from the limma package (PMID:25605792) <https://bioconductor.org/packages/release/bioc/html/limma.html>. The eBayes function applies moderated t-statistics to each row ...
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# ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ # This script is to fit a GLMM using INLA framework for the manuscript in PLOS ONE: # "Growth rates on coral reefs peaked at 25 °C through the Holocene" # by Tonya Macedo and Robert van Woesik # ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~...
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--- title: "ST-EPN malignant cells - sc/snRNA-seq (Figure 2)" author: "Sara Danielli" output: html_document: toc: yes df_print: paged --- ```{r, setup, include = FALSE} library(knitr) opts_chunk$set( echo = TRUE, cache = TRUE, warning = FALSE, comment = FALSE) ``` ```{r preparation environment, message=FA...
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##' The leverages of PCA model indicate how much influence each ##' observation has on the PCA model. Observations with high leverage ##' has caused the principal components to rotate towards them. It can ##' be used to extract both "unimportant" observations as well as ##' picking potential outliers. ##' ##' Defined a...
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library(infercnv) addNormalControl <- function(ext_ctrl, inferCNV_analysis_folder, cm_raw, orig_samples, type){ ## Read ctrl cm message("Loading normal control count matrix...") if (type == 'frozen'){ suffix <- "_nuc_premrna_counts.rds" } else if (type == 'fresh') { suffix <- "_fresh_counts.rds" } ...
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# readall8.r Plot power spectra for classes. # Normalize: # Divide power by power in target-aligned interval prior to time 0 # Now values are expressed as percentage of baseline # Specific for each site and for each frequency # (stack & class are not relevant to baseline) # # Scale: # Give all sites equal weight, AF...
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#' Perform differential neighbourhood abundance testing #' #' This will perform differential neighbourhood abundance testing after cell #' counting. #' @param x A \code{\linkS4class{Milo}} object with a non-empty #' \code{nhoodCounts} slot. #' @param design A \code{formula} or \code{model.matrix} object describing the ...
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#' Import a label-free proteomics dataset from FragPipe; combines quantitative data from the MSstats.csv file with PSM data from psm.tsv files #' #' @description #' This function requires the following FragPipe output data: #' #' - 'combined_protein.tsv' file, located in the FragPipe output folder #' - 'MSstats.csv' f...
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#' placeholder title #' @param peptides todo #' @param samples todo #' @param isdia todo #' @importFrom data.table setorder #' @importFrom patchwork wrap_plots plot_retention_time_v2 = function(peptides, samples, isdia) { param_density_bandwidth = "sj" param_density_adjust = 1.0 # alternatively, 0.9 # TODO: inpu...
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################### ################### ################### ################### #Bootstrapping (will run for ~40 minutes) ################### ################### ################### ################### set.seed(123) n <- length(sample_newTBI[,1]) B <- 1000 boot.samples <- matrix(sample(sample_newTBI$subclass, size=B*n...
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# remove scientific notation ---------------------------------------------- .plain <- function(x,...) { format(x, ..., scientific = FALSE, trim = TRUE, digits=1) } # ggplot colors ----------------------------------------------------------- #' @importFrom grDevices hcl .gg_color_hue <- function(n) { hues = seq(15...
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cli::cli_h2("┗ [Vasc-AoP] Loading visualizations") #--------------------# ####🔺Correlation #### #--------------------# corr_matrix_plot <- function(dat, vars, title = "") { return( dat |> dplyr::mutate( dplyr::across(where(is.character), factor), dpl...
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# ------------- Figure 5 -------------- #----Figure 5A---- library(Seurat) library(dplyr) library(tibble) library(pheatmap) library(tidyr) library(viper) library(decoupleR) library(ggplot2) library(patchwork) library(OmnipathR) # Infer transcription factor activity in CM2 and CM5 cells module2 <- readRDS("...
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#' placeholder title #' @param peptides todo #' @param prop_peptide todo peptides_collapse_by_sequence = function(peptides, prop_peptide = "sequence_plain") { tib_result = tibble_peptides_reorder(as_tibble(aggregate_tibble_by_datatables(peptides, prop_peptide))) return(tib_result) } #' Completely remove protein...
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#' Perform differential abundance testing using a NB-generalised linear mixed model #' #' This function will perform DA testing per-nhood using a negative binomial generalised linear mixed model #' @param X A matrix containing the fixed effects of the model. #' @param Z A matrix containing the random effects of the mod...
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--- title: "powsimR" output: rmdformats::material: highlight: kate self_contained: true code_folding: show thumbnails: true gallery: true fig_width: 8 fig_height: 4 df_print: kable fig_caption: yes use_bookdown: true bibliography: Bioc.bib link-citations: yes vignette: > %\Vi...
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# ------------- Figure 4 -------------- #----Figure 4A---- #Create CellChat objects for module2 and module5 library(CellChat) library(patchwork) library(tidyverse) options(stringsAsFactors = FALSE) corsce <- readRDS("./wss/subsce.corr.rds") corsce@meta.data <- corsce@meta.data[,c(4,5,25,24,27)] cancer.epi <- readRDS(fi...
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# simulateDE -------------------------------------------------------------- #' @name simulateDE #' @aliases simulateDE #' @title Simulate Differential Expression Pipeline #' @description simulateDE is the main function to simulate differential expression for RNA-seq experiments. #' The simulation parameters are speci...
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########################### ### MILO PLOTTING UTILS ### ########################### #' Plot histogram of neighbourhood sizes #' #' This function plots the histogram of the number of cells belonging to #' each neighbourhood #' #' @param milo A \code{\linkS4class{Milo}} object with a non-empty \code{nhoods} #' slot. #'...
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--- title: "Normative Gameplay on the Pacman Task from Pilot Data" output: html_document --- ```{r setup, include=FALSE} knitr::opts_chunk$set( echo <- FALSE, # don't print the code chunk warning <- FALSE, # don't print warnings message <- FALSE, # don't print messages fig.width <- 5, # set default width ...
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--- title: "granger_thresholds" output: html_document date: "2025-07-03" --- ```{r setup, include=FALSE} ## libraries ## library(tidyverse) library(ggplot2) library(lmerTest) library(doParallel) library(parallel) library(foreach) library(here) library(fs) library(lmtest) library(scales) library(ggthemr) library(RColorB...
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# checkup ----------------------------------------------------------------- #' @importFrom SingleCellExperiment SingleCellExperiment #' @importFrom scater isOutlier #' @importFrom BiocGenerics counts .run.checkup <- function(countData, readData, batchData, ...
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--- title: "hNPC_scRNAseq_analysis" author: "SabaShahin" date: "06/06/2023" output: html_document editor_options: chunk_output_type: console --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) ``` load required libraries ```{r} suppressWarnings(library(dplyr)) suppressWarnings(library(Seurat))...
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--- title: "Supercluster Statistics" output: html_notebook --- Version 1.0, July 2025, SA This script calculates a weighted average of data clustered together 100% consistently across leave1out iterations, and runs the statistical comparisons for each supercluster. It plots the supercluster connectivity profiles in...
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# Normalisation Wrapper --------------------------------------------------- .norm.calc <- function(Normalisation, sf, countData, spikeData, spikeInfo, batchData, Lengths, ...
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library(ggplot2) library(dplyr) library(magrittr) library(Seurat) library(scCustomize) library(tidyverse) library(harmony) mouse_cds1 <- readRDS("cds_face_mouse.rds") mouse_cds2 <- mouse_cds1 mouse_cds_ect <- readRDS("ect_all.rds") mouse_cds_mes <- readRDS("mes_all.rds") Idents(mouse_cds1) <- "cell_type1" mouse_cds_cn...
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R
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#' Input validation for eBayes/DEqMS/MS-EmpiRe functions #' #' @param eset protein/peptide log2 intensity matrix stored as a Biobase ExpressionSet. Must describe protein_id and sample_id in metadata #' @param model_matrix a `stats::model.matrix()` result that is supplied to `limma::lmFit()` #' @param model_matrix_res...
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R
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#neurogenomicslab/magma.celltyping Sys.setenv(GITHUB_PAT="your token") install.packages("piggyback") Sys.setenv('R_MAX_VSIZE'=64000000000) if(!require("remotes")) install.packages("remotes") library(MAGMA.Celltyping) library(qqman) face_ctd <- EWCE::load_rdata("ctd_face_ctd.rda") face_subtype_ctd <- EWCE::load_rdata...
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--- title: "Spatial_Expression" output: html_document date: "2025-04-07" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(patchwork) library(vir...
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local({ # the requested version of renv version <- "1.1.8" attr(version, "md5") <- "cbffd086c66739a0fdaac7a30b4aa65c" attr(version, "sha") <- NULL # the project directory project <- Sys.getenv("RENV_PROJECT") if (!nzchar(project)) { project <- getwd() } # use start-up diagn...
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R
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#' Import a label-free proteomics dataset from Bruker proteoscape #' #' This function was tested with a Proteoscape that uses DIA-NN 1.7.1, and expects the #' respective peptide.parquet and protein.parquet files with peptide and protein data. #' #' You can also import the report.tsv file generated by Proteoscape using...
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R
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#' plot peptide-level data #' #' @examples \dontrun{ #' # example 1: #' # <assuming you imported a dataset and applied analysis_quickstart()> #' # plot all significant proteins found by DEA #' plot_peptide_data( dataset, select_dea_signif = TRUE, #' # should match analysis_quickstart() parameters ! #' norm_algorit...
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# ------------- Figure 2 -------------- #----Figure 2A---- #co-occurrence analyses library(Seurat) library(dplyr) library(ggplot2) library(tidyverse) setwd("./NSCLC/Figure/figure2/") rm(list = ls()) TIME <- readRDS(file = "./NSCLC/Figure/figure1/TIME.rds") sce <- TIME #remove cell populations with low cell counts, low ...
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library(phyloseq) library(ggplot2) library(tibble) library(tidyr) library(tidyverse) library(plyr) library(dplyr) library(vegan) library(treeio) library(ape) library(pairwiseAdonis) ############################### #Script template for DADA2 ITS2 workflow ############################### #library(readr) #library(dada2)...
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R
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--- title: "NMF for ST-EPN" author: Sara Danielli date: '`r format(Sys.time(), "Last modified: %b %d %Y")`' output: rmdformats::readthedown: lightbox: true highlight: tango editor_options: chunk_output_type: console --- ```{r include = FALSE} library(knitr) opts_chunk$set(comment = NA, eval = FALSE) ``` ...
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R
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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R
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--- title: "MS-DAP: Mass Spectrometry Downstream Analysis Pipeline" subtitle: "version: `r msdap::msdap_version()` &nbsp; &nbsp; https://github.com/ftwkoopmans/msdap/" output: pdf_document: toc: true toc_depth: 2 number_sections: true latex_engine: xelatex keep_tex: false fontsize: 11pt geometry:...
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R
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library(EWCE) library(SingleCellExperiment) library(scRNAseq) library(scater) library(Seurat) library(tidyr) library(pheatmap) # Sys.setenv('R_MAX_VSIZE'=64000000000) options(future.globals.maxSize = 10 * 1024^3) setwd("/scr1/users/manchela/Data") cds_subtype <- readRDS("/scr1/users/manchela/Data/human_face_no-neuro_c...
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R
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##################################################################################################################### # ##################################################################################################################### # STEP 1 - NEURONS LVL2 DEVELOPMENT SUBSET CONTROL CELLS - CONTRASTS setwd("/datos...
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R
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#' check if peptide tibble has cache #' @param dataset your dataset #' @export check_dataset_hascache = function(dataset) { is.list(dataset) && all(c("groups","dt_pep_group") %in% names(dataset)) } #' invalidate peptide tibble cache #' @param dataset your dataset #' @export invalidate_cache = function(dataset) { ...
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R
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################### ################### ################### ################### #Summary Scores: Means and 95% Confidence Intervals across Iterations ################### ################### ################### ################### df_groupcomp <- data.frame(groupcomp.mtrx) summary_groupcomp <- data.frame( Comparison ...
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R
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#' Import sample metadata from an Excel table #' #' @param dataset your dataset #' @param filename full file path of the input file (eg; C:/temp/template_experiment1.xlsx) #' #' @export import_sample_metadata = function(dataset, filename) { # TODO: input validation stopifnot(is.list(dataset) && "peptides" %in% nam...
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R
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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R
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library(tximeta) library(DESeq2) library(tidyverse) library(readr) library(apeglm) library(ashr) library (EnhancedVolcano) library(gprofiler2) library(dplyr) library(IHW) library("variancePartition") library(edgeR) library(tximport) library(patchwork) library(cowplot) ##################################################...
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R
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--- title: "R Notebook" output: html_notebook --- ```{r } library(Seurat) library(Matrix) library(data.table) library(ggplot2) library(gridExtra) library(SeuratDisk) library(zellkonverter) library(ShinyCell) library(dplyr) library(clusterProfiler) library(org.Hs.eg.db) setwd("/data/Combined_hthymus/Fetal_Pediatric_...
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R
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## code to prepare `DATASET` dataset goes here library(RNHANES) library(plyr) library(dplyr) # NHANES 1999-2018 -------------------------------------------------------- #Demographic DEMO <- nhanes_load_data(c("DEMO","DEMO_B","DEMO_C","DEMO_D","DEMO_E","DEMO_F","DEMO_G","DEMO_H","DEMO_I","DEMO_J"), ...
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R
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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R
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############################################################ ## Project: Coordinated multicellular immune programs and drug targets revealed by single-cell analysis in driver-mutated NSCLC ## ## Purpose: ## Reproducible R workflow for single-cell analysis, TIME module identification, prognostic model construction, ...
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R
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#Prepare GWAS sumstats files #get summary file from FINNGEN #focus on congenital studies #grep "XVII Congenital" finngen_R11_manifest.tsv | cut -f1 > congenital_studies.txt #get other controls # grep "Crohn's" finngen_R11_manifest.tsv | cut -f1 > immune_studies.txt #get lupus # grep "SLE_FG" finngen_R11_manifest.tsv | ...
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R
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library("ggVennDiagram") library(eulerr) library("GeneOverlap") human_main_markers <- readxl::read_xlsx("tables/SigGenes_Main_CellTypes.xlsx", sheet = 1) mouse_main_markers <- readxl::read_xlsx("tables/Mouse_SigGenes_Main_CellTypes.xlsx", sheet = 1) mouse_main_markers_orthologs <- subset(mouse_main_markers, hgnc_symbol...
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R
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--- title: "Approach/Avoid Behavior Prep" output: html_document date: "`r format(Sys.time(), '%d %B, %Y')`" --- ```{r setup, include=FALSE} knitr::opts_chunk$set( echo <- FALSE, # don't print the code chunk warning <- FALSE, # don't print warnings message <- FALSE, # don't print messages fig.width <- 5, #...
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R
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# ------------- Figure 3 -------------- #----Figure 3A---- #Analysis of Cancer Cell Status #CopyKat Identify malignant cells rm(list = ls()) setwd("./t100553/wss") sce <- readRDS("./sce_Annotated_umap.rds") dir.create("./copykat/") setwd("./copykat") #corrsce <- readRDS("./subsce.corr.rds") epi <- subset(s...
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R
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--- title: "Granger Analyses" output: html_document date: "2025-02-11" --- ```{r setup, include=FALSE} ## libraries ## library(tidyverse) library(ggplot2) library(lmerTest) library(doParallel) library(parallel) library(foreach) library(here) library(fs) library(lmtest) library(scales) library(ggthemr) library(RColorBr...
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# NOTES ------------------------------------------------------------------- # Note that the function in scater gave negative values and # when cpm.DGEList was allowed to take the log itself all CPMs were nonzero! # ROTS, NOISeq, EBSeq, monocle, scDD have no log fold changes internally calculated? # DE TOOLS WRAPPER ...
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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R
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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R
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# Load libraries ## Libraries for basic preprocessing library(reshape2) library(dplyr) ## Single cell libraries library(Seurat) #library(pagoda2) ##library(conos) ## Libraries for plotting library(ggplot2) library(ggrepel) library(RColorBrewer) library(pheatmap) ## Annotation and pathway analysis library ##library(...
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--- title: "Ectoderm subclustering and annotation" output: html_document date: "2025-04-05" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(pat...
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R
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# ---- libs ---- library("arrow") # parquet files library("binom") # wilson confidence intervals for binomial counts library("foreach") # flexible looping and return amalgamation library("episensr") # misclassification error contingency table adjustments # library("simdata") # NORTA method to get correl...
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# plotParam ------------------------------------------------------------- #' @name plotParam #' @aliases plotParam #' @title Visualize distributional characteristics of RNA-seq experiment #' @description This function plots the results of the parameter estimation. This includes the absolute and relative sequencing dep...
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--- title: "Mesenchyme_subclustering_and_annotation" output: html_document date: "2025-04-05" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(p...
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--- title: "Mouse_Spatial_Expression" output: html_document date: "2025-04-17" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(patchwork) libra...
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R
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# Barnby et al. (2026): Corpus Callosum Dysgenesis impairs metacognition: # evidence from multi-modality and multi-cohort replications # # Analysis script covering three experiments: # Experiment 1: Online RDK (CCD vs NT, computer-based) # Experiment 2: In-lab RDK (CCD vs NT, MRI environment) # Experiment 3: VR ...
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R
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individual_and_overall_robust_lme_onset_before_turn_model_and_plot <- function(region, freq, distance_df, brain_df, plot_title, y_low, y_high, rerun_model = TRUE){ if(rerun_model == TRUE){ ## Run LME Multiple Regression Models with two predictors: Distance to Ghost, Points Remaining # merge be...
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# EVALUATE DISTRIBUTIONAL FITS -------------------------------------------- #' @name evaluateDist #' @aliases evaluateDist #' @title Model Diagnostics for RNAseq Data #' @description With this function, the user can determine goodness of fit for each gene. #' @usage evaluateDist(countData, batchData = NULL, #' spikeDa...
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--- title: "Species_Comparison" output: html_document date: "2025-04-09" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(patchwork) library(vir...
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R
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--- title: "CNCC subclustering and annotation" output: html_document date: "2025-04-06" --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(root.dir = "/scr1/users/manchela/Data") library(Seurat) library(SeuratDisk) library(tidyverse) library(harmony) library(dplyr) library(patchwo...