knitr::opts_chunk$set(
  collapse = TRUE,
  comment = "#>",
  fig.path = "man/figures/README-",
  out.width = "100%"
)

gcplyr

version <- as.vector(read.dcf('DESCRIPTION')[, 'Version'])
version <- gsub('-', '.', version)

packageversion CRAN status License: MIT

What this package can do

gcplyr was created to make it easier to import, wrangle, and do model-free analyses of microbial growth curve data, as commonly output by plate readers.

Please send all questions, requests, comments, and bugs to mikeblazanin [at] gmail [dot] com

Installation

You can install the version most-recently released on CRAN by running the following line in R:

install.packages("gcplyr")

You can install the most recently-released version from GitHub by running the following lines in R:

install.packages("devtools")
devtools::install_github("mikeblazanin/gcplyr")

Getting Started

The best way to get started is to read through the articles series, which breaks down a typical workflow using gcplyr from start to finish, starting with the introduction:

  1. Introduction: vignette("gc01_gcplyr")
  2. Importing and transforming data: vignette("gc02_import_reshape")
  3. Incorporating experimental designs: vignette("gc03_incorporate_designs")
  4. Pre-processing and plotting your data: vignette("gc04_preprocess_plot")
  5. Processing your data: vignette("gc05_process")
  6. Analyzing your data: vignette("gc06_analyze")
  7. Dealing with noise: vignette("gc07_noise")
  8. Best practices and other tips: vignette("gc08_conclusion")
  9. Working with multiple plates: vignette("gc09_multiple_plates")
  10. Using make_design to generate experimental designs: vignette("gc10_using_make_design")

Citation

Please cite software as:

Blazanin, M. gcplyr: an R package for microbial growth curve data analysis. BMC Bioinformatics 25, 232 (2024). https://doi.org/10.1186/s12859-024-05817-3



mikeblazanin/gcplyr documentation built on Jan. 18, 2025, 11:40 a.m.