miso
, short for microbiome software is a collection of helpers that we use to analyze microbiome data. It makes it easier to run some common analyses and is pretty opinionated towards our own experiences.
miso
is simply a one stop location for smaller analysis helper and visualizations we often use in the lab. It is supposed to remove some common pain points we encountered or to implement custom (mostly genomic) analysis steps.
At this point complex workflows in the lab have been ported to nextflow and are no longer included here. See our pipelines for this.
For misos
an analysis step is based on input data and a configuration, thus having the function signature step(object, config)
. Most steps can be chained with the pipe operator. For instance, the following is possible with miso
:
library(miso)
config <- list(
demultiplex = config_demultiplex(barcodes = c("ACGTA", "AGCTT")),
preprocess = config_preprocess(truncLen = 200),
denoise = config_denoise()
)
output <- find_read_files("raw") %>%
demultiplex(config$demultiplex) %>%
quality_control() %>%
preprocess(config$preprocess) %>%
denoise(config$denoise)
This clearly logs the used workflow and the configuration. The configuration can also be saved and read in many formats, for instance yaml.
config.yaml:
preprocess:
threads: yes
out_dir: preprocessed
trimLeft: 10.0
truncLen: 200.0
maxEE: 2.0
denoise:
threads: yes
nbases: 2.5e+08
pool: no
bootstrap_confidence: 0.5
taxa_db: https://zenodo.org/record/1172783/files/silva_nr_v132_train_set.fa.gz?download=1
species_db: https://zenodo.org/record/1172783/files/silva_species_assignment_v132.fa.gz?download=1
hash: yes
This can now be reused by someone else:
config <- read_yaml("config.yml")
output <- find_read_files("raw") %>%
quality_control() %>%
preprocess(config$preprocess) %>%
denoise(config$denoise)