Description Usage Arguments Examples
View source: R/qc_and_filter.R
This function allows you to provide a list of paths leading to the QC sample sheet (Erica's pipeline Step 4) to perform quality control and filtering.
1 2 3 4 5 6 7 8 9 10 | qc_and_filter(
directories,
genome = "GRCh38",
suffix = "default",
min.umis = 500,
min.genes = 250,
max.mito = 0.3,
sig = T,
dense = F
)
|
directories |
List of directories containing CellRanger output for QC and filtering. Example single directory path is "/Volumes/broad_vangalenlab/depasquale/CellRanger/210628_GeneCounts" |
genome |
Desired genome: "GRCh38" and "GRCm38" are accepted, default is "GRCh38" |
suffix |
Suffix for directory where the output of this function will be stored and where the input sample sheet is located. Default is the "QC" suffix. |
min.umis |
QC filter for minimum number of Unique Molecular Identifiers (UMIs) detected per cell. Default is 500 |
min.genes |
QC filter for minimum number of genes detected per cell. Default is 250 |
max.mito |
QC filter to remove cells that exceed this fraction of mitochondrial alignments. Default is 0.3 |
sig |
Boolean for whether or not to plot cell type signatures. Default is T |
dense |
Boolean for whether or not to save dense matrices alongside sparse matrices. Default is F |
1 |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.