Description Usage Arguments Value
View source: R/process_counts_hash.R
This script reads in a counts file from either the DropSeq or 10x pipeline, converts the genes to a given naming convention (MGI or HGNC) and creates Seurat object from counts. It is the input for align_sers. This file also adds hashing information to a Seurat object and adds hash id to barcodes.
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directory |
directory containing the output files of align_dropseq_2.sh or cell ranger |
from_gene |
"ENSG" or "ENSMUSG" or "HGNC" or "MGI" |
to_gene |
"MGI" or "HGNC" |
hash_dir |
Directory containing hash counts files |
hash_meta |
csv file containing conversion of hash ID to sample name |
sample_id |
Optional experimental ID to prefix cell names |
type |
"DropSeq" or "10x" |
T_dir |
Optional directory to T cell TCR |
B_dir |
optional directory to B cell BCR |
umi_thresh |
Minimum total umi count for cells |
Outputs a Seurat file prepared to rPCA anchoring
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