Rundf_dna | R Documentation |
Run all steps for scDNA-seq data
Rundf_dna( alt_all = NULL, ref_all = NULL, var_all = NULL, samplename = "sample", genome_assembly = "GRCh38", dir_path = "./", barcodes = NULL, size = NULL, assay = "scDNAseq", raw_counts = NULL, ref_counts = NULL, type = "tumor", cell_filter = 5, SNP_filter = 10, min_vaf = 0, max_vaf = 1 )
alt_all |
A SNP by cell read count matrix/ spare matrix for the alternative alleles. |
ref_all |
A SNP by cell read count matrix/ spare matrix for the reference alleles. |
samplename |
Sample name for the data. |
genome_assembly |
The genome assembly used for sequencing alignment. (ex: "GRCh38" or "GRCh37") |
dir_path |
Path of the output directory. |
barcodes |
A matrix/ data.frame with barcodes for each cell in the first column. |
size |
A numeric vector for the size (bp) of different chromosomes (with the names indicating which chromosome from 1 to 22) |
assay |
A character indicating the type of sequencing data. (ex: "scDNAseq" or "scATACseq") |
raw_counts |
A large binned coverage matrix (m1 bin by n1 cell) for all chromosomal regions of tumor sample. |
ref_counts |
A large binned coverage matrix (m2 bin by n2 cell) for all chromosomal regions of normal sample. |
type |
Specify whethere the sample is a "tumor" or "cellline". If "type" is a "cellline", param "ref_counts" needs to be specified for normal sample. |
cell_filter |
An integer of minimum cell number for SNP selection. |
SNP_filter |
An integer of minimum SNP number for cell selection. |
min_vaf |
A numerical value in the range (0,1) of minimum SNP variant allele frequency in the pseudo bulk for SNP selection. |
max_vaf |
A numerical value in the range (0,1) of mzsimum SNP variant allele frequency in the pseudo bulk for SNP selection. |
vcf_all |
A matrix/ data.frame of the vcf format for SNP information. (The length and order are the same as nrow(alt_all) and nrow(alt_all)) |
A Alleloscope object including the necessary information.
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