| perform_qc | R Documentation | 
Perform QC step on single cells and bins.
perform_qc(Y_raw, sampname_raw, ref_raw, QCmetric_raw,
        cov_thresh = 0, minCountQC = 20, 
        mapq20_thresh = 0.3, mapp_thresh = 0.9,
        gc_thresh = c(20, 80), nMAD = 3)
| Y_raw | raw read count matrix returned
from  | 
| sampname_raw | sample names for quality control returned
from  | 
| ref_raw | raw GRanges object with corresponding GC content
and mappability for quality control returned from
 | 
| QCmetric_raw | a QC metric for single cells returned from
 | 
| cov_thresh | scalar variable specifying the lower bound of read count
summation of each cell. Default is  | 
| minCountQC | the minimum read coverage required for
normalization and EM fitting. Defalut is  | 
| mapq20_thresh | scalar variable specifying the lower threshold
of proportion of reads with mapping quality greater than 20.
Default is  | 
| mapp_thresh | scalar variable specifying mappability of
each genomic bin. Default is  | 
| gc_thresh | vector specifying the lower and upper bound of
GC content threshold for quality control. Default is  | 
| nMAD | scalar variable specifying the number of MAD from the median
of total read counts adjusted by library size for each cell.
Default is  | 
A list with components
| Y | read depth matrix after quality control | 
| sampname | sample names after quality control | 
| ref | A GRanges object specifying whole genomic bin positions after quality control | 
| QCmetric | A data frame of QC metric for single cells after quality control | 
Rujin Wang rujin@email.unc.edu
Y_raw <- coverageObj.scopeDemo$Y
sampname_raw <- rownames(QCmetric.scopeDemo)
ref_raw <- ref.scopeDemo
QCmetric_raw <- QCmetric.scopeDemo
qcObj <- perform_qc(Y_raw = Y_raw, sampname_raw = sampname_raw,
                ref_raw = ref_raw, QCmetric_raw = QCmetric_raw)
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