Total reads: Total number of sequencing reads
Read length: The median number of alignable bases in read 1 (or read 2)
Fraction of Q30 bases: The fraction of total bases with quality score at least 30 for read 1 (or read 2)
Reads with valid barcodes: The number of reads that could be confidently associated with a valid barcode

Cells detected: The number of barcodes associated with partitions containing cells
Reads from cells: The number of reads with a valid barcode that are associated with cell-containing partitions
Total mapped de-duplicated reads in cells: Total number of reads that have mapping quality at least 30 and are not duplicates that are associated with cell-containing partitions
Median duplicate fraction per cell: Median over cells of the fraction of duplicate reads
Median effective reads per Mb: Median over cells of the number of reads per cell with mapping quality at least 30 and not duplicate divided by the genome size in megabases
Median average ploidy: Median of the average ploidy per cell distribution
Median estimated CNV resolution per cell: The approximate size of copy number events (in Mb) that can be profiled accurately in single cells based on the sequencing depth and library quality, as determined by a theoretical model
Fraction of noisy cells: Fraction of cells in the dataset that have high values of DIMAPD or where the copy number estimation procedure may be unreliable
Fraction of genome mappable: The fraction of 20kb bins of the genome that are at least 70% mappable