Fig 2. Average read counts for each marker by input number of million sequence reads (log10) for human (hg38) datasets.

Red arrows indicate minimum read counts: 5 million (5×10⁶) reads for whole-exome sequencing and RNA sequencing and 100 million (1×10⁸) reads for whole-genome sequencing. The red horizontal line denotes the minimum average read counts of sex-specific marker sequences.