Table III.

Summary of sequencing data in the panel for 556 samples.

Variable	Outcome
Total no. of reads	118,156,518
Reads mapped to the amplicons (forward primer)	110,440,487
Reads mapped to the amplicons (reverse primer)	108,812,285
Reads mapped to the amplicon targets	105,107,193
Reads mapped to each amplicon (average)	3,892,859
Reads mapped to each sample per amplicon (mean)	7,001.5
Reads enrichment to the targets,% (average)	89
Uniformity of coverage, % (20% mean)	98
Total no. of variants among 46 point mutations	363