What is the recommended minimum read coverage for Cleanplex UMI NGS panels?

The suggested minimum read coverage is 7,500 paired-end reads/ amplicon/ nanogram of DNA input for detection of 0.1% allele frequency, when the minimum DNA input amount is also met. 7,500 paired-end reads equates to 3,750 clusters or single-end reads on the sequencing chip. Please see FAQ for DNA input requirement for detecting 0.1% somatic variant frequency.