Hi, I have a Canu assembly (Pacbio reads). I want to use arrow to polish my assembly but beforehand I want to subset my raw reads to have a coverage of around 80X. The output from pacbio was a single subreads.bam file with coverage of 150X. I read that polishing coverage above 100X does not really improve the quality, so I want to test different coverage values. My question is how to create a new BAM file from the original that has e.g 80X coverage and is compatible with pbalign/blasr. I found several posts saying that using samtools is not going to work as the BAM generated file does not contain all the info needed by blasr. Thanks, Myrsini