Hi, I am new to Pacbio sequence (sequel) analysis. I am trying to do a denovo assembly for a test data set (used subreads.fastq). I managed to construct an assembly using wtdbg2. I also ran wtdbg-cns to get consensus assembly, consensus.fa (*.lay.gz as input). However, I completely lost the way when I started to use quiver. It needs an aligned bam file. I am not sure how to get that from wtdbg2. any idea how to get that? thanks in advance Shri
wtdbg2
is an assembler. You will need to use an aligner to get the aligned BAM file from your original data. @h.mon has recommendations for that below.