I am an undergrad, and fairly new to bioinformatic but I am working on assembling contigs from a metagenome. I know the basic principle behind IDBA is in each iteration short and low-depth contigs are removed iteratively based on cutoff threshold from low to high and iteratively increases the Kmer etc. I was wondering if there is there any way to obtain information on the regions of low depth? I imagine one of the output files could help me indoing so. Any and all help would be much appreciated.--Thanks in advance,Shan
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