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Does the phrase "contigs from different samples" refer to contigs co-assembled from reads derived from different sequencing samples? If so, you can generate a coverage file according to the "Coverage Profile" section in the README to use as input for the subsequent steps. The 'path_to_sequencing_reads/*fastq' should include all the sequencing samples.
Hi,
thanks a lot for your work.
I want to know how I can use metabinner to bin the contigs combined from different samples?
Sincerely,
Gia
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