This guide shows how to publish DNA-derived spatiotemporal biodiversity data and make it discoverable through national and global biodiversity data discovery platforms. Based on experiences from Australia, Norway, Sweden, UNITE, and GBIF.
This is the case for most metagenomics, metabarcoding and eDNA studies.
Comment:
I am not sure if this holds really true for MOST metabarcoding studies. There are many studies utilizing only part of a specimen, or even the fixative of a bulk sample. As such, the potential specimen can be located in a bulk sample, but I agree that no safe link between specimen and sequence exists (contrary to as when DNA barcoding a single specimen).
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