All curated genomic sequences and the criteria used for determining their inclusion or exclusion.

For each species, we provide the unique sequence identifier (column D), the reason for inclusion or exclusion (columns H-J), the sequence length, the length of the contig on which the putative LTG is placed (column H), the accession of the genomic data, and whether the sequence hit closely-related species or multiple other CDS on the contig hit closely-related species (columns I,J). Any notable literature pertaining to the sequence or GF is noted in the “other” column. (XLSX)