Hi all, I am doing BLASTN to look for AMR genes in my contigs assembled from shotgun metagenome sequence reads. The BLAST results show the same query sequence matching against different variants of a same gene; all of them with the same stats as shown in the example below. What would be the best approach going forward in this scenario? Do I just group all of them as a single hit to the OXA gene (despite the differences between the variants) , or consider each hit as an individual match and include all of them in my results?
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The top 10 hits are all OXA genes, and the matches are all significant, high subject coverage, and high identity. But the query coverage isn't as high -- only positions 107 through 934 are aligned, but the sequence has another 900 bases left. So it appears that at the very least this sequence is an OXA-something.
You could search against a more general database also (I presume your subject database is enriched for AMR sequences?) to see if something comes up that matches the remainder of the sequence.