First of all, that's not actually what the paper said. Quoting what the mathematician's analysis actually said, bolding the parts you skipped over that I think are crucially important:
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At this point, the contig with the identification k141_27232, with which 1,407,705 sequences are associated, and thus about 5% of the remaining 26,108,482 sequences, should be discussed in detail. Alignment with the nucleotide database on 05/12/2021 showed a high match (98.85%) with "Homo sapiens RNA, 45S pre- ribosomal N4 (RNA45SN4), ribosomal RNA" (GenBank: NR_146117.1, dated 04/07/2020).
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The point is that this remaining 5% of the sequences, comprising a total of 1,407,705 sequences, all belongs to a single contig, with the identification of k141_27232. It strongly suggests that this contig, far from being viral in nature, was actually -human- in nature. The mathematician even goes so far as to name the specific human component that it has such a high match with:
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"Homo sapiens RNA, 45S pre- ribosomal N4 (RNA45SN4), ribosomal RNA" (GenBank: NR_146117.1, dated 04/07/2020).
I didn't skip over anything.
You didn't quote the parts I bolded. That's what I meant. If you were on my side, you'd probably have called it "cherry picking", but I acknowledge that you may have just thought those parts weren't important.
Why would I quote your cherry picked parts.
The parts I bolded were the parts you skipped. I think they were important, which is why I took the time include and bold them.
I already addressed it. It is 1 contig out of 28,459. It is statistically meaningless.
Do you have any evidence that it was "meaningless"? For my part, I doubt the mathematician would have spent so much time on it if it was as you say. I suspect the reason he finds it so important is because it was both the longest contig found and it also closely matched a human RNA sequence, as I mentioned in the nested quote above.