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Regarding the perfect, strict, and loose hits, Jia et al. 2017 mentions:
The RGI currently supports two detection model types (Protein Homolog and Protein Variant) and analyzes sequences under three paradigms—Perfect, Strict, and Loose (a.k.a. Discovery). The Perfect algorithm is most often applied to clinical surveillance as it detects perfect matches to the curated reference sequences and mutations in CARD.
Could you provide a more technical definition of these terms? For instance for 'perfect', I understand from #101 that the self-mapping bit-scores determine the 'perfect' hits. Could you provide more info on how 'strict' and 'loose' thresholds are chosen?
Thanks in advance,
Ali
The text was updated successfully, but these errors were encountered:
@alimayy As an example, Blasting AXC-1 on the CARD database produces the results shown. The bit-score chosen will be 500, as it will capture genes similar to AXC-1.
A Perfect hit to AXC-1 has all amino acids matching CARD reference.
A Strict hit to AXC-1 will be any gene with at least bitscore of 500.
A Loose hit to AXC-1 will be any gene with bitscore below 500.
Hi there,
Thanks for developing RGI.
Regarding the perfect, strict, and loose hits, Jia et al. 2017 mentions:
Could you provide a more technical definition of these terms? For instance for 'perfect', I understand from #101 that the self-mapping bit-scores determine the 'perfect' hits. Could you provide more info on how 'strict' and 'loose' thresholds are chosen?
Thanks in advance,
Ali
The text was updated successfully, but these errors were encountered: