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Laurentiu Lupu MD's avatar

One detail in the Robin paper supports your argument almost in passing. Robin proposed photoreceptor outer segments and primary RPE; the lab used beads and ARPE-19 instead, for availability and speed. The laboratory’s constraints changed the proposed experiment before testing began.

The ranking that shaped which candidates reached the screen was built on different grounds: scientific rationale, pharmacological profile, and the supporting literature. It was assessed against expert preference and its own consistency.

If candidate generation grows faster than experimental capacity, the tested fraction will shrink, and the ranking will decide more of what ever meets an assay.

That can be tested within the same screen. Carry two or three lower-ranked candidates alongside the top set and repeat the comparison across screens. The difference in hit rates would show whether the ranking adds experimental enrichment beyond its agreement with expert judgment.

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