A use case starts with a research question and your data, then explains the evidence we plan to gather, any model comparisons already collected and what they can establish for your decision.
You already know a model and want its evaluations, configurations and how to run it.
Research relevance and clinical evidence
Each question states its setting, endpoint and transfer limitations. A relevant assay result does not by itself establish clinical performance. Clinical research pages explain which patient or workflow questions the available evidence leaves unanswered.
Which retrieval configurations merit validation when molecular formula is unknown and a researcher can examine only a short list of candidate structures?
You bring
MS/MS spectra with metadata sufficient to derive neutral molecular mass
A frozen set of candidate molecular structures; the true identity must be present for the measured retrieval endpoint
Opens with 4 evaluated endpoints · 6 tested configurations · Proxy evidence only, plus limitations and sources.
User questions lead evidence gathering. A question can enter this collection before model comparisons have been collected: its plan states what to compare, how to validate it and what to collect next.
Where reviewed evidence is available, inspect the exact configurations, evaluation protocols and source-linked results. Incompatible protocols remain separate. Review method, research or clinical research scope, and missing evidence stay visible.