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arXiv:2610.37851 · v1

Evaluating and improving AI agents for sequencing protocol understanding

首次提交 2026-10-28 02:58
版本更新 2026-10-28 02:58
雷达观测 2026-10-30 10:23
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摘要

Existing scientific-agent benchmarks rarely evaluate whether agents can reconstruct the exact molecular structures and generation workflows specified by sequencing protocols, a capability critical for analyzing customized sequencing assays. We introduce LibStructBench, a document-grounded benchmark for reconstructing sequencing-library structures and molecular workflows. Our experiments show that frontier agents often produce approximately correct reconstructions but remain unreliable at exact reconstruction, particularly in molecular-state representation and workflow connectivity. Switching the underlying language model produced larger average performance differences than switching agent harnesses, with a statistically significant difference only for molecular-state reconstruction. Additional knowledge improved oligo-family recovery in a small pilot without improving mean molecular-workflow scores. Autonomous accumulation of procedural rules and cross-protocol examples showed non-monotonic validation performance and no mean held-out molecular-workflow improvement in the tested trajectory. These findings highlight the need for more controlled and verifiable approaches to scientific reasoning about molecular processes in complex experimental protocols.

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v1 · 2026-10-28 02:58 · 最新观测版本

Evaluating and improving AI agents for sequencing protocol understanding

Existing scientific-agent benchmarks rarely evaluate whether agents can reconstruct the exact molecular structures and generation workflows specified by sequencing protocols, a capability critical for analyzing customized sequencing assays. We introduce LibStructBench, a document-grounded benchmark for reconstructing sequencing-library structures and molecular workflows. Our experiments show that frontier agents often produce approximately correct reconstructions but remain unreliable at exact reconstruction, particularly in molecular-state representation and workflow connectivity. Switching the underlying language model produced larger average performance differences than switching agent harnesses, with a statistically significant difference only for molecular-state reconstruction. Additional knowledge improved oligo-family recovery in a small pilot without improving mean molecular-workflow scores. Autonomous accumulation of procedural rules and cross-protocol examples showed non-monotonic validation performance and no mean held-out molecular-workflow improvement in the tested trajectory. These findings highlight the need for more controlled and verifiable approaches to scientific reasoning about molecular processes in complex experimental protocols.

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