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开发阶段案例 · 模型盲评尚待独立人工复核,不代表正式 Benchmark 结论。
自动补全无 Evidence 更优2 / 162 · e6bfbd7a9561cfcb

Bridging from single to collective cell migration: A review of models and links to experiments

定量生物学 · 2011.10873v1

FLOWING EVIDENCE BENCHMARK

怎么判断 Evidence 真的有帮助?

核心问题是:在同一写作位置、使用同一模型和任务时,提供检索文献片段会怎样改变首次输出?我们成对比较两种条件,保留持平、不可用和评审未完成的结果。

同一段原稿 · 比较是否提供 Evidence

01 · 固定写作位置

论文原稿

同一处写作点位 ▌

同一原稿位置的自动补全成对比较

02 · 构造两组输入

两组共用

原稿上下文、模型、任务和提示词

A · 提供 Evidence

额外提供检索文献片段

B · 不提供 Evidence

不提供检索文献片段

LLM

同一模型、同一版本

A → 首次输出

B → 首次输出

盲评 Agent

匿名标记两份首次输出为 X、Y

按续写质量判断:准确性、任务贴合度和可用性
输出:X 更优 / 持平 / Y 更优 / 两组均不可用

换序复评:X / Y → Y / X

盲评具体怎么判?

① 匿名两份输出
评审看到同一原稿和两份首次输出,但不知道哪份用了 Evidence。

② 比较并换序复评
根据当前任务的标准,按 X/Y、再按 Y/X 的顺序各评一次。

③ 复核分歧
两次结论不一致时再做第三次判定;未完成的评审也留在分母。

自动补全点位怎样分层?

在查看生成结果前,先核查检索片段是否含有能直接支撑下一步续写的具体命题;有则放在左侧机会组,否则放在右侧普通组。每个学科从可准入论文中均衡选取两组点位。50/50 是实验设计,不代表真实写作中两类点位各占一半。

AUTOCOMPLETE · 110

定量生物学、统计学、天体物理学

左侧 55 个、右侧 55 个点位;统计学采用 10 篇论文的复测结果。

AUTOCOMPLETE · 52

心理学与气候科学

左侧 26 个、右侧 26 个点位;心理学计入 9 篇,气候科学计入 4 篇。

表格里的百分比怎么算?

五学科共有 81 个左侧点位,其中 51 个点位的 Evidence 版本获评更优。持平、两组均不可用和评审未完成的点位仍计入分母。

51Evidence 版本更优
÷
81该层全部点位
=
63%该层 Evidence 获评更优的比例

来源贡献是另一项复核:已进入复核的 22 个 Evidence 获胜点位中,16 个确认直接使用了检索论文;另有 29 个胜出点位尚待复核。

当前是开发阶段的模型评审结果,尚未完成独立人工复核;这些数字不代表正式 Benchmark 结论,也不能单独证明因果关系。

原稿写作位置

原文摘录 · 非 PDF 页面

研究论文 · 原文片段

Bridging from single to collective cell migration: A review of models and links to experiments

5 Discussion

Overall, more experimental papers that probe the circuits that get recruited in the collective cell migration are needed. The papers [ 129 , 173 ] on the Merlin-Rac loop and on the link to YAP and E-cadherin [ 173 ] should be followed up with more detailed computational modeling and future rounds of experiments.

…l targets, and Fig 4 summarizes the ranges of relevance of both computational and experimental methods. Our review has focused on the topic of single and collective cell migration and its regulation. Likely motivated by development of disease therapies and NIH funding, or drug targets and support from pharmaceutical companies, the more medically oriented subjects such as cancer, liver toxicity, or lung morphogenesis, have fostered many generations of computational models. By comparison, the level of basic scientific computational research on multiscale cell biology modeling is still emerging.

↓ 此处生成下一段续写

黄色标出写作点位附近的原文;本页根据评测输入重排文本,不是原始 PDF 截图。

同一写作位置的成对对照盲评结果:无 Evidence 更优

两组使用同一模型、同一写作任务和原稿上下文,仅比较是否提供检索文献片段。下方展示评测记录中的首次输出。

Evidence

同一模型与写作位置 · 提供检索文献片段 · 首次输出

本次未获偏好

The models reviewed here span a wide range of spatial and temporal scales, from stochastic descriptions of individual cell motion to continuum and agent-based treatments of collective migration. Bridging these scales remains a central challenge, since the parameters that govern single-cell behavior are not always the ones that determine tissue-level patterns.

提供给 Evidence 版本的文献片段

100 years after Smoluchowski: stochastic processes in cell biology

We reviewed here the influential Smoluchowski equation and its applications in modeling, analysis in biophysics and computational cell biology.

无 Evidence

同一模型与写作位置 · 不提供检索文献片段 · 首次输出

盲评更优

This imbalance suggests that the choice of biological application, rather than the intrinsic multiscale character of the migration problem, has largely driven the development of computational models in this field. A more balanced research portfolio would couple the medically motivated models to equally detailed basic-science studies of the underlying migratory machinery.

模型盲评结论

模型盲评判定“无 Evidence 更优”。下方保留评审原始理由(英文),供核对判断依据。

查看模型评审原始理由(英文)

Output A is fully grounded in the draft. It continues the contrast between medically-oriented computational research (cancer, liver toxicity, lung morphogenesis) and basic scientific computational research on multiscale cell biology, noting this imbalance and suggesting a more balanced approach. Every element traces to the draft's explicit claims about funding motivations and the emerging state of basic scientific computational research. Output B introduces unsupported claims: (1) 'stochastic descriptions of individual cell motion' - the source mentions 'stochastic processes' and the Smoluchowski equation but not individual cell motion in migration; (2) 'continuum and agent-based treatments of collective migration' - not mentioned in draft or source; (3) 'parameters that govern single-cell behavior are not always the ones that determine tissue-level patterns' - a substantive mechanistic claim about parameter relationships across scales with no support in the provided materials; (4) 'Bridging these scales remains a central challenge' - evaluative claim not grounded in the draft. The draft mentions 'multiscale cell biology modeling' as an emerging field but does not describe what scales are bridged, what methods are used, or what challenges exist. Output B reads as generic computational biology commentary rather than continuation of this specific manuscript's argument about funding imbalances.

文献片段是输入材料;出现于此不代表输出使用了它,也不代表它能够支持全部主张。原文与检索片段经过截取;页面没有展示模拟分数或模拟 PDF。