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API-BLEND: A Comprehensive Corpora for Training and Benchmarking API LLMs

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arxiv 2402.15491 v2 pith:BJPN47LK submitted 2024-02-23 cs.CL cs.AI

classification cs.CLcs.AI
keywords api-blendapisdatasetsllmstrainingbenchmarkingcorporacurating
verification ladder T0 review T1 audit T2 compute T3 formal
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There is a growing need for Large Language Models (LLMs) to effectively use tools and external Application Programming Interfaces (APIs) to plan and complete tasks. As such, there is tremendous interest in methods that can acquire sufficient quantities of train and test data that involve calls to tools / APIs. Two lines of research have emerged as the predominant strategies for addressing this challenge. The first has focused on synthetic data generation techniques, while the second has involved curating task-adjacent datasets which can be transformed into API / Tool-based tasks. In this paper, we focus on the task of identifying, curating, and transforming existing datasets and, in turn, introduce API-BLEND, a large corpora for training and systematic testing of tool-augmented LLMs. The datasets mimic real-world scenarios involving API-tasks such as API / tool detection, slot filling, and sequencing of the detected APIs. We demonstrate the utility of the API-BLEND dataset for both training and benchmarking purposes.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. DICE-BENCH: Evaluating the Tool-Use Capabilities of Large Language Models in Multi-Round, Multi-Party Dialogues

    cs.CL 2025-06 conditional novelty 7.0 of 10

    A new benchmark and metric show that large language models still struggle to call tools when the needed details are scattered across multi-party, multi-round group dialogues.

  2. An Auditable Agent Platform For Automated Molecular Optimisation

    cs.LG 2025-08 conditional novelty 5.0 of 10

    A hierarchical multi-agent LLM platform with recorded provenance improved average predicted binding affinity for AKT1 by 31%, while single-agent runs favored drug-likeness.

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