LGMLSep 28, 2018

Target-Independent Active Learning via Distribution-Splitting

arXiv:1809.10962v21 citations
AI Analysis

This work addresses a bottleneck in active learning for reducing label complexity, offering a more robust method that is less dependent on initial hypotheses, though it appears incremental in improving upon existing volume-splitting techniques.

The paper tackles the target-dependent label complexity gap in Agnostic Active Learning by introducing a novel notion of number density to map hypothesis distribution, proposing a target-independent distribution-splitting strategy that reduces label complexity and error rate with theoretical guarantees, and developing an application algorithm called DA^2 that shows effectiveness in experiments.

To reduce the label complexity in Agnostic Active Learning (A^2 algorithm), volume-splitting splits the hypothesis edges to reduce the Vapnik-Chervonenkis (VC) dimension in version space. However, the effectiveness of volume-splitting critically depends on the initial hypothesis and this problem is also known as target-dependent label complexity gap. This paper attempts to minimize this gap by introducing a novel notion of number density which provides a more natural and direct way to describe the hypothesis distribution than volume. By discovering the connections between hypothesis and input distribution, we map the volume of version space into the number density and propose a target-independent distribution-splitting strategy with the following advantages: 1) provide theoretical guarantees on reducing label complexity and error rate as volume-splitting; 2) break the curse of initial hypothesis; 3) provide model guidance for a target-independent AL algorithm in real AL tasks. With these guarantees, for AL application, we then split the input distribution into more near-optimal spheres and develop an application algorithm called Distribution-based A^2 (DA^2). Experiments further verify the effectiveness of the halving and querying abilities of DA^2. Contributions of this paper are as follows.

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