Closed-Form Test Functions for Biophysical Sequence Optimization Algorithms

Samuel Stanton, Robert Alberstein, Nathan Frey, Andrew Watkins, Kyunghyun Cho
6/28/2024
cs.LGcs.NE

No official code found. Best implementation: prescient-design/holo-bench (24 stars, MIT, last commit 2026-04-15).

Abstract

There is a growing body of work seeking to replicate the success of machine learning (ML) on domains like computer vision (CV) and natural language processing (NLP) to applications involving biophysical data. One of the key ingredients of prior successes in CV and NLP was the broad acceptance of difficult benchmarks that distilled key subproblems into approachable tasks that any junior researcher could investigate, but good benchmarks for biophysical domains are rare. This scarcity is partially due to a narrow focus on benchmarks which simulate biophysical data; we propose instead to carefully abstract biophysical problems into simpler ones with key geometric similarities. In particular we propose a new class of closed-form test functions for biophysical sequence optimization, which we call Ehrlich functions. We provide empirical results demonstrating these functions are interesting objects of study and can be non-trivial to solve with a standard genetic optimization baseline.

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Code Implementations(1)

MIT

Benchmark for Biophysical Sequence Optimization Algorithms

246PythonMay 10, 20246 months agoMIT
black-box-optimizationmachine-learningprotein-design

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Cite this paper

@article{stanton2024closedform,
  title  = {Closed-Form Test Functions for Biophysical Sequence Optimization Algorithms},
  author = {Samuel Stanton and Robert Alberstein and Nathan Frey and Andrew Watkins and Kyunghyun Cho},
  year   = {2024},
  eprint = {2407.00236},
  archivePrefix = {arXiv},
  url    = {http://arxiv.org/abs/2407.00236v1}
}

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