Evidence map›Paper›PMID 38745436›Full record

ArticleBioinformatics (Oxford, England)2024

Genotype sampling for deep-learning assisted experimental mapping of a combinatorially complete fitness landscape.

Andreas Wagner

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Andreas WagnerDepartment of Evolutionary Biology and Environmental Studies, University of Zurich, 8057 Zurich, Switzerland.ORCID 0000-0003-4299-3840

Funding

Swiss National Science Foundation 310030_208174
6 · The paper itself

Abstract

motivationExperimental characterization of fitness landscapes, which map genotypes onto fitness, is important for both evolutionary biology and protein engineering. It faces a fundamental obstacle in the astronomical number of genotypes whose fitness needs to be measured for any one protein. Deep learning may help to predict the fitness of many genotypes from a smaller neural network training sample of genotypes with experimentally measured fitness. Here I use a recently published experimentally mapped fitness landscape of more than 260 000 protein genotypes to ask how such sampling is best performed.

resultsI show that multilayer perceptrons, recurrent neural networks, convolutional networks, and transformers, can explain more than 90% of fitness variance in the data. In addition, 90% of this performance is reached with a training sample comprising merely ≈103 sequences. Generalization to unseen test data is best when training data is sampled randomly and uniformly, or sampled to minimize the number of synonymous sequences. In contrast, sampling to maximize sequence diversity or codon usage bias reduces performance substantially. These observations hold for more than one network architecture. Simple sampling strategies may perform best when training deep learning neural networks to map fitness landscapes from experimental data. AVAILABILITY AND IMPLEMENTATION: The fitness landscape data analyzed here is publicly available as described previously (Papkou et al. 2023). All code used to analyze this landscape is publicly available at https://github.com/andreas-wagner-uzh/fitness_landscape_sampling.

Indexed as

Deep LearningGenotypeNeural Networks, ComputerGenetic FitnessProteinsProteins

Identifiers

PMID38745436
PMCPMC11132821

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LicenceCC BY
Read underepoch 390

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.