Evidence map›Paper›PMID 37490457›Full record

ArticleBioinformatics (Oxford, England)2023

CSI: Contrastive data Stratification for Interaction prediction and its application to compound-protein interaction prediction.

Apurva Kalia, Dilip Krishnan, Soha Hassoun

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. 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

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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

3 authors.

Apurva KaliaDepartment of Computer Science, Tufts University, Medford, MA 02155, United States.
Dilip KrishnanGoogle Research, Cambridge, MA 02142, Unites States.
Soha HassounDepartment of Computer Science, Tufts University, Medford, MA 02155, United States.ORCID 0000-0001-9477-2199

Funding

Computational Techniques for Advancing Untargeted Metabolomics AnalysisR01GM132391 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI HASSOUN, SOHA · 2019 to 2022
$1.5M
Deep Learning Models for Metabolomics AnalysisR35GM148219 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI Soha Hassoun · 2023 to 2026
$1.4M
NIGMS NIH HHS R01 GM132391NIGMS NIH HHS R35 GM148219NIH HHS R01GM132391
6 · The paper itself

Abstract

motivationAccurately predicting the likelihood of interaction between two objects (compound-protein sequence, user-item, author-paper, etc.) is a fundamental problem in Computer Science. Current deep-learning models rely on learning accurate representations of the interacting objects. Importantly, relationships between the interacting objects, or features of the interaction, offer an opportunity to partition the data to create multi-views of the interacting objects. The resulting congruent and non-congruent views can then be exploited via contrastive learning techniques to learn enhanced representations of the objects.

resultsWe present a novel method, Contrastive Stratification for Interaction Prediction (CSI), to stratify (partition) a dataset in a manner that can be exploited via Contrastive Multiview Coding to learn embeddings that maximize the mutual information across congruent data views. CSI assigns a key and multiple views to each data point, where data partitions under a particular key form congruent views of the data. We showcase the effectiveness of CSI by applying it to the compound-protein sequence interaction prediction problem, a pressing problem whose solution promises to expedite drug delivery (drug-protein interaction prediction), metabolic engineering, and synthetic biology (compound-enzyme interaction prediction) applications. Comparing CSI with a baseline model that does not utilize data stratification and contrastive learning, and show gains in average precision ranging from 13.7% to 39% using compounds and sequences as keys across multiple drug-target and enzymatic datasets, and gains ranging from 16.9% to 63% using reaction features as keys across enzymatic datasets. AVAILABILITY AND IMPLEMENTATION: Code and dataset available at https://github.com/HassounLab/CSI.

Indexed as

Drug Delivery SystemsMetabolic EngineeringAmino Acid SequenceProbabilitySynthetic Biology

Identifiers

PMID37490457
PMCPMC10423023

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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.