Evidence map›Paper›PMID 34222831›Full record

ArticleSIAM journal on mathematics of data science2020

Persistent Cohomology for Data With Multicomponent Heterogeneous Information.

Zixuan Cang, Guo-Wei Wei

Abstract read
In one paragraph

Article in SIAM journal on mathematics of data science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Review
  3. PERSISTENT SHEAF LAPLACIANS.Foundations of data science (Springfield, Mo.) · 2025
    Article
  4. Article
  5. Article
  6. PERSISTENT HYPERDIGRAPH HOMOLOGY AND PERSISTENT HYPERDIGRAPH LAPLACIANS.Foundations of data science (Springfield, Mo.) · 2023
    Article
  7. Review
  8. Article
  9. Path Topology in Molecular and Materials Sciences.The journal of physical chemistry letters · 2023
    Article
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

2 authors.

Zixuan CangDepartment of Mathematics, Michigan State University, East Lansing, MI 48824.
Guo-Wei WeiDepartment of Mathematics, Department of Biochemistry and Molecular Biology, Department of Electrical and Computer Engineering, Michigan State University, East Lansing, MI, 48824.

Funding

Synergistic integration of topology and machine learning for the predictions of protein-ligand binding affinities and mutation impactsR01GM126189 · NIGMS · MICHIGAN STATE UNIVERSITY · PI WEI, GUOWEI · 2018 to 2021
$1.4M
NIGMS NIH HHS R01 GM126189
6 · The paper itself

Abstract

Persistent homology is a powerful tool for characterizing the topology of a data set at various geometric scales. When applied to the description of molecular structures, persistent homology can capture the multiscale geometric features and reveal certain interaction patterns in terms of topological invariants. However, in addition to the geometric information, there is a wide variety of nongeometric information of molecular structures, such as element types, atomic partial charges, atomic pairwise interactions, and electrostatic potential functions, that is not described by persistent homology. Although element-specific homology and electrostatic persistent homology can encode some nongeometric information into geometry based topological invariants, it is desirable to have a mathematical paradigm to systematically embed both geometric and nongeometric information, i.e., multicomponent heterogeneous information, into unified topological representations. To this end, we propose a persistent cohomology based framework for the enriched representation of data. In our framework, nongeometric information can either be distributed globally or reside locally on the datasets in the geometric sense and can be properly defined on topological spaces, i.e., simplicial complexes. Using the proposed persistent cohomology based framework, enriched barcodes are extracted from datasets to represent heterogeneous information. We consider a variety of datasets to validate the present formulation and illustrate the usefulness of the proposed method based on persistent cohomology. It is found that the proposed framework outperforms or at least matches the state-of-the-art methods in the protein-ligand binding affinity prediction from massive biomolecular datasets without resorting to any deep learning formulation.

Indexed as

55U1055U3092C40biophysicsdrug designmachine learningtopological data analysis

Identifiers

PMID34222831
PMCPMC8249079

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.