Evidence map›Paper›PMID 36959450›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Persistent Homology for RNA Data Analysis.

Kelin Xia, Xiang Liu, JunJie Wee

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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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.

Kelin XiaDivision of Mathematical Sciences, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, Singapore. xiakelin@ntu.edu.sg.
Xiang LiuDivision of Mathematical Sciences, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, Singapore.
JunJie WeeDivision of Mathematical Sciences, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular representations are of great importance for machine learning models in RNA data analysis. Essentially, efficient molecular descriptors or fingerprints that characterize the intrinsic structural and interactional information of RNAs can significantly boost the performance of all learning modeling. In this paper, we introduce two persistent models, including persistent homology and persistent spectral, for RNA structure and interaction representations and their applications in RNA data analysis. Different from traditional geometric and graph representations, persistent homology is built on simplicial complex, which is a generalization of graph models to higher-dimensional situations. Hypergraph is a further generalization of simplicial complexes and hypergraph-based embedded persistent homology has been proposed recently. Moreover, persistent spectral models, which combine filtration process with spectral models, including spectral graph, spectral simplicial complex, and spectral hypergraph, are proposed for molecular representation. The persistent attributes for RNAs can be obtained from these two persistent models and further combined with machine learning models for RNA structure, flexibility, dynamics, and function analysis.

Indexed as

Data AnalysisRNARNAMachine learningMolecular representationPersistent homologyPersistent spectralRNA data analysisSimplicial complexSpectral simplicial complex

Identifiers

What OpenQuestion holds

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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.