Evidence map›Paper›PMID 30728826›Full record

ArticleFrontiers in genetics2018

Multiple Partial Regularized Nonnegative Matrix Factorization for Predicting Ontological Functions of lncRNAs.

Jianbang Zhao, Xiaoke Ma

Abstract read
In one paragraph

Article in Frontiers in genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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.

Jianbang ZhaoCollege of Information Engineering, Northwest Agriculture & Forestry University, Xianyang, China.
Xiaoke MaSchool of Computer Science and Technology, Xidian University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (LncRNA) are critical regulators for biological processes, which are highly related to complex diseases. Even though the next generation sequence technology facilitates the discovery of a great number of lncRNAs, the knowledge about the functions of lncRNAs is limited. Thus, it is promising to predict the functions of lncRNAs, which shed light on revealing the mechanisms of complex diseases. The current algorithms predict the functions of lncRNA by using the features of protein-coding genes. Generally speaking, these algorithms fuse heterogeneous genomic data to construct lncRNA-gene associations via a linear combination, which cannot fully characterize the function-lncRNA relations. To overcome this issue, we present an nonnegative matrix factorization algorithm with multiple partial regularization (aka MPrNMF) to predict the functions of lncRNAs without fusing the heterogeneous genomic data. In details, for each type of genomic data, we construct the lncRNA-gene associations, resulting in multiple associations. The proposed method integrates separately them via regularization strategy, rather than fuse them into a single type of associations. The results demonstrate that the proposed algorithm outperforms state-of-the-art methods based network-analysis. The model and algorithm provide an effective way to explore the functions of lncRNAs.

Indexed as

gene ontologylncRNAnetworksnonnegative matrix factorizationregularization

Identifiers

PMID30728826
PMCPMC6351489

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.