Evidence map›Paper›PMID 31881818›Full record

ArticleBMC bioinformatics2019

DeepMF: deciphering the latent patterns in omics profiles with a deep learning method.

Lingxi Chen, Jiao Xu, Shuai Cheng Li

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In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 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.

Lingxi ChenCity University of Hong Kong, 83 Tat Chee Ave, Kowloon Tong, Hong Kong, China.
Jiao XuCity University of Hong Kong, 83 Tat Chee Ave, Kowloon Tong, Hong Kong, China.
Shuai Cheng LiCity University of Hong Kong, 83 Tat Chee Ave, Kowloon Tong, Hong Kong, China. shuaicli@cityu.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith recent advances in high-throughput technologies, matrix factorization techniques are increasingly being utilized for mapping quantitative omics profiling matrix data into low-dimensional embedding space, in the hope of uncovering insights in the underlying biological processes. Nevertheless, current matrix factorization tools fall short in handling noisy data and missing entries, both deficiencies that are often found in real-life data.

resultsHere, we propose DeepMF, a deep neural network-based factorization model. DeepMF disentangles the association between molecular feature-associated and sample-associated latent matrices, and is tolerant to noisy and missing values. It exhibited feasible cancer subtype discovery efficacy on mRNA, miRNA, and protein profiles of medulloblastoma cancer, leukemia cancer, breast cancer, and small-blue-round-cell cancer, achieving the highest clustering accuracy of 76%, 100%, 92%, and 100% respectively. When analyzing data sets with 70% missing entries, DeepMF gave the best recovery capacity with silhouette values of 0.47, 0.6, 0.28, and 0.44, outperforming other state-of-the-art MF tools on the cancer data sets Medulloblastoma, Leukemia, TCGA BRCA, and SRBCT. Its embedding strength as measured by clustering accuracy is 88%, 100%, 84%, and 96% on these data sets, which improves on the current best methods 76%, 100%, 78%, and 87%.

conclusionDeepMF demonstrated robust denoising, imputation, and embedding ability. It offers insights to uncover the underlying biological processes such as cancer subtype discovery. Our implementation of DeepMF can be found at https://github.com/paprikachan/DeepMF.

Indexed as

Deep LearningGenomicsSoftwareAlgorithmsComputer SimulationDatabases, GeneticHumansMicroRNAsNeoplasmsNeural Networks, ComputerRNA, MessengerMicroRNAsRNA, MessengerCancer subtypeDeep learningDimension reductionMatrix factorizationOmics profile

Identifiers

PMID31881818
PMCPMC6933662

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LicenceCC BY
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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.