Evidence map›Paper›PMID 28950906›Full record

ArticleBMC systems biology2017

Mimvec: a deep learning approach for analyzing the human phenome.

Mingxin Gan, Wenran Li, Wanwen Zeng, Xiaojian Wang, Rui Jiang

Abstract read
In one paragraph

Article in BMC systems biology, 2017. 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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2 · The registry

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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.

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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

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5 · Who and what money

Authors and funding

5 authors.

Mingxin GanDepartment of Management Science and Engineering, Dongling School of Economics and Management, University of Science and Technology Beijing, Beijing, 100083, China.
Wenran LiMinistry of Education Key Laboratory of Bioinformatics; Bioinformatics Division, Department of Automation and Tsinghua National Laboratory for Information Science and Technology, Tsinghua University, Beijing, 100084, China.
Wanwen ZengMinistry of Education Key Laboratory of Bioinformatics; Bioinformatics Division, Department of Automation and Tsinghua National Laboratory for Information Science and Technology, Tsinghua University, Beijing, 100084, China.
Xiaojian WangState Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Rui JiangMinistry of Education Key Laboratory of Bioinformatics; Bioinformatics Division, Department of Automation and Tsinghua National Laboratory for Information Science and Technology, Tsinghua University, Beijing, 100084, China. ruijiang@tsinghua.edu.cn.

Funding

Selectively targeting delta opioid receptor subtypes to control drinking behaviorR01AA020401 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WHISTLER, JENNIFER L · 2011 to 2015
$1.8M
NIAAA NIH HHS R01 AA020401
6 · The paper itself

Abstract

backgroundThe human phenome has been widely used with a variety of genomic data sources in the inference of disease genes. However, most existing methods thus far derive phenotype similarity based on the analysis of biomedical databases by using the traditional term frequency-inverse document frequency (TF-IDF) formulation. This framework, though intuitive, not only ignores semantic relationships between words but also tends to produce high-dimensional vectors, and hence lacks the ability to precisely capture intrinsic semantic characteristics of biomedical documents. To overcome these limitations, we propose a framework called mimvec to analyze the human phenome by making use of the state-of-the-art deep learning technique in natural language processing.

resultsWe converted 24,061 records in the Online Mendelian Inheritance in Man (OMIM) database to low-dimensional vectors using our method. We demonstrated that the vector presentation not only effectively enabled classification of phenotype records against gene ones, but also succeeded in discriminating diseases of different inheritance styles and different mechanisms. We further derived pairwise phenotype similarities between 7988 human inherited diseases using their vector presentations. With a joint analysis of this phenome with multiple genomic data, we showed that phenotype overlap indeed implied genotype overlap. We finally used the derived phenotype similarities with genomic data to prioritize candidate genes and demonstrated advantages of this method over existing ones.

conclusionsOur method is capable of not only capturing semantic relationships between words in biomedical records but also alleviating the dimensional disaster accompanying the traditional TF-IDF framework. With the approaching of precision medicine, there will be abundant electronic records of medicine and health awaiting for deep analysis, and we expect to see a wide spectrum of applications borrowing the idea of our method in the near future.

Indexed as

Machine LearningPhenotypeComputational BiologyDatabases, GeneticDiseaseHumansInheritance PatternsNatural Language Processing

Identifiers

PMID28950906
PMCPMC5615244

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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.