Machine Learning Advanced Dynamic Omics Data Analysis for Precision Medicine (Record no. 63282)

MARC details
000 -LEADER
fixed length control field 03869naaaa2200409uu 4500
001 - CONTROL NUMBER
control field https://directory.doabooks.org/handle/20.500.12854/73706
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220220034818.0
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 978-2-88963-554-2
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9782889635542
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3389/978-2-88963-554-2
Terms of availability doi
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title English
042 ## - AUTHENTICATION CODE
Authentication code dc
072 #7 - SUBJECT CATEGORY CODE
Subject category code PD
Source bicssc
072 #7 - SUBJECT CATEGORY CODE
Subject category code MFN
Source bicssc
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Zeng, Tao
Relationship edt
245 10 - TITLE STATEMENT
Title Machine Learning Advanced Dynamic Omics Data Analysis for Precision Medicine
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Frontiers Media SA
Date of publication, distribution, etc. 2020
300 ## - PHYSICAL DESCRIPTION
Extent 1 electronic resource (393 p.)
506 0# - RESTRICTIONS ON ACCESS NOTE
Terms governing access Open Access
Source of term star
Standardized terminology for access restriction Unrestricted online access
520 ## - SUMMARY, ETC.
Summary, etc. Precision medicine is being developed as a preventative, diagnostic and treatment tool to combat complex human diseases in a personalized manner. By utilizing high-throughput technologies, dynamic ‘omics data including genetics, epi-genetics and even meta-genomics has produced temporal-spatial big biological datasets which can be associated with individual genotypes underlying pathogen progressive phenotypes. It is therefore necessary to investigate how to integrate these multi-scale ‘omics datasets to distinguish the novel individual-specific disease causes from conventional cohort-common disease causes. Currently, machine learning plays an important role in biological and biomedical research, especially in the analysis of big ‘omics data. However, in contrast to traditional big social data, ‘omics datasets are currently always “small-sample-high-dimension”, which causes overwhelming application problems and also introduces new challenges: (1) Big ‘omics datasets can be extremely unbalanced, due to the difficulty of obtaining enough positive samples of such rare mutations or rare diseases; (2) A large number of machine learning models are “black box,” which is enough to apply in social applications. However, in biological or biomedical fields, knowledge of the molecular mechanisms underlying any disease or biological study is necessary to deepen our understanding; (3) The genotype-phenotype association is a “white clue” captured in conventional big data studies. But identification of “causality” rather than association would be more helpful for physicians or biologists, as this can be used to determine an experimental target as the subject of future research. Therefore, to simultaneously improve the phenotype discrimination and genotype interpretability for complex diseases, it is necessary: To design and implement new machine learning technologies to integrate prior-knowledge with new ‘omics datasets to provide transferable learning methods by combining multiple sources of data; To develop new network-based theories and methods to balance the trade-off between accuracy and interpretability of machine learning in biomedical and biological domains; To enhance the causality inference on “small-sample high dimension” data to capture the personalized causal relationship.
540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE
Terms governing use and reproduction Creative Commons
Use and reproduction rights https://creativecommons.org/licenses/by/4.0/
Source of term cc
-- https://creativecommons.org/licenses/by/4.0/
546 ## - LANGUAGE NOTE
Language note English
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Science: general issues
Source of heading or term bicssc
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medical genetics
Source of heading or term bicssc
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term machine learning
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term dynamic
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term OMICS data
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term precision medicine
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term integration
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Huang, Tao
Relationship edt
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lu, Chuan
Relationship edt
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Zeng, Tao
Relationship oth
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Huang, Tao
Relationship oth
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lu, Chuan
Relationship oth
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://www.frontiersin.org/research-topics/8239/machine-learning-advanced-dynamic-omics-data-analysis-for-precision-medicine#articles">https://www.frontiersin.org/research-topics/8239/machine-learning-advanced-dynamic-omics-data-analysis-for-precision-medicine#articles</a>
Access status 0
Public note DOAB: download the publication
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://directory.doabooks.org/handle/20.500.12854/73706">https://directory.doabooks.org/handle/20.500.12854/73706</a>
Access status 0
Public note DOAB: description of the publication

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