Integration of evidence across human and model organism studies: A meeting report.
Integration of evidence across human and model organism studies: A meeting report.
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DOI:
10.1111/gbb.12738
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发表时间:
2021-04-23
期刊:
影响因子:
--
通讯作者:
Williams RW
中科院分区:
文献类型:
--
作者:
Palmer RHC;Johnson EC;Won H;Polimanti R;Kapoor M;Chitre A;Bogue MA;Benca-Bachman CE;Parker CC;Verma A;Reynolds T;Ernst J;Bray M;Kwon SB;Lai D;Quach BC;Gaddis NC;Saba L;Chen H;Hawrylycz M;Zhang S;Zhou Y;Mahaffey S;Fischer C;Sanchez-Roige S;Bandrowski A;Lu Q;Shen L;Philip V;Gelernter J;Bierut LJ;Hancock DB;Edenberg HJ;Johnson EO;Nestler EJ;Barr PB;Prins P;Smith DJ;Akbarian S;Thorgeirsson T;Walton D;Baker E;Jacobson D;Palmer AA;Miles M;Chesler EJ;Emerson J;Agrawal A;Martone M;Williams RW
The National Institute on Drug Abuse and Joint Institute for Biological Sciences at the Oak Ridge National Laboratory hosted a meeting attended by a diverse group of scientists with expertise in substance use disorders (SUDs), computational biology, and FAIR (Findability, Accessibility, Interoperability, and Reusability) data sharing. The meeting's objective was to discuss and evaluate better strategies to integrate genetic, epigenetic, and 'omics data across human and model organisms to achieve deeper mechanistic insight into SUDs. Specific topics were to (a) evaluate the current state of substance use genetics and genomics research and fundamental gaps, (b) identify opportunities and challenges of integration and sharing across species and data types, (c) identify current tools and resources for integration of genetic, epigenetic, and phenotypic data, (d) discuss steps and impediment related to data integration, and (e) outline future steps to support more effective collaboration—particularly between animal model research communities and human genetics and clinical research teams. This review summarizes key facets of this catalytic discussion with a focus on new opportunities and gaps in resources and knowledge on SUDs. This report discusses gaps in knowledge and possibilities for the next phase of functional discovery for addiction.
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影响因子:
14.9
作者:
Baker EJ;Jay JJ;Bubier JA;Langston MA;Chesler EJ
通讯作者:
Chesler EJ
影响因子:
2.5
作者:
Churchill, Gary A.;Gatti, Daniel M.;Munger, Steven C.;Svenson, Karen L.
通讯作者:
Svenson, Karen L.
DOI:
10.1126/science.aaf5098
发表时间:
2016-10-07
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Fan S;Hansen ME;Lo Y;Tishkoff SA
通讯作者:
Tishkoff SA
影响因子:
11
作者:
Buchwald, Jadwiga;Chenoweth, Meghan J.;Tyndale, Rachel F.
通讯作者:
Tyndale, Rachel F.
影响因子:
11
作者:
Byrne EM;Zhu Z;Qi T;Skene NG;Bryois J;Pardinas AF;Stahl E;Smoller JW;Rietschel M;Bipolar Working Group of the Psychiatric Genomics Consortium;Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium;Owen MJ;Walters JTR;O'Donovan MC;McGrath JG;Hjerling-Leffler J;Sullivan PF;Goddard ME;Visscher PM;Yang J;Wray NR
通讯作者:
Wray NR