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COGA 协作研究以及遗传分析工作坊 14 的单核苷酸多态性基因分型的数据描述。

Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14.

机构信息

Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN, USA.

出版信息

BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S2. doi: 10.1186/1471-2156-6-S1-S2.

DOI:10.1186/1471-2156-6-S1-S2
PMID:16451628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1866767/
Abstract

The data provided to the Genetic Analysis Workshop 14 (GAW 14) was the result of a collaboration among several different groups, catalyzed by Elizabeth Pugh from The Center for Inherited Disease Research (CIDR) and the organizers of GAW 14, Jean MacCluer and Laura Almasy. The DNA, phenotypic characterization, and microsatellite genomic survey were provided by the Collaborative Study on the Genetics of Alcoholism (COGA), a nine-site national collaboration funded by the National Institute of Alcohol and Alcoholism (NIAAA) and the National Institute of Drug Abuse (NIDA) with the overarching goal of identifying and characterizing genes that affect the susceptibility to develop alcohol dependence and related phenotypes. CIDR, Affymetrix, and Illumina provided single-nucleotide polymorphism genotyping of a large subset of the COGA subjects. This article briefly describes the dataset that was provided.

摘要

提供给遗传分析工作坊 14(GAW 14)的数据是由多个不同小组合作的结果,由伊丽莎白·普格(Elizabeth Pugh)从遗传性疾病研究中心(CIDR)以及 GAW 14 的组织者吉恩·麦克卢尔(Jean MacCluer)和劳拉·阿玛西(Laura Almasy)推动。DNA、表型特征和微卫星基因组调查由酒精中毒遗传学合作研究(COGA)提供,这是一个由国家酒精滥用与酒精中毒研究所(NIAAA)和国家药物滥用研究所(NIDA)资助的九个地点的全国性合作,其总体目标是确定和描述影响易感性的基因,从而导致酒精依赖和相关表型。CIDR、Affymetrix 和 Illumina 为 COGA 的大部分受试者提供了单核苷酸多态性基因分型。本文简要描述了提供的数据集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a9/1866767/94ff84432254/1471-2156-6-S1-S2-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a9/1866767/94ff84432254/1471-2156-6-S1-S2-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a9/1866767/94ff84432254/1471-2156-6-S1-S2-1.jpg

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本文引用的文献

1
The Collaborative Study on the Genetics of Alcoholism.酒精中毒遗传学合作研究
Alcohol Health Res World. 1995;19(3):228-236.
2
The genetics of oscillations in the human brain.人类大脑振荡的遗传学
Suppl Clin Neurophysiol. 2004;57:441-9. doi: 10.1016/s1567-424x(09)70382-4.
3
A highly informative SNP linkage panel for human genetic studies.用于人类遗传学研究的高信息量单核苷酸多态性(SNP)连锁图谱。
狂饮和高度饮酒——与静脉内酒精自我给药和潜在风险因素的关联。
Addict Biol. 2022;27(6):e13228. doi: 10.1111/adb.13228.
4
Genome-wide association study of stimulant dependence.兴奋剂依赖的全基因组关联研究。
Transl Psychiatry. 2021 Jun 29;11(1):363. doi: 10.1038/s41398-021-01440-5.
5
Predicting alcohol use disorder remission: a longitudinal multimodal multi-featured machine learning approach.预测酒精使用障碍缓解:一种纵向多模态多特征机器学习方法。
Transl Psychiatry. 2021 Mar 15;11(1):166. doi: 10.1038/s41398-021-01281-2.
6
Predicting risk for Alcohol Use Disorder using longitudinal data with multimodal biomarkers and family history: a machine learning study.利用具有多模态生物标志物和家族史的纵向数据预测酒精使用障碍风险:一项机器学习研究。
Mol Psychiatry. 2021 Apr;26(4):1133-1141. doi: 10.1038/s41380-019-0534-x. Epub 2019 Oct 8.
7
Neurexin 3 transmembrane and soluble isoform expression and splicing haplotype are associated with neuron inflammasome and Alzheimer's disease.神经连接蛋白 3 跨膜和可溶性同种型表达和剪接单体型与神经元炎症小体和阿尔茨海默病有关。
Alzheimers Res Ther. 2019 Mar 21;11(1):28. doi: 10.1186/s13195-019-0475-2.
8
Using an Event-History with Risk-Free Model to Study the Genetics of Alcoholism.使用无风险模型的事件史研究酒精中毒的遗传学。
Sci Rep. 2017 May 16;7(1):1975. doi: 10.1038/s41598-017-01791-4.
9
Ventral striatal regulation of CREM mediates impulsive action and drug addiction vulnerability.腹侧纹状体调节 CREM 介导冲动行为和药物成瘾易感性。
Mol Psychiatry. 2018 May;23(5):1328-1335. doi: 10.1038/mp.2017.80. Epub 2017 Apr 25.
10
Single Nucleotide Polymorphism Associated with Altered Brain Responses (but not Performance) during Measures of Impulsivity and Reward Sensitivity in Human Adolescents.与人类青少年冲动性和奖励敏感性测量期间大脑反应改变(而非行为表现)相关的单核苷酸多态性
Front Behav Neurosci. 2017 Feb 15;11:24. doi: 10.3389/fnbeh.2017.00024. eCollection 2017.
Nat Methods. 2004 Nov;1(2):113-7. doi: 10.1038/nmeth712. Epub 2004 Oct 21.
4
Highly parallel SNP genotyping.高度并行单核苷酸多态性基因分型
Cold Spring Harb Symp Quant Biol. 2003;68:69-78. doi: 10.1101/sqb.2003.68.69.
5
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Hum Mol Genet. 2004 Sep 1;13(17):1903-11. doi: 10.1093/hmg/ddh194. Epub 2004 Jun 30.
6
Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition.诱发脑电图振荡与CHRM2受体基因多态性的连锁及连锁不平衡:对人类脑动力学和认知的影响
Int J Psychophysiol. 2004 Jul;53(2):75-90. doi: 10.1016/j.ijpsycho.2004.02.004.
7
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8
Decoding randomly ordered DNA arrays.解码随机排序的DNA阵列。
Genome Res. 2004 May;14(5):870-7. doi: 10.1101/gr.2255804. Epub 2004 Apr 12.
9
Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations.编码γ-氨基丁酸A(GABA(A))受体α2亚基的GABRA2基因变异与酒精依赖及脑电波振荡有关。
Am J Hum Genet. 2004 Apr;74(4):705-14. doi: 10.1086/383283. Epub 2004 Mar 12.
10
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array.使用单引物分析在高密度寡核苷酸阵列上对超过10,000个单核苷酸多态性进行平行基因分型。
Genome Res. 2004 Mar;14(3):414-25. doi: 10.1101/gr.2014904.