常见疾病的表观基因组基础。
The epigenomic basis of common diseases.
作者信息
Rodger Euan J, Chatterjee Aniruddha
机构信息
Department of Pathology, Dunedin School of Medicine, University of Otago, Hanover Street, P.O. Box 56, Dunedin, 9054 New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, Level 2, 3A Symonds Street, Auckland, New Zealand.
出版信息
Clin Epigenetics. 2017 Jan 19;9:5. doi: 10.1186/s13148-017-0313-y. eCollection 2017.
Abstract
A report of the 6 Epigenomics of Common Diseases Conference held at the Wellcome Genome Campus in Hinxton, Cambridge, UK, on 1-4 November 2016.
摘要
2016年11月1日至4日在英国剑桥欣克斯顿惠康基因组校园举行的第六届常见疾病表观基因组学会议报告。
相似文献
1
The epigenomic basis of common diseases.常见疾病的表观基因组基础。
Clin Epigenetics. 2017 Jan 19;9:5. doi: 10.1186/s13148-017-0313-y. eCollection 2017.
2
Mapping human epigenomes.绘制人类表观基因组图谱。
Cell. 2013 Sep 26;155(1):39-55. doi: 10.1016/j.cell.2013.09.011.
3
Analyzing DNA Methylation Patterns During Tumor Evolution.分析肿瘤演化过程中的DNA甲基化模式。
Methods Mol Biol. 2018;1711:27-53. doi: 10.1007/978-1-4939-7493-1_3.
4
DNA immunoprecipitation semiconductor sequencing (DIP-SC-seq) as a rapid method to generate genome wide epigenetic signatures.DNA免疫沉淀半导体测序（DIP-SC-seq）作为一种生成全基因组表观遗传特征的快速方法。
Sci Rep. 2015 May 14;5:9778. doi: 10.1038/srep09778.
5
Bioinformatics Analysis of DNA Methylation Through Bisulfite Sequencing Data.基于亚硫酸氢盐测序数据的 DNA 甲基化的生物信息学分析。
Methods Mol Biol. 2021;2198:441-450. doi: 10.1007/978-1-0716-0876-0_32.
6
Preprocessing and Computational Analysis of Single-Cell Epigenomic Datasets.单细胞表观基因组数据集的预处理与计算分析
Methods Mol Biol. 2019;1935:187-202. doi: 10.1007/978-1-4939-9057-3_13.
7
Targeted bisulfite sequencing for biomarker discovery.靶向亚硫酸氢盐测序用于生物标志物发现。
Methods. 2021 Mar;187:13-27. doi: 10.1016/j.ymeth.2020.07.006. Epub 2020 Aug 2.
8
High-throughput approaches for plant epigenomic studies.高通量方法在植物表观基因组学研究中的应用。
Curr Opin Plant Biol. 2011 Apr;14(2):130-6. doi: 10.1016/j.pbi.2011.03.010. Epub 2011 Apr 4.
9
Whole-Genome Bisulfite Sequencing and Epigenetic Variation in Cereal Methylomes.谷物甲基化组中的全基因组亚硫酸氢盐测序与表观遗传变异
Methods Mol Biol. 2020;2072:119-128. doi: 10.1007/978-1-4939-9865-4_10.
10
Epigenomics: sequencing the methylome.表观基因组学：对甲基化组进行测序。
Methods Mol Biol. 2013;973:39-54. doi: 10.1007/978-1-62703-281-0_3.
引用本文的文献
1
Heavy Metals in Umbilical Cord Blood: Effects on Epigenetics and Child Development.脐带血中的重金属：对表观遗传学和儿童发育的影响。
Cells. 2024 Oct 26;13(21):1775. doi: 10.3390/cells13211775.
2
Precision medicine from a citizen perspective: a survey of public attitudes towards pharmacogenomics in Flanders.从公民角度看精准医学：弗拉芒公众对药物基因组学的态度调查。
BMC Med Genomics. 2022 Sep 12;15(Suppl 3):193. doi: 10.1186/s12920-022-01308-7.
3
DNA methylation changes in cord blood and the developmental origins of health and disease - a systematic review and replication study.脐带血中的 DNA 甲基化变化与健康和疾病的发育起源——系统评价和复制研究。
BMC Genomics. 2022 Mar 19;23(1):221. doi: 10.1186/s12864-022-08451-6.
4
Replication and expansion of epigenome-wide association literature in a black South African population.在南非黑人人群中复制和扩展表观基因组关联文献。
Clin Epigenetics. 2020 Jan 7;12(1):6. doi: 10.1186/s13148-019-0805-z.
本文引用的文献
1
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity.体重指数的全表观基因组关联研究以及肥胖的不良后果。
Nature. 2017 Jan 5;541(7635):81-86. doi: 10.1038/nature20784. Epub 2016 Dec 21.
2
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data.eFORGE：一种用于识别表观基因组数据中细胞类型特异性信号的工具。
Cell Rep. 2016 Nov 15;17(8):2137-2150. doi: 10.1016/j.celrep.2016.10.059.
3
CORALINA: a universal method for the generation of gRNA libraries for CRISPR-based screening.CORALINA：一种用于生成基于CRISPR筛选的gRNA文库的通用方法。
BMC Genomics. 2016 Nov 14;17(1):917. doi: 10.1186/s12864-016-3268-z.
4
Formation of new chromatin domains determines pathogenicity of genomic duplications.新染色质结构域的形成决定了基因组重复的致病性。
Nature. 2016 Oct 13;538(7624):265-269. doi: 10.1038/nature19800. Epub 2016 Oct 5.
5
Epigenetic profiling to classify cancer of unknown primary: a multicentre, retrospective analysis.基于表观遗传学特征对不明原发灶癌进行分类：一项多中心、回顾性分析。
Lancet Oncol. 2016 Oct;17(10):1386-1395. doi: 10.1016/S1470-2045(16)30297-2. Epub 2016 Aug 27.
6
A Landscape of Pharmacogenomic Interactions in Cancer.癌症中的药物基因组学相互作用全景
Cell. 2016 Jul 28;166(3):740-754. doi: 10.1016/j.cell.2016.06.017. Epub 2016 Jul 7.
7
Resolving early mesoderm diversification through single-cell expression profiling.通过单细胞表达谱分析解析早期中胚层分化
Nature. 2016 Jul 14;535(7611):289-293. doi: 10.1038/nature18633. Epub 2016 Jul 6.
8
Placental Hypomethylation Is More Pronounced in Genomic Loci Devoid of Retroelements.胎盘低甲基化在缺乏逆转录元件的基因组位点中更为明显。
G3 (Bethesda). 2016 Jul 7;6(7):1911-21. doi: 10.1534/g3.116.030379.
9
Genome-scale DNA methylome and transcriptome profiling of human neutrophils.人类中性粒细胞全基因组 DNA 甲基化组和转录组谱分析。
Sci Data. 2016 Mar 15;3:160019. doi: 10.1038/sdata.2016.19.
10
Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer.表观基因组分析检测到人类癌症中异常的超级增强子DNA甲基化。
Genome Biol. 2016 Jan 26;17:11. doi: 10.1186/s13059-016-0879-2.
Zotero 插件