Medical and Regulatory Genomics
Medical and Regulatory Genomics
批准号:
MC_UU_00007/16
负责人:
Colin Semple
金额:
$190.62万
依托单位:
依托单位国家:
英国
项目类别:
Intramural
财政年份:
2018
资助国家:
英国
项目状态:
已结题
起止时间:
2018 至 --
中文摘要
你的基因组中嵌入的基因具有复杂的活动模式,特定的基因星座必须在特定的细胞和特定的时间活跃,才能成功完成生物过程,如胚胎发育。我们小组对基因调控的基本生物学感兴趣:基因何时、如何以及为什么被开启和关闭。我们通过对测量数千个基因活性的数据集的计算分析,促进了对基因调控潜在机制的理解。这可以为人类进化本身提供新的见解,也有助于我们解释调控中断的疾病过程,如癌症和发育障碍。人类基因组在不同个体之间存在数百万个DNA位点的差异,但我们通常不知道哪些变异对我们的生物学最重要。最终,我们希望基于我们对基因调控的了解,开发预测模型,帮助我们预测变异对健康和疾病的影响。
英文摘要
The genes embedded in your genome have complex patterns of activity and particular constellations of genes must be active in particular cells and at particular times for biological processes, such as embryonic development, to conclude successfully. Our group is interested in the fundamental biology of gene regulation: when, how and why genes are turned on and off. We advance understand of the mechanisms underlying gene regulation, using computational analyses of datasets measuring the activities of many thousands of genes. This can provide new insights into human evolution itself, and also helps us to interpret disease processes with disrupted regulation, such as cancers and developmental disorders. Human genomes vary at millions of DNA sites between individuals, but often we do not know which variants matter most to our biology. Ultimately we want to develop predictive models, based upon our knowledge of gene regulation, that help us to forecast the effects of variants in health and disease.
期刊论文(10)
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会议论文
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DOI:
10.1186/s13059-019-1635-1
发表时间:
2019-02-08
期刊:
GENOME BIOLOGY
影响因子:
12.3
作者:
[Ballinger, Tracy J., Bouwman, Britta A. M., Semple, Colin A.]
通讯作者:
Semple, Colin A.
DOI:
10.1038/s41398-021-01256-3
发表时间:
2021-02-19
期刊:
Translational psychiatry
影响因子:
6.8
作者:
[Bonneau M, Sullivan STO, Gonzalez-Lozano MA, Baxter P, Gautier P, Marchisella E, Hardingham NR, Chesters RA, Torrance H, Howard DM, Jansen MA, McMillan M, Singh Y, Didier M, Koopmans F, Semple CA, McIntosh AM, Volkmer H, Loos M, Fox K, Hardingham GE, Vernon AC, Porteous DJ, Smit AB, Price DJ, Kirsty Millar J]
通讯作者:
Kirsty Millar J
DOI:
10.1038/s41586-020-2435-1
发表时间:
2020-07-01
期刊:
Nature
影响因子:
64.8
作者:
[Aitken, Sarah J, Anderson, Craig J, Taylor, Martin S]
通讯作者:
Taylor, Martin S
IMPROVE-DD: Integrating Multiple Phenotype Resources Optimises Variant Evaluation in genetically determined Developmental Disorders
IMPROVE-DD:整合多种表型资源优化遗传决定的发育障碍的变异评估
DOI:
10.1101/2022.05.20.22275135
发表时间:
2022
期刊:
影响因子:
--
作者:
[Aitken S]
通讯作者:
Aitken S
DOI:
10.12688/f1000research.16079.1
发表时间:
2018-01-01
期刊:
F1000Research
影响因子:
--
作者:
[Ewing, Ailith, Semple, Colin]
通讯作者:
Semple, Colin
共 8 条
Origins and impacts of regulatory mutations
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批准号:MC_UU_00035/1
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项目类别:Intramural
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资助金额:$307.59万
-
财政年份:2023
-
负责人:Colin Semple
-
依托单位:
国内基金
海外基金
慢性乙肝感染中枯否细胞(KC)诱导肝内自然杀伤细胞(NK)向免疫调节功能(regulatory NK)倾斜的机制及在肝纤维化中的作用
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批准号:81970529
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项目类别:面上项目
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资助金额:57.0万元
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批准年份:2019
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负责人:李海军
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依托单位:
APO-miR(multi-targeting apoptosis-regulatory miRNA)在前列腺癌中的表达和作用
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批准号:81101529
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项目类别:青年科学基金项目
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资助金额:22.0万元
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批准年份:2011
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负责人:陈雪芹
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依托单位: