• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
A knowledge base for tracking the impact of genomics on population health.一个用于追踪基因组学对人群健康影响的知识库。
Genet Med. 2016 Dec;18(12):1312-1314. doi: 10.1038/gim.2016.63. Epub 2016 Jun 9.
2
HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders.HLBS-PopOmics:一个在线知识库,旨在加速人群基因组学研究进展的传播和实施,以减轻心脏、肺部、血液和睡眠障碍的负担。
Genet Med. 2019 Mar;21(3):519-524. doi: 10.1038/s41436-018-0118-1. Epub 2018 Sep 10.
3
COVID-19 GPH: tracking the contribution of genomics and precision health to the COVID-19 pandemic response.COVID-19 GPH:追踪基因组学和精准健康对 COVID-19 大流行应对的贡献。
BMC Infect Dis. 2022 Apr 25;22(1):402. doi: 10.1186/s12879-022-07219-3.
4
Lynx: a database and knowledge extraction engine for integrative medicine.灵奇:一个用于整合医学的数据库和知识提取引擎。
Nucleic Acids Res. 2014 Jan;42(Database issue):D1007-12. doi: 10.1093/nar/gkt1166. Epub 2013 Nov 21.
5
GGDonto ontology as a knowledge-base for genetic diseases and disorders of glycan metabolism and their causative genes.GGDonto本体作为遗传疾病和聚糖代谢紊乱及其致病基因的知识库。
J Biomed Semantics. 2018 Apr 18;9(1):14. doi: 10.1186/s13326-018-0182-0.
6
PharmGKB: the Pharmacogenomics Knowledge Base.药物基因组学知识库(PharmGKB)
Methods Mol Biol. 2013;1015:311-20. doi: 10.1007/978-1-62703-435-7_20.
7
CGKB: an annotation knowledge base for cowpea (Vigna unguiculata L.) methylation filtered genomic genespace sequences.CGKB:豇豆(Vigna unguiculata L.)甲基化过滤基因组基因空间序列的注释知识库。
BMC Bioinformatics. 2007 Apr 19;8:129. doi: 10.1186/1471-2105-8-129.
8
Scaling up data curation using deep learning: An application to literature triage in genomic variation resources.利用深度学习扩展数据管理:在基因组变异资源文献分类中的应用。
PLoS Comput Biol. 2018 Aug 13;14(8):e1006390. doi: 10.1371/journal.pcbi.1006390. eCollection 2018 Aug.
9
COSMIC: a curated database of somatic variants and clinical data for cancer.COSMIC:一个针对癌症体细胞变异和临床数据的精选数据库。
Nucleic Acids Res. 2024 Jan 5;52(D1):D1210-D1217. doi: 10.1093/nar/gkad986.
10
Knowledge Base Commons (KBCommons) v1.1: a universal framework for multi-omics data integration and biological discoveries.知识库共通体(KBCommons)v1.1:一种用于多组学数据集成和生物学发现的通用框架。
BMC Genomics. 2019 Dec 20;20(Suppl 11):947. doi: 10.1186/s12864-019-6287-8.

引用本文的文献

1
A landscape of gene expression regulation for synovium in arthritis.关节炎滑膜基因表达调控的全景图。
Nat Commun. 2024 Feb 15;15(1):1409. doi: 10.1038/s41467-024-45652-x.
2
Clocking Epilepsies: A Chronomodulated Strategy-Based Therapy for Rhythmic Seizures.致癫时钟:节律性癫痫的一种基于时间调控策略的治疗方法。
Int J Mol Sci. 2023 Feb 20;24(4):4223. doi: 10.3390/ijms24044223.
3
Risk-Adjusted Cancer Screening and Prevention (RiskAP): Complementing Screening for Early Disease Detection by a Learning Screening Based on Risk Factors.风险调整后的癌症筛查与预防(RiskAP):通过基于风险因素的学习型筛查补充早期疾病检测筛查
Breast Care (Basel). 2022 Apr;17(2):208-223. doi: 10.1159/000517182. Epub 2021 Aug 12.
4
The Mechanism of as a Treatment for Hyperlipidemia Based on Network Pharmacology and Experimental Validation.基于网络药理学和实验验证的[药物名称]治疗高脂血症的机制
Evid Based Complement Alternat Med. 2022 Apr 13;2022:5821829. doi: 10.1155/2022/5821829. eCollection 2022.
5
COVID-19 GPH: tracking the contribution of genomics and precision health to the COVID-19 pandemic response.COVID-19 GPH:追踪基因组学和精准健康对 COVID-19 大流行应对的贡献。
BMC Infect Dis. 2022 Apr 25;22(1):402. doi: 10.1186/s12879-022-07219-3.
6
Impact of BMI and waist circumference on epigenome-wide DNA methylation and identification of epigenetic biomarkers in blood: an EWAS in multi-ethnic Asian individuals.体重指数和腰围对全基因组 DNA 甲基化的影响及血液表观遗传生物标志物的鉴定:多民族亚洲人群的 EWAS 研究。
Clin Epigenetics. 2021 Oct 20;13(1):195. doi: 10.1186/s13148-021-01162-x.
7
From Patient Engagement to Precision Oncology: Leveraging Informatics to Advance Cancer Care.从患者参与到精准肿瘤学:利用信息学推进癌症护理。
Yearb Med Inform. 2020 Aug;29(1):235-242. doi: 10.1055/s-0040-1701983. Epub 2020 Aug 21.
8
Tracking human genes along the translational continuum.追踪人类基因在翻译连续体中的情况。
NPJ Genom Med. 2019 Oct 16;4:25. doi: 10.1038/s41525-019-0100-0. eCollection 2019.
9
First Responder to Genomic Information: A Guide for Primary Care Providers.基因组信息的第一响应者:初级保健提供者指南。
Mol Diagn Ther. 2019 Aug;23(4):459-466. doi: 10.1007/s40291-019-00407-z.
10
Using deep learning to identify translational research in genomic medicine beyond bench to bedside.利用深度学习技术识别基因组医学领域中从基础研究到临床应用的转化研究。
Database (Oxford). 2019 Jan 1;2019:baz010. doi: 10.1093/database/baz010.

本文引用的文献

1
Horizon scanning for translational genomic research beyond bench to bedside.超越从实验室到临床的转化基因组研究的前沿领域扫描。
Genet Med. 2014 Jul;16(7):535-8. doi: 10.1038/gim.2013.184. Epub 2014 Jan 9.
2
Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.按证据水平优先考虑基因组应用的行动:一种 horizon-scanning 方法。
Clin Pharmacol Ther. 2014 Apr;95(4):394-402. doi: 10.1038/clpt.2013.226. Epub 2014 Feb 19.
3
Charting a course for genomic medicine from base pairs to bedside.为基因组医学绘制从碱基对到床边的路线图。
Nature. 2011 Feb 10;470(7333):204-13. doi: 10.1038/nature09764.
4
The genomic applications in practice and prevention network.基因组学在实践与预防方面的应用网络。
Genet Med. 2009 Jul;11(7):488-94. doi: 10.1097/GIM.0b013e3181a551cc.
5
GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique.GAP筛选器:一种利用支持向量机技术在PubMed中筛选人类基因关联文献的自动工具。
BMC Bioinformatics. 2008 Apr 22;9:205. doi: 10.1186/1471-2105-9-205.
6
A navigator for human genome epidemiology.人类基因组流行病学导航工具。
Nat Genet. 2008 Feb;40(2):124-5. doi: 10.1038/ng0208-124.
7
The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?基因组医学中的翻译研究连续统一体:我们如何加速将人类基因组发现合理整合到医疗保健和疾病预防中?
Genet Med. 2007 Oct;9(10):665-74. doi: 10.1097/GIM.0b013e31815699d0.

一个用于追踪基因组学对人群健康影响的知识库。

A knowledge base for tracking the impact of genomics on population health.

作者信息

Yu Wei, Gwinn Marta, Dotson W David, Green Ridgely Fisk, Clyne Mindy, Wulf Anja, Bowen Scott, Kolor Katherine, Khoury Muin J

机构信息

Office of Public Health Genomics, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

McKing Consulting Corporation, Atlanta, Georgia, USA.

出版信息

Genet Med. 2016 Dec;18(12):1312-1314. doi: 10.1038/gim.2016.63. Epub 2016 Jun 9.

DOI:10.1038/gim.2016.63
PMID:27280867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5133140/
Abstract

PURPOSE

We created an online knowledge base (the Public Health Genomics Knowledge Base (PHGKB)) to provide systematically curated and updated information that bridges population-based research on genomics with clinical and public health applications.

METHODS

Weekly horizon scanning of a wide variety of online resources is used to retrieve relevant scientific publications, guidelines, and commentaries. After curation by domain experts, links are deposited into Web-based databases.

RESULTS

PHGKB currently consists of nine component databases. Users can search the entire knowledge base or search one or more component databases directly and choose options for customizing the display of their search results.

CONCLUSION

PHGKB offers researchers, policy makers, practitioners, and the general public a way to find information they need to understand the complicated landscape of genomics and population health.Genet Med 18 12, 1312-1314.

摘要

目的

我们创建了一个在线知识库(公共卫生基因组学知识库(PHGKB)),以提供经过系统整理和更新的信息,搭建基于人群的基因组学研究与临床及公共卫生应用之间的桥梁。

方法

通过每周对各种在线资源进行前沿扫描,检索相关科学出版物、指南和评论。经领域专家整理后,链接被存入基于网络的数据库。

结果

PHGKB目前由九个组件数据库组成。用户可以搜索整个知识库,或直接搜索一个或多个组件数据库,并选择自定义搜索结果显示的选项。

结论

PHGKB为研究人员、政策制定者、从业者和普通公众提供了一种途径,以找到他们理解基因组学和人群健康复杂领域所需的信息。《遗传医学》18卷12期,1312 - 1314页。