• 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

otargen:基于 GraphQL 的 R 包,用于从 Open Targets Genetics 中获取和处理整洁数据。

otargen: GraphQL-based R package for tidy data accessing and processing from Open Targets Genetics.

机构信息

Bioinformatics Department, OMass Therapeutics, Oxford Business Park, ARC, Oxford OX4 2GX, United Kingdom.

出版信息

Bioinformatics. 2023 Aug 1;39(8). doi: 10.1093/bioinformatics/btad441.

DOI:10.1093/bioinformatics/btad441
PMID:37467069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10394122/
Abstract

MOTIVATION

Open Target Genetics is a comprehensive resource portal that offers variant-centric statistical evidence, enabling the prioritization of causal variants and the identification of potential drug targets. The portal uses GraphQL technology for efficient data query and provides endpoints for programmatic access for R and Python users. However, leveraging GraphQL for data retrieval can be challenging, time-consuming, and repetitive, requiring familiarity with the GraphQL query language and processing outputs in nested JSON (JavaScript Object Notation) format into tidy data tables. Therefore, developing open-source tools are required to simplify data retrieval processes to integrate valuable genetic information into data-driven target discovery pipelines seamlessly.

RESULTS

otargen is an open-source R package designed to make data retrieval and analysis from the Open Target Genetics portal as simple as possible for R users. The package offers a suite of functions covering all query types, allowing streamlined data access in a tidy table format. By executing only a single line of code, the otargen users avoid the repetitive scripting of complex GraphQL queries, including the post-processing steps. In addition, otargen contains convenient plotting functions to visualize and gain insights from complex data tables returned by several key functions.

AVAILABILITY AND IMPLEMENTATION

otargen is available at https://amirfeizi.github.io/otargen/.

摘要

动机

Open Target Genetics 是一个综合性的资源门户,提供以变体为中心的统计证据,用于优先考虑因果变体,并确定潜在的药物靶点。该门户使用 GraphQL 技术进行高效的数据查询,并为 R 和 Python 用户提供了程序化访问的端点。然而,利用 GraphQL 进行数据检索可能具有挑战性、耗时且重复,需要熟悉 GraphQL 查询语言,并将嵌套的 JSON(JavaScript 对象表示法)格式的处理输出转换为整洁的数据表。因此,需要开发开源工具来简化数据检索过程,以便将有价值的遗传信息无缝集成到数据驱动的目标发现管道中。

结果

otargen 是一个开源的 R 包,旨在为 R 用户尽可能简化从 Open Target Genetics 门户检索和分析数据的过程。该包提供了一系列涵盖所有查询类型的功能,允许以整洁的表格格式进行流线型的数据访问。通过仅执行一行代码,otargen 用户可以避免重复编写复杂的 GraphQL 查询及其后处理步骤。此外,otargen 包含方便的绘图功能,可用于可视化和从几个关键功能返回的复杂数据表中获取见解。

可用性和实现

otargen 可在 https://amirfeizi.github.io/otargen/ 获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c96/10394122/5a8d6d275634/btad441f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c96/10394122/5a8d6d275634/btad441f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c96/10394122/5a8d6d275634/btad441f1.jpg

相似文献

1
otargen: GraphQL-based R package for tidy data accessing and processing from Open Targets Genetics.otargen:基于 GraphQL 的 R 包,用于从 Open Targets Genetics 中获取和处理整洁数据。
Bioinformatics. 2023 Aug 1;39(8). doi: 10.1093/bioinformatics/btad441.
2
quincunx: an R package to query, download and wrangle PGS Catalog data.quincunx:一个用于查询、下载和整理 PGS Catalog 数据的 R 包。
Bioinformatics. 2021 Dec 22;38(1):294-296. doi: 10.1093/bioinformatics/btab522.
3
A fast and efficient python library for interfacing with the Biological Magnetic Resonance Data Bank.一个用于与生物磁共振数据库接口的快速高效的Python库。
BMC Bioinformatics. 2017 Mar 17;18(1):175. doi: 10.1186/s12859-017-1580-5.
4
NeuroPycon: An open-source python toolbox for fast multi-modal and reproducible brain connectivity pipelines.NeuroPycon:一个开源的 Python 工具包,用于快速进行多模态和可重复的脑连接管道。
Neuroimage. 2020 Oct 1;219:117020. doi: 10.1016/j.neuroimage.2020.117020. Epub 2020 Jun 6.
5
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.开放靶点遗传学:利用大规模遗传学和功能基因组学系统地识别与性状相关的基因。
Nucleic Acids Res. 2021 Jan 8;49(D1):D1311-D1320. doi: 10.1093/nar/gkaa840.
6
GraphQL for the delivery of bioinformatics web APIs and application to ZincBind.用于生物信息学网络应用程序编程接口交付及应用于锌结合的GraphQL
Bioinform Adv. 2021 Sep 29;1(1):vbab023. doi: 10.1093/bioadv/vbab023. eCollection 2021.
7
PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources.PyCellBase,一个高效的 Python 包,用于轻松从异构数据源中检索生物数据。
BMC Bioinformatics. 2019 Mar 28;20(1):159. doi: 10.1186/s12859-019-2726-4.
8
QLMDR: a GraphQL query language for ISO 11179-based metadata repositories.QLMDR:基于 ISO 11179 的元数据存储库的 GraphQL 查询语言。
BMC Med Inform Decis Mak. 2019 Mar 18;19(1):45. doi: 10.1186/s12911-019-0794-z.
9
BiocPkgTools: Toolkit for mining the package ecosystem.BiocPkgTools:用于挖掘软件包生态系统的工具包。
F1000Res. 2019 May 29;8:752. doi: 10.12688/f1000research.19410.1. eCollection 2019.
10
ExMove: An open-source toolkit for processing and exploring animal-tracking data in R.ExMove:一个用于在 R 中处理和探索动物追踪数据的开源工具包。
J Anim Ecol. 2024 Jul;93(7):784-795. doi: 10.1111/1365-2656.14111. Epub 2024 Jun 11.

引用本文的文献

1
Impact of genetic variants linked to liver fat and liver volume on MRI-mapped body composition.与肝脏脂肪和肝脏体积相关的基因变异对MRI映射的身体成分的影响。
JHEP Rep. 2025 Jun 2;7(9):101468. doi: 10.1016/j.jhepr.2025.101468. eCollection 2025 Sep.
2
Insulin- and exercise-induced phosphoproteomics of human skeletal muscle identify REPS1 as a regulator of muscle glucose uptake.胰岛素和运动诱导的人体骨骼肌磷酸化蛋白质组学研究确定REPS1为肌肉葡萄糖摄取的调节因子。
Cell Rep Med. 2025 Jun 17;6(6):102163. doi: 10.1016/j.xcrm.2025.102163. Epub 2025 Jun 6.
3
Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline.

本文引用的文献

1
FinnGen provides genetic insights from a well-phenotyped isolated population.FinnGen 为一个表型良好的隔离人群提供了遗传学方面的见解。
Nature. 2023 Jan;613(7944):508-518. doi: 10.1038/s41586-022-05473-8. Epub 2023 Jan 18.
2
The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.下一代开放靶点平台:重新构想、重新设计、重新构建。
Nucleic Acids Res. 2023 Jan 6;51(D1):D1353-D1359. doi: 10.1093/nar/gkac1046.
3
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.
结合横断面和纵向基因组学方法来确定认知和身体衰退的决定因素。
Nat Commun. 2025 May 15;16(1):4524. doi: 10.1038/s41467-025-59383-0.
4
Genetic factors shaping the plasma lipidome and the relations to cardiometabolic risk in children and adolescents.影响儿童和青少年血浆脂质组的遗传因素及其与心脏代谢风险的关系。
EBioMedicine. 2025 Feb;112:105537. doi: 10.1016/j.ebiom.2024.105537. Epub 2025 Jan 2.
5
Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery.开放靶点平台:助力药物研发中的治疗假说构建
Nucleic Acids Res. 2025 Jan 6;53(D1):D1467-D1475. doi: 10.1093/nar/gkae1128.
6
A Genome-Wide Association Study Suggests New Susceptibility Loci for Primary Antiphospholipid Syndrome.一项全基因组关联研究提示原发性抗磷脂综合征的新易感位点。
Arthritis Rheumatol. 2024 Nov;76(11):1623-1634. doi: 10.1002/art.42947. Epub 2024 Aug 11.
7
Kidney Volume and Risk of Incident Kidney Outcomes.肾脏体积与新发肾脏疾病结局风险
J Am Soc Nephrol. 2024 Jun 10;35(9):1240-51. doi: 10.1681/ASN.0000000000000419.
系统地优先考虑所有已发表的人类 GWAS 性状关联基因座的因果变异和基因的开放方法。
Nat Genet. 2021 Nov;53(11):1527-1533. doi: 10.1038/s41588-021-00945-5. Epub 2021 Oct 28.
4
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.开放靶点遗传学:利用大规模遗传学和功能基因组学系统地识别与性状相关的基因。
Nucleic Acids Res. 2021 Jan 8;49(D1):D1311-D1320. doi: 10.1093/nar/gkaa840.
5
Phase II Trials in Drug Development and Adaptive Trial Design.药物研发中的II期试验与适应性试验设计
JACC Basic Transl Sci. 2019 Jun 24;4(3):428-437. doi: 10.1016/j.jacbts.2019.02.005. eCollection 2019 Jun.
6
The support of human genetic evidence for approved drug indications.支持人类遗传证据用于批准的药物适应证。
Nat Genet. 2015 Aug;47(8):856-60. doi: 10.1038/ng.3314. Epub 2015 Jun 29.
7
Genotype to phenotype via network analysis.通过网络分析进行基因型到表型的研究。
Curr Opin Genet Dev. 2013 Dec;23(6):611-21. doi: 10.1016/j.gde.2013.10.003. Epub 2013 Nov 14.