DeNoFo:用于标准化、可比较的从头基因注释的文件格式和工具包。

IF 5.4
Elias Dohmen, Margaux Aubel, Lars A Eicholt, Paul Roginski, Victor Luria, Amir Karger, Anna Grandchamp
{"title":"DeNoFo:用于标准化、可比较的从头基因注释的文件格式和工具包。","authors":"Elias Dohmen, Margaux Aubel, Lars A Eicholt, Paul Roginski, Victor Luria, Amir Karger, Anna Grandchamp","doi":"10.1093/bioinformatics/btaf539","DOIUrl":null,"url":null,"abstract":"<p><strong>Motivation: </strong>De novo genes emerge from previously non-coding regions of the genome, challenging the traditional view that new genes primarily arise through duplication and adaptation of existing ones. Characterised by their rapid evolution and their novel structural properties or functional roles, de novo genes represent a young area of research. Therefore, the field currently lacks established standards and methodologies, leading to inconsistent terminology and challenges in comparing and reproducing results.</p><p><strong>Results: </strong>This work presents a standardised annotation format to document the methodology of de novo gene datasets in a reproducible way. We developed DeNoFo, a toolkit to provide easy access to this format that simplifies annotation of datasets and facilitates comparison across studies. Unifying the different protocols and methods in one standardised format, while providing integration into established file formats, such as fasta or gff, ensures comparability of studies and advances new insights in this rapidly evolving field.</p><p><strong>Availability and implementation: </strong>DeNoFo is available through the official Python Package Index (PyPI) and at https://github.com/EDohmen/denofo. All tools have a graphical user interface and a command line interface. The toolkit is implemented in Python3, available for all major platforms and installable with pip and uv.</p>","PeriodicalId":93899,"journal":{"name":"Bioinformatics (Oxford, England)","volume":" ","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"DeNoFo: a file format and toolkit for standardised, comparable de novo gene annotation.\",\"authors\":\"Elias Dohmen, Margaux Aubel, Lars A Eicholt, Paul Roginski, Victor Luria, Amir Karger, Anna Grandchamp\",\"doi\":\"10.1093/bioinformatics/btaf539\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Motivation: </strong>De novo genes emerge from previously non-coding regions of the genome, challenging the traditional view that new genes primarily arise through duplication and adaptation of existing ones. Characterised by their rapid evolution and their novel structural properties or functional roles, de novo genes represent a young area of research. Therefore, the field currently lacks established standards and methodologies, leading to inconsistent terminology and challenges in comparing and reproducing results.</p><p><strong>Results: </strong>This work presents a standardised annotation format to document the methodology of de novo gene datasets in a reproducible way. We developed DeNoFo, a toolkit to provide easy access to this format that simplifies annotation of datasets and facilitates comparison across studies. Unifying the different protocols and methods in one standardised format, while providing integration into established file formats, such as fasta or gff, ensures comparability of studies and advances new insights in this rapidly evolving field.</p><p><strong>Availability and implementation: </strong>DeNoFo is available through the official Python Package Index (PyPI) and at https://github.com/EDohmen/denofo. All tools have a graphical user interface and a command line interface. The toolkit is implemented in Python3, available for all major platforms and installable with pip and uv.</p>\",\"PeriodicalId\":93899,\"journal\":{\"name\":\"Bioinformatics (Oxford, England)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioinformatics (Oxford, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/bioinformatics/btaf539\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioinformatics (Oxford, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/bioinformatics/btaf539","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

动机:新生基因从先前基因组的非编码区域出现,挑战了新基因主要通过复制和适应现有基因而产生的传统观点。de novo基因以其快速进化和新颖的结构特性或功能角色为特征,代表了一个年轻的研究领域。因此,该领域目前缺乏既定的标准和方法,导致术语不一致,并在比较和复制结果方面面临挑战。结果:这项工作提出了一种标准化的注释格式,以可重复的方式记录了新生基因数据集的方法。我们开发了DeNoFo,这是一个工具包,可以方便地访问这种格式,简化数据集的注释,并促进研究之间的比较。将不同的协议和方法统一为一种标准化格式,同时提供与已建立的文件格式(如fasta或gff)的集成,确保研究的可比性,并在这个快速发展的领域推进新的见解。可用性和实现:DeNoFo可通过官方Python包索引(PyPI)和https://github.com/EDohmen/denofo获得。所有工具都有图形用户界面和命令行界面。该工具包在Python3中实现,可用于所有主要平台,并可使用pip和uv安装。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DeNoFo: a file format and toolkit for standardised, comparable de novo gene annotation.

Motivation: De novo genes emerge from previously non-coding regions of the genome, challenging the traditional view that new genes primarily arise through duplication and adaptation of existing ones. Characterised by their rapid evolution and their novel structural properties or functional roles, de novo genes represent a young area of research. Therefore, the field currently lacks established standards and methodologies, leading to inconsistent terminology and challenges in comparing and reproducing results.

Results: This work presents a standardised annotation format to document the methodology of de novo gene datasets in a reproducible way. We developed DeNoFo, a toolkit to provide easy access to this format that simplifies annotation of datasets and facilitates comparison across studies. Unifying the different protocols and methods in one standardised format, while providing integration into established file formats, such as fasta or gff, ensures comparability of studies and advances new insights in this rapidly evolving field.

Availability and implementation: DeNoFo is available through the official Python Package Index (PyPI) and at https://github.com/EDohmen/denofo. All tools have a graphical user interface and a command line interface. The toolkit is implemented in Python3, available for all major platforms and installable with pip and uv.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信