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InvFEST,一个整合了人类基因组中多态性倒位信息的数据库。

InvFEST, a database integrating information of polymorphic inversions in the human genome.

机构信息

Institut de Biotecnologia i de Biomedicina, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain, Departament de Genètica i de Microbiologia, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain and Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.

出版信息

Nucleic Acids Res. 2014 Jan;42(Database issue):D1027-32. doi: 10.1093/nar/gkt1122. Epub 2013 Nov 18.

Abstract

The newest genomic advances have uncovered an unprecedented degree of structural variation throughout genomes, with great amounts of data accumulating rapidly. Here we introduce InvFEST (http://invfestdb.uab.cat), a database combining multiple sources of information to generate a complete catalogue of non-redundant human polymorphic inversions. Due to the complexity of this type of changes and the underlying high false-positive discovery rate, it is necessary to integrate all the available data to get a reliable estimate of the real number of inversions. InvFEST automatically merges predictions into different inversions, refines the breakpoint locations, and finds associations with genes and segmental duplications. In addition, it includes data on experimental validation, population frequency, functional effects and evolutionary history. All this information is readily accessible through a complete and user-friendly web report for each inversion. In its current version, InvFEST combines information from 34 different studies and contains 1092 candidate inversions, which are categorized based on internal scores and manual curation. Therefore, InvFEST aims to represent the most reliable set of human inversions and become a central repository to share information, guide future studies and contribute to the analysis of the functional and evolutionary impact of inversions on the human genome.

摘要

最新的基因组进展揭示了基因组中前所未有的结构变异程度,大量数据正在迅速积累。在这里,我们介绍 InvFEST(http://invfestdb.uab.cat),这是一个结合了多种信息来源的数据库,用于生成非冗余人类多态性倒位的完整目录。由于这种类型的变化的复杂性和潜在的高假阳性发现率,有必要整合所有可用的数据,以获得倒位的真实数量的可靠估计。InvFEST 自动将预测合并到不同的倒位中,细化断点位置,并发现与基因和片段重复的关联。此外,它还包含关于实验验证、种群频率、功能效应和进化历史的数据。所有这些信息都可以通过每个倒位的完整且用户友好的网络报告轻松访问。在当前版本中,InvFEST 结合了来自 34 项不同研究的信息,包含 1092 个候选倒位,这些倒位基于内部评分和手动注释进行分类。因此,InvFEST 旨在代表最可靠的人类倒位集,并成为一个共享信息的中心存储库,指导未来的研究,并有助于分析倒位对人类基因组的功能和进化影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ea/3965118/51d2634f4c0a/gkt1122f1p.jpg

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