首页> 美国卫生研究院文献>other >FNBtools: A Software to Identify Homozygous Lesions in Deletion Mutant Populations
【2h】

FNBtools: A Software to Identify Homozygous Lesions in Deletion Mutant Populations

机译:FNBtools:一种用于识别缺失突变人群中纯合病变的软件

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Deletion mutagenesis such as fast neutron bombardment (FNB) has been widely used for forward and reverse genetics studies in functional genomics. Traditionally, the time-consuming map-based cloning is used to locate causal deletions in deletion mutants. In recent years, comparative genomic hybridization (CGH) has been used to speed up and scale up the lesion identification process in deletion mutants. However, limitations of low accuracy and sensitivity for small deletions in the CGH approach are apparent. With the next generation sequencing (NGS) becoming affordable for most users, NGS-based bioinformatics tools are more appealing. Although several deletion callers are available, these tools are not efficient in detecting small deletions. Population-scale deletion callers that can identify both small and large deletions are rare. We were motivated to create a population-scale deletion detection tool, called FNBtools, to identify homozygous causal deletions in mutant populations by using NGS data. FNBtools is a tool to call deletions at a population-scale and to achieve high accuracy at different levels of coverage. In addition, FNBtools can detect both small and large deletions with the ability to identify unique deletions in a mutant pool by filtering deletions that exist in a wild-type or control pool. Furthermore, FNBtools is also able to visualize all identified deletions in a genome-wide scope by using Circos. From simulated data analysis, FNBtools outperforms four existing popular deletion callers in detecting small deletions at different coverage levels. To test the usefulness of FNBtools in real biological applications, we used it to analyze a salt-tolerant mutant in Medicago truncatula and identified the unique deletion locus that is tightly linked with this trait. The causal deletion in the mutant was confirmed by PCR amplification, sequencing and genetic linkage analyses. FNBtools can be used for homozygous deletion identification in any species with reference genome sequences. FNBtools is publicly available at: .
机译:诸如快速中子轰击(FNB)的缺失诱变已广泛用于功能基因组学中的正向和反向遗传学研究。传统上,耗时的基于图的克隆用于定位缺失突变体中的因果缺失。近年来,比较基因组杂交(CGH)已被用于加快和扩大缺失突变体中病灶的鉴定过程。但是,在CGH方法中对小缺失的准确性和敏感性低的局限性是显而易见的。随着大多数用户可以负担得起下一代测序(NGS)的需求,基于NGS的生物信息学工具更具吸引力。尽管有几个删除调用者可用,但是这些工具在检测小删除时效率不高。能够识别小和大缺失的人口规模的删除呼叫者很少。我们被激励创建一个称为FNBtools的人口规模的删除检测工具,以通过使用NGS数据来识别突变种群中的纯合因果缺失。 FNBtools是一种用于在人口规模上调用删除并在不同覆盖级别上实现高精度的工具。此外,FNBtools可以通过过滤野生型或对照池中存在的缺失来识别突变池中独特的缺失,从而检测出大小缺失。此外,FNBtools还能够使用Circos可视化全基因组范围内所有已识别的缺失。通过模拟数据分析,在检测覆盖范围不同的小缺失时,FNBtools优于四个现有的流行缺失调用者。为了测试FNBtools在实际生物学应用中的有用性,我们使用它分析了苜蓿苜蓿(Medicago truncatula)中的耐盐突变体,并确定了与该性状紧密相关的独特缺失位点。通过PCR扩增,测序和遗传连锁分析证实了突变体中的因果缺失。 FNBtools可用于具有参考基因组序列的任何物种的纯合缺失鉴定。 FNBtools可在以下位置公开获得。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号