annotation

注释
  • 文章类型: Journal Article
    病理学中可靠的人工智能(AI)算法的发展通常取决于整张幻灯片图像(WSI)注释所提供的地面实况,一个耗时且依赖于操作员的过程。对不同注释方法进行了比较分析,以简化此过程。两名病理学家使用半自动化(SegmentAnythingModel,SAM))和手动设备(触摸板与鼠标)。在工作时间方面进行了比较,再现性(重叠分数),和精度(0到10精度由两个专家的肾病理学家评定)在不同的方法和操作。评价了不同显示器对小鼠性能的影响。注释集中在三个组织区室:小管(57注释),肾小球(53个注释),和动脉(58注释)。半自动方法是最快的,观察者之间的可变性最小,平均13.6±0.2min,差值(Δ)为2%,其次是小鼠(29.9±10.2,Δ=24%),和触摸板(47.5±19.6分钟,Δ=45%)。使用SAM可实现小管和肾小球的最高再现性(重叠值为1和0.99,而鼠标为0.97,触摸板为0.94和0.93),尽管SAM在动脉中的可重复性较低(与鼠标和触摸板的0.94相比,重叠值为0.89)。在操作者之间没有观察到精度差异(p=0.59)。使用非医疗显示器将注释时间增加了6.1%。未来采用半自动和人工智能辅助方法可以显著加快注释过程。改善AI工具开发的真相。
    The development of reliable artificial intelligence (AI) algorithms in pathology often depends on ground truth provided by annotation of whole slide images (WSI), a time-consuming and operator-dependent process. A comparative analysis of different annotation approaches is performed to streamline this process. Two pathologists annotated renal tissue using semi-automated (Segment Anything Model, SAM)) and manual devices (touchpad vs mouse). A comparison was conducted in terms of working time, reproducibility (overlap fraction), and precision (0 to 10 accuracy rated by two expert nephropathologists) among different methods and operators. The impact of different displays on mouse performance was evaluated. Annotations focused on three tissue compartments: tubules (57 annotations), glomeruli (53 annotations), and arteries (58 annotations). The semi-automatic approach was the fastest and had the least inter-observer variability, averaging 13.6 ± 0.2 min with a difference (Δ) of 2%, followed by the mouse (29.9 ± 10.2, Δ = 24%), and the touchpad (47.5 ± 19.6 min, Δ = 45%). The highest reproducibility in tubules and glomeruli was achieved with SAM (overlap values of 1 and 0.99 compared to 0.97 for the mouse and 0.94 and 0.93 for the touchpad), though SAM had lower reproducibility in arteries (overlap value of 0.89 compared to 0.94 for both the mouse and touchpad). No precision differences were observed between operators (p = 0.59). Using non-medical monitors increased annotation times by 6.1%. The future employment of semi-automated and AI-assisted approaches can significantly speed up the annotation process, improving the ground truth for AI tool development.
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  • 文章类型: Journal Article
    我们使用牛津纳米孔长读测序和Illumina短读测序报告了DiaportheaustralafricanaCrous和J.M.vanNiekerkusing的全基因组序列。杂种基因组由11个重叠群组成,总长度为53.509Mb,GC含量为52.40%。
    We report the whole-genome sequence of Diaporthe australafricana Crous & J.M. van Niekerkusing using Oxford Nanopore long-read sequencing and Illumina short-read sequencing. The hybrid genome consists of 11 contigs with a total length of 53.509 Mb, and a GC content of 52.40%.
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  • 文章类型: Journal Article
    背景:卷心菜网虫,Hellulaundalis(Fabricius)(鳞翅目:Pyralidae),是全球温暖地区的芸苔属植物和其他十字花科植物的重要害虫。转录组分析对于研究昆虫发育和繁殖的分子机制很有价值。当没有可用的参考基因组时,从头组装对于获得昆虫物种的完整转录组信息特别有用。在Hellula的情况下,目前整个NCBI核苷酸数据库中只有17个核苷酸记录。与代谢过程相关的基因,一般发展,繁殖,防御和功能基因组学先前未在基因组水平上预测。
    结果:要解决此问题,我们使用IlluminaNovaSeq6000技术构建了Hellulaundalis转录组。从测序获得大约48百万个150bp的配对末端读数。通过样品的从头组装产生了总共30,451个重叠群,并将其与NCBI非冗余蛋白质数据库(Nr)中的序列进行了比较。总的来说,71%的重叠群与公共数据库中的已知蛋白质匹配,包括Nr,基因本体论(GO),和集群直系同源基因数据库(COG),然后,通过针对京都基因百科全书和基因组途径数据库(KEGG)的功能注释,将重叠群映射到123。此外,我们比较了Hullulaundalis的直系同源基因家族,节食夜蛾的转录组,斜纹夜蛾和斜纹夜蛾,发现391个直系同源基因家族是绿叶夜蛾特有的。在Hullulaundalis重叠群中发现了总共1,913个潜在的SSR。
    结论:这项研究是Hullulaundalis的第一个转录组数据。此外,它是识别目标基因和开发有效和环境友好的虫害防治策略的宝贵资源。
    BACKGROUND: The cabbage webworm, Hellula undalis (Fabricius) (Lepidoptera: Pyralidae), is a significant pest of brassicas and other cruciferous plants in warm regions worldwide. Transcriptome analysis is valuable for investigation of molecular mechanisms underlying the insect development and reproduction. De novo assembly is particularly useful for acquiring complete transcriptome information of insect species when there is no reference genome available. In case of Hellula undalis, only 17 nucleotide records are currently available throughout NCBI nucleotide database. Genes associated with metabolic processes, general development, reproduction, defense and functional genomics were not previously predicted in the Hellula undalis at the genomic level.
    RESULTS: To address this issue, we constructed Hellula undalis transcriptome using Illumina NovaSeq6000 technology. Approximately 48 million 150 bp paired-end reads were obtained from sequencing. A total of 30,451 contigs were generated by de novo assembly of sample and were compared with the sequences in the NCBI non-redundant protein database (Nr). In total, 71 % of contigs were matched to known proteins in public databases including Nr, Gene Ontology (GO), and Cluster Orthologous Gene Database (COG), and then, contigs were mapped to 123 via functional annotation against the Kyoto Encyclopedia of Genes and Genomes pathway database (KEGG). In addition, we compared the ortholog gene family of the Hullula undalis, transcriptome to Spodoptera frugiperda, spodotera litura and spodoptera littoralis and found that 391 orthologous gene families are specific to Hullula undalis. A total of 1,913 potential SSRs was discovered in Hullula undalis contigs.
    CONCLUSIONS: This study is the first transcriptome data for Hullula undalis. Additionally, it serves as a valuable resource for identifying target genes and developing effective and environmentally friendly strategies for pest control.
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  • 文章类型: Journal Article
    背景:整合来自代表不同研究设计的数据源的信息有可能加强人口健康研究的证据。然而,这种“三角测量”的证据概念对系统地识别和整合相关信息提出了许多挑战。其中包括异构证据与共同语义概念和属性的协调,以及检索到的证据的优先级与感兴趣的问题的三角测量。
    结果:我们提供ASQ(带注释的语义查询),在EpiGraphDB中集成生物医学实体和流行病学证据的自然语言查询接口,它使用户能够从一段非结构化文本中提取“声明”,然后调查可能支持的证据,矛盾的说法,或为查询提供其他信息。这种方法有可能支持对预印本的快速审查,赠款申请,会议摘要和提交同行评审的文章。ASQ实施策略来协调不同分类中的生物医学实体和来自不同来源的证据,以促进证据的三角剖分和解释。
    方法:ASQ可在https://asq上公开获得。epigraphdb.org及其源代码可在GPL-3.0许可证下在https://github.com/mrcieu/epigraphdb-asq获得。
    背景:可以在补充材料以及通过https://asq在ASQ平台上找到更多信息。epigraphdb.org/docs.
    BACKGROUND: Integrating information from data sources representing different study designs has the potential to strengthen evidence in population health research. However, this concept of evidence \"triangulation\" presents a number of challenges for systematically identifying and integrating relevant information. These include the harmonization of heterogenous evidence with common semantic concepts and properties, as well as the priortization of the retrieved evidence for triangulation with the question of interest.
    RESULTS: We present Annotated Semantic Queries (ASQ), a natural language query interface to the integrated biomedical entities and epidemiological evidence in EpiGraphDB, which enables users to extract \"claims\" from a piece of unstructured text, and then investigate the evidence that could either support, contradict the claims, or offer additional information to the query. This approach has the potential to support the rapid review of preprints, grant applications, conference abstracts, and articles submitted for peer review. ASQ implements strategies to harmonize biomedical entities in different taxonomies and evidence from different sources, to facilitate evidence triangulation and interpretation.
    METHODS: ASQ is openly available at https://asq.epigraphdb.org and its source code is available at https://github.com/mrcieu/epigraphdb-asq under GPL-3.0 license.
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  • 文章类型: Journal Article
    Xenia2是一种DV簇状放线菌噬菌体,可感染红藻NRRLB-16540。基因组是68,135bp,具有57.9%的GC含量和98个预测的蛋白质编码基因,其中33个具有预测功能。Xenia2具有具有内溶素(溶素A)和四种不同的holin样跨膜蛋白的裂解盒。
    Xenia2 is a DV cluster actinobacteriophage that infects Gordonia rubripertincta NRRL B-16540. The genome is 68,135bp, has a GC content of 57.9% and 98 predicted protein-coding genes, 33 of which have a predicted function. Xenia2 has a lysis cassette with an endolysin (lysin A) and four different holin-like transmembrane proteins.
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  • 文章类型: Journal Article
    使用现场收集的标本从总共10种原产于伊利诺伊州中部草原和稀树草原(美国)的昆虫物种中获得9种高质量的基因组组装:Mellillaxanthometata(鳞翅目:Geometridae),夜蛾(鞘翅目:Carabidae),原种(半翅目:连科),Coeliniussp.(膜翅目:布拉科),光晕(双翅目:绿翅目),腹部腕带(神经翅目:Myrmeleontidae),卡洛尼亚(半翅目:Achilidae),孔眼(半翅目:Cicadellidae),AtlanticaFlexia(半翅目:Cicadellidae)和Stictocaliabisonia(半翅目:Membracidae)。尽管一些样品的DNA产量极小(<0.1μg),但从单个样品制备测序文库是成功的。根据初始DNA产量,对每个样品调整额外的测序和组装工作流程。PacBio环状共识(CCS/HiFi)或连续长读取(CLR)文库用于对长度达50kb的DNA片段进行测序,与Illumina测序的链接读取(TellSeq文库)和用于支架和间隙填充的Omni-C文库。组装的基因组大小范围为135MB至3.2GB。组装的支架的数量范围为47至>13,000,每个组件的最长支架范围为〜23至439Mb。基因组完整性很高,BUSCO评分范围从最大基因组的85.5%完整性到最小基因组的98.8%完整性(Coeliniussp。).使用RepeatMasker和GenomeScope2估计了独特的含量,其范围从50.7%到75.8%,并且随着基因组大小的增加而大致下降。结构注释预测了测序物种的19,281-72,469个蛋白质模型。当时每个基因组的测序成本在3-5千美元之间,在高性能集群上平均约1600个CPU小时,并且需要使用PacBioHiFi数据对样品进行大约14小时的生物信息学分析。大多数组件将受益于进一步的手动管理,以纠正Omni-C接触图中的非对角线或耗尽信号所建议的可能的支架错位和易位。
    Field-collected specimens were used to obtain nine high-quality genome assemblies from a total of 10 insect species native to prairies and savannas of central Illinois (USA): Mellilla xanthometata (Lepidoptera: Geometridae), Stenolophus ochropezus (Coleoptera: Carabidae), Forcipata loca (Hemiptera: Cicadellidae), Coelinius sp. (Hymenoptera: Braconidae), Thaumatomyia glabra (Diptera: Chloropidae), Brachynemurus abdominalus (Neuroptera: Myrmeleontidae), Catonia carolina (Hemiptera: Achilidae), Oncometopia orbona (Hemiptera: Cicadellidae), Flexamia atlantica (Hemiptera: Cicadellidae) and Stictocephala bisonia (Hemiptera: Membracidae). Sequencing library preparation from single specimens was successful despite extremely small DNA yields (<0.1 μg) for some samples. Additional sequencing and assembly workflows were adapted to each sample depending on the initial DNA yield. PacBio circular consensus (CCS/HiFi) or continuous long reads (CLR) libraries were used to sequence DNA fragments up to 50 kb in length, with Illumina sequenced linked-reads (TellSeq libraries) and Omni-C libraries used for scaffolding and gap-filling. Assembled genome sizes ranged from 135 MB to 3.2 GB. The number of assembled scaffolds ranged from 47 to >13,000, with the longest scaffold per assembly ranging from ~23 to 439 Mb. Genome completeness was high, with BUSCO scores ranging from 85.5% completeness for the largest genome (Stictocephala bisonia) to 98.8% completeness for the smallest genome (Coelinius sp.). The unique content was estimated using RepeatMasker and GenomeScope2, which ranged from 50.7% to 75.8% and roughly decreased with increasing genome size. Structural annotation predicted a range of 19,281-72,469 protein models for sequenced species. Sequencing costs per genome at the time ranged from US$3-5k, averaged ~1600 CPU-hours on a high-performance cluster and required approximately 14 h of bioinformatics analyses with samples using PacBio HiFi data. Most assemblies would benefit from further manual curation to correct possible scaffold misjoins and translocations suggested by off-diagonal or depleted signals in Omni-C contact maps.
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  • 文章类型: Journal Article
    我们介绍了最大的腹部CT数据集(称为AbdomenAtlas),包括20,460个三维CT体积,来自不同人群的112家医院,地理位置,和设施。AbdomenAtlas在AI算法的帮助下,提供了由10名放射科医生组成的团队注释的673K高质量的腹部解剖结构面罩。我们首先让放射科专家手动注释5,246个CT卷中的22个解剖结构。在此之后,对剩余的CT体积执行半自动注释程序,放射科医生修改AI预测的注释,反过来,AI通过从修订的注释中学习来改善其预测。如此大规模,详细注释,和多中心数据集的需要有两个原因。首先,AbdomenAtlas为大规模人工智能开发提供了重要资源,品牌为大型预训练模型,这可以减轻专家放射科医生的注释工作量,从而转移到更广泛的临床应用中。其次,AbdomenAtlas建立了评估AI算法的大规模基准-我们用于测试算法的数据越多,我们可以更好地保证在复杂的临床场景中的可靠性能。ISBI和MICCAI挑战名为BodyMaps:Towards3DAtlas是使用我们的AbdomenAtlas的一个子集启动的,旨在刺激人工智能创新,并对细分精度进行基准测试,推理效率,和领域的可泛化性。我们希望我们的AbdomenAtlas能够为更大规模的临床试验奠定基础,并为医学影像界的从业者提供特殊的机会。代码,模型,和数据集可在https://www上获得。zongweiz.com/dataset。
    We introduce the largest abdominal CT dataset (termed AbdomenAtlas) of 20,460 three-dimensional CT volumes sourced from 112 hospitals across diverse populations, geographies, and facilities. AbdomenAtlas provides 673 K high-quality masks of anatomical structures in the abdominal region annotated by a team of 10 radiologists with the help of AI algorithms. We start by having expert radiologists manually annotate 22 anatomical structures in 5,246 CT volumes. Following this, a semi-automatic annotation procedure is performed for the remaining CT volumes, where radiologists revise the annotations predicted by AI, and in turn, AI improves its predictions by learning from revised annotations. Such a large-scale, detailed-annotated, and multi-center dataset is needed for two reasons. Firstly, AbdomenAtlas provides important resources for AI development at scale, branded as large pre-trained models, which can alleviate the annotation workload of expert radiologists to transfer to broader clinical applications. Secondly, AbdomenAtlas establishes a large-scale benchmark for evaluating AI algorithms-the more data we use to test the algorithms, the better we can guarantee reliable performance in complex clinical scenarios. An ISBI & MICCAI challenge named BodyMaps: Towards 3D Atlas of Human Body was launched using a subset of our AbdomenAtlas, aiming to stimulate AI innovation and to benchmark segmentation accuracy, inference efficiency, and domain generalizability. We hope our AbdomenAtlas can set the stage for larger-scale clinical trials and offer exceptional opportunities to practitioners in the medical imaging community. Codes, models, and datasets are available at https://www.zongweiz.com/dataset.
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  • 文章类型: Journal Article
    分析主动脉和左心室流出道(LVOT)的解剖结构对于经导管主动脉瓣植入术(TAVI)的风险评估和计划至关重要。对主动脉根和LVOT的全面分析需要通过分割提取患者个体解剖结构。深度学习在各种分割任务中表现出良好的性能。如果这被表述为监督问题,训练需要大量的注释数据。因此,最小化注释复杂性是可取的。
    我们提出了二维(2D)横截面注释和基于点云的表面重建,以训练用于主动脉根和LVOT的全自动3D分割网络。我们的稀疏注释方案可以轻松快速地生成主动脉根部等管状结构的训练数据。从分割结果来看,我们得出TAVI计划的临床相关参数.
    提出的2D横截面注释结果在观察者之间具有很高的一致性[Dice相似系数(DSC):0.94]。分割模型实现了0.90的DSC和0.96mm的平均表面距离。我们的方法实现了预测和注释之间的主动脉瓣环最大直径差0.45mm(观察者间方差:0.25mm)。
    所提出的方法促进了可重复的注释。注释允许训练主动脉根和LVOT的准确分割模型。分割结果有助于对TAVI计划进行可再现和可量化的测量。
    UNASSIGNED: Analyzing the anatomy of the aorta and left ventricular outflow tract (LVOT) is crucial for risk assessment and planning of transcatheter aortic valve implantation (TAVI). A comprehensive analysis of the aortic root and LVOT requires the extraction of the patient-individual anatomy via segmentation. Deep learning has shown good performance on various segmentation tasks. If this is formulated as a supervised problem, large amounts of annotated data are required for training. Therefore, minimizing the annotation complexity is desirable.
    UNASSIGNED: We propose two-dimensional (2D) cross-sectional annotation and point cloud-based surface reconstruction to train a fully automatic 3D segmentation network for the aortic root and the LVOT. Our sparse annotation scheme enables easy and fast training data generation for tubular structures such as the aortic root. From the segmentation results, we derive clinically relevant parameters for TAVI planning.
    UNASSIGNED: The proposed 2D cross-sectional annotation results in high inter-observer agreement [Dice similarity coefficient (DSC): 0.94]. The segmentation model achieves a DSC of 0.90 and an average surface distance of 0.96 mm. Our approach achieves an aortic annulus maximum diameter difference between prediction and annotation of 0.45 mm (inter-observer variance: 0.25 mm).
    UNASSIGNED: The presented approach facilitates reproducible annotations. The annotations allow for training accurate segmentation models of the aortic root and LVOT. The segmentation results facilitate reproducible and quantifiable measurements for TAVI planning.
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  • 文章类型: Journal Article
    作物生长监测对于作物和供应链管理都至关重要。传统的手动采样对于评估整个田地或所有田地中的作物生长的空间变异性是不可行的。同时,基于无人机的遥感可以对作物生长进行有效和无损的调查。需要各种特定于作物的训练图像数据集来使用深度学习模型从无人机图像中检测作物。具体来说,白菜的训练数据集有限。这篇数据文章包括田间带注释的卷心菜图像,以使用机器学习模型识别卷心菜。该数据集包含458个图像,其中17,621个带注释的卷心菜。图像大小约为500至1000像素正方形。由于这些卷心菜图像是在多年的整个生长季节从不同品种收集的,用这个数据集训练的深度学习模型将能够识别各种各样的白菜形状。在未来,该数据集不仅可以用于无人机,还可以用于陆基机器人应用,用于作物传感或相关的植物特定管理。
    Crop growth monitoring is essential for both crop and supply chain management. Conventional manual sampling is not feasible for assessing the spatial variability of crop growth within an entire field or across all fields. Meanwhile, UAV-based remote sensing enables the efficient and nondestructive investigation of crop growth. A variety of crop-specific training image datasets are needed to detect crops from UAV imagery using a deep learning model. Specifically, the training dataset of cabbage is limited. This data article includes annotated cabbage images in the fields to recognize cabbages using machine learning models. This dataset contains 458 images with 17,621 annotated cabbages. Image sizes are approximately 500 to 1000 pixel squares. Since these cabbage images were collected from different cultivars during the whole growing season over the years, deep learning models trained with this dataset will be able to recognize a wide variety of cabbage shapes. In the future, this dataset can be used not only in UAVs but also in land-based robot applications for crop sensing or associated plant-specific management.
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  • 文章类型: Journal Article
    全面而准确的基因组注释对于推断生物体的预测功能至关重要。存在许多工具来注释基因,基因簇,移动遗传元素,和其他多样化的特征。然而,这些工具和管道很难安装和运行,专门针对特定元素或特征,或缺少提供重要基因组背景的较大元素的注释。整合分析结果对于理解基因功能也很重要。为了应对这些挑战,我们介绍Beav注释管道。Beav是一个命令行工具,可以自动注释细菌基因组序列,移动遗传元素,分子系统和基因簇,关键监管功能,和其他元素。除了自定义模型之外,Beav还使用现有工具,脚本,和数据库来注释不同的元素,系统,和序列特征。结合了植物相关微生物的自定义数据库,以改善农业上重要的病原体和互生体中关键毒力和共生基因的注释。Beav包括任选的农杆菌特异性管道,其鉴定和分类致癌质粒并注释质粒特异性特征。完成所有分析后,注释被合并以产生单一的综合输出。最后,Beav生成出版物质量的基因组和质粒图谱。Beav位于Bioconda上,可从https://github.com/weisberglab/beav下载。
    目的:基因组特征的注释,比如基因的存在及其预测的功能,或编码分泌系统或生物合成基因簇的较大基因座,是理解有机体编码的功能所必需的。基因组还可以承载不同的可移动遗传元件,如整合和共轭元件和/或噬菌体,通常不被现有管道注释。这些元件可以水平移动编码毒力的基因,抗菌素耐药性,或其他适应性功能并改变生物体的表型。我们开发了一个软件管道,叫Beav,它结合了新的和现有的工具,对这些和其他主要功能进行了全面的注释。现有的管道经常错误地注释对植物相关细菌中的毒力或共生很重要的基因座。Beav包括自定义数据库和可选的工作流程,用于改进植物相关细菌的注释。Beav的设计易于安装和运行,使全面的基因组注释广泛提供给研究界。
    Comprehensive and accurate genome annotation is crucial for inferring the predicted functions of an organism. Numerous tools exist to annotate genes, gene clusters, mobile genetic elements, and other diverse features. However, these tools and pipelines can be difficult to install and run, be specialized for a particular element or feature, or lack annotations for larger elements that provide important genomic context. Integrating results across analyses is also important for understanding gene function. To address these challenges, we present the Beav annotation pipeline. Beav is a command-line tool that automates the annotation of bacterial genome sequences, mobile genetic elements, molecular systems and gene clusters, key regulatory features, and other elements. Beav uses existing tools in addition to custom models, scripts, and databases to annotate diverse elements, systems, and sequence features. Custom databases for plant-associated microbes are incorporated to improve annotation of key virulence and symbiosis genes in agriculturally important pathogens and mutualists. Beav includes an optional Agrobacterium-specific pipeline that identifies and classifies oncogenic plasmids and annotates plasmid-specific features. Following the completion of all analyses, annotations are consolidated to produce a single comprehensive output. Finally, Beav generates publication-quality genome and plasmid maps. Beav is on Bioconda and is available for download at https://github.com/weisberglab/beav.
    OBJECTIVE: Annotation of genome features, such as the presence of genes and their predicted function, or larger loci encoding secretion systems or biosynthetic gene clusters, is necessary for understanding the functions encoded by an organism. Genomes can also host diverse mobile genetic elements, such as integrative and conjugative elements and/or phages, that are often not annotated by existing pipelines. These elements can horizontally mobilize genes encoding for virulence, antimicrobial resistance, or other adaptive functions and alter the phenotype of an organism. We developed a software pipeline, called Beav, that combines new and existing tools for the comprehensive annotation of these and other major features. Existing pipelines often misannotate loci important for virulence or mutualism in plant-associated bacteria. Beav includes custom databases and optional workflows for the improved annotation of plant-associated bacteria. Beav is designed to be easy to install and run, making comprehensive genome annotation broadly available to the research community.
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