Barson Gemma, Griffiths Ed
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
BMC Res Notes. 2016 Jan 22;9:39. doi: 10.1186/s13104-016-1847-3.
Manual annotation is essential to create high-quality reference alignments and annotation. Annotators need to be able to view sequence alignments in detail. The SeqTools package provides three tools for viewing different types of sequence alignment: Blixem is a many-to-one browser of pairwise alignments, displaying multiple match sequences aligned against a single reference sequence; Dotter provides a graphical dot-plot view of a single pairwise alignment; and Belvu is a multiple sequence alignment viewer, editor, and phylogenetic tool. These tools were originally part of the AceDB genome database system but have been completely rewritten to make them generally available as a standalone package of greatly improved function.
Blixem is used by annotators to give a detailed view of the evidence for particular gene models. Blixem displays the gene model positions and the match sequences aligned against the genomic reference sequence. Annotators use this for many reasons, including to check the quality of an alignment, to find missing/misaligned sequence and to identify splice sites and polyA sites and signals. Dotter is used to give a dot-plot representation of a particular pairwise alignment. This is used to identify sequence that is not represented (or is misrepresented) and to quickly compare annotated gene models with transcriptional and protein evidence that putatively supports them. Belvu is used to analyse conservation patterns in multiple sequence alignments and to perform a combination of manual and automatic processing of the alignment. High-quality reference alignments are essential if they are to be used as a starting point for further automatic alignment generation.
While there are many different alignment tools available, the SeqTools package provides unique functionality that annotators have found to be essential for analysing sequence alignments as part of the manual annotation process.
人工注释对于创建高质量的参考比对和注释至关重要。注释人员需要能够详细查看序列比对。SeqTools软件包提供了三种用于查看不同类型序列比对的工具:Blixem是一个用于双序列比对的多对一浏览器,可显示与单个参考序列比对的多个匹配序列;Dotter提供单个双序列比对的图形化点阵视图;而Belvu是一个多序列比对查看器、编辑器和系统发育工具。这些工具最初是AceDB基因组数据库系统的一部分,但已被完全重写,以便作为功能大幅改进的独立软件包普遍可用。
注释人员使用Blixem来详细查看特定基因模型的证据。Blixem显示基因模型位置以及与基因组参考序列比对的匹配序列。注释人员出于多种原因使用它,包括检查比对的质量、查找缺失/错配的序列以及识别剪接位点、多聚腺苷酸位点和信号。Dotter用于给出特定双序列比对的点阵表示。这用于识别未呈现(或呈现错误)的序列,并快速将注释的基因模型与可能支持它们的转录和蛋白质证据进行比较。Belvu用于分析多序列比对中的保守模式,并对比对进行手动和自动处理相结合的操作。如果要将高质量的参考比对用作进一步自动比对生成的起点,那么它们至关重要。
虽然有许多不同的比对工具可用,但SeqTools软件包提供了独特的功能,注释人员发现这些功能对于在人工注释过程中分析序列比对至关重要。