A dot-matrix program with dynamic threshold control suited for genomic DNA and protein sequence analysis

点阵 缩放 计算机科学 粘粒 渲染(计算机图形) 基质(化学分析) 生物 人工智能 计算机图形学(图像) 算法 DNA 遗传学 古生物学 材料科学 复合材料 镜头(地质)
作者
Erik L. L. Sonnhammer,Richard Durbin
出处
期刊:Gene [Elsevier BV]
卷期号:167 (1-2): GC1-GC10 被引量:684
标识
DOI:10.1016/0378-1119(95)00714-8
摘要

Graphical dot-matrix plots can provide the most complete and detailed comparison of two sequences. Presented here is DOTTER2, a dot-plot program for X-windows which can compare DNA or protein sequences, and also DNA versus protein. The main novel feature of DOTTER is that the user can vary the stringency cutoffs interactively, so that the dot-matrix only needs to be calculated once. This is possible thanks to a 'Greyramp tool' that was developed to change the displayed stringency of the matrix by dynamically changing the greyscale rendering of the dots. The Greyramp tool allows the user to interactively change the lower and upper score limit for the greyscale rendering. This allows exploration of the separation between signal and noise, and fine-grained visualisation of different score levels in the dot-matrix. Other useful features are dot-matrix compression, mouse-controlled zooming, sequence alignment display and saving/loading of dot-matrices. Since the matrix only has to be calculated once and since the algorithm is fast and linear in space, DOTTER is practical to use even for sequences as long as cosmids. DOTTER was integrated in the gene-modelling module of the genomic database system ACEDB3. This was done via the homology viewer BLIXEM in a way that also allows segments from the BLAST suite of searching programs to be superimposed on top of the full dot-matrix. This feature can also be used for very quick finding of the strongest matches. As examples, we analyse a Caenorhabditis elegans cosmid with several tandem repeat families, and illustrate how DOTTER can improve gene modelling.
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