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Using the miraEST Assembler for Reliable and Automated mRNA Transcript Assembly and SNP Detection in Sequenced ESTs

机译:使用miraEST汇编程序在测序的EST中进行可靠和自动化的mRNA转录产物组装和SNP检测

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摘要

We present an EST sequence assembler that specializes in reconstruction of pristine mRNA transcripts, while at the same time detecting and classifying single nucleotide polymorphisms (SNPs) occuring in different variations thereof. The assembler uses iterative multipass strategies centered on high-confidence regions within sequences and has a fallback strategy for using low-confidence regions when needed. It features special functions to assemble high numbers of highly similar sequences without prior masking, an automatic editor that edits and analyzes alignments by inspecting the underlying traces, and detection and classification of sequence properties like SNPs with a high specificity and a sensitivity down to one mutation per sequence. In addition, it includes possibilities to use incorrectly preprocessed sequences, routines to make use of additional sequencing information such as base-error probabilities, template insert sizes, strain information, etc., and functions to detect and resolve possible misassemblies. The assembler is routinely used for such various tasks as mutation detection in different cell types, similarity analysis of transcripts between organisms, and pristine assembly of sequences from various sources for oligo design in clinical microarray experiments.
机译:我们提出了一个EST序列组装商,专门从事原始mRNA转录物的重建,同时检测和分类发生在其不同变异中的单核苷酸多态性(SNP)。汇编程序使用以序列内高可信度区域为中心的迭代多遍策略,并在需要时具有使用低可信度区域的后备策略。它具有特殊功能,可在不事先掩盖的情况下组装大量高度相似的序列,自动编辑器可通过检查基础迹线来编辑和分析比对,并以高特异性和低至一个突变的敏感性对序列特性(如SNP)进行检测和分类每个序列。此外,它还包括使用不正确的预处理序列的可能性,利用其他测序信息(例如碱基错误概率,模板插入大小,应变信息等)的例程,以及检测和解决可能的错配的功能。组装程序通常用于各种任务,例如不同细胞类型中的突变检测,生物之间转录物的相似性分析以及来自原始来源的序列的原始组装,用于临床微阵列实验中的寡核苷酸设计。

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