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Family-Specific Degenerate Primer Design: A Tool to Design Consensus Degenerated Oligonucleotides

机译:家庭特定的简并引物设计:设计共识简并寡核苷酸的工具。

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摘要

Designing degenerate PCR primers for templates of unknown nucleotide sequence may be a very difficult task. In this paper, we present a new method to design degenerate primers, implemented in family-specific degenerate primer design (FAS-DPD) computer software, for which the starting point is a multiple alignment of related amino acids or nucleotide sequences. To assess their efficiency, four different genome collections were used, covering a wide range of genomic lengths: Arenavirus (10 × 104 nucleotides), Baculovirus (0.9 × 105 to 1.8 × 105 bp), Lactobacillus sp. (1 × 106 to 2 × 106 bp), and Pseudomonas sp. (4 × 106 to 7 × 106 bp). In each case, FAS-DPD designed primers were tested computationally to measure specificity. Designed primers for Arenavirus and Baculovirus were tested experimentally. The method presented here is useful for designing degenerate primers on collections of related protein sequences, allowing detection of new family members.
机译:为未知核苷酸序列的模板设计简并PCR引物可能是一项非常困难的任务。在本文中,我们提出了一种设计简并引物的新方法,该方法在家族特异性简并引物设计(FAS-DPD)计算机软件中实现,其起点是相关氨基酸或核苷酸序列的多重比对。为了评估其效率,我们使用了四个不同的基因组集合,涵盖了广泛的基因组长度:甲状旁腺病毒(10×10 4 核苷酸),杆状病毒(0.9×10 5 至1.8×10 5 bp),乳杆菌。 (1×10 6 到2×10 6 bp),和假单胞菌sp。 (4×10 6 到7×10 6 bp)。在每种情况下,都对FAS-DPD设计的引物进行了计算测试以测量特异性。通过实验测试了针对腔病毒和杆状病毒的引物。本文介绍的方法可用于设计相关蛋白质序列集合上的简并引物,从而可以检测新的家族成员。

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