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首页> 外文期刊>DNA Sequence: The Journal of DNA Sequencing and Mapping >DNA sequence error rates in Genbank records estimated using the mouse genome as a reference
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DNA sequence error rates in Genbank records estimated using the mouse genome as a reference

机译:Genbank记录中的DNA序列错误率以小鼠基因组为参考估计

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We estimate DNA sequence error rates in Genbank records containing protein-coding and non-coding DNA sequences by comparing sequences of the inbred mouse strain C57BL/6J, sequenced as part of the mouse genome project and independently by other laboratories. C57BL/6J was produced by more than 100 generations of brother-sister mating, and can be assumed to be virtually free of residual polymorphism and mutational variation, so differences between independent sequences can be attributed to error. The estimated single nucleotide error rate for coding DNA is 0.10% (SE 0.012%), which is substantially lower than previous estimates for error rates in Genbank accessions. The estimated single nucleotide error rate for intronic DNA sequences (0.22%; SE 0.051%) is significantly higher than the rate for coding DNA. Since error rates for the mouse genome sequence are very low, the vast majority of the errors we detected are likely to be in individual Genbank accessions. The frequency of insertion-deletion (indel) errors in non-coding DNA approaches that of single nucleotide errors in non-coding DNA, whereas indel errors are uncommon in coding sequences.
机译:我们通过比较近交小鼠品系C57BL / 6J的序列来估计Genbank记录中包含蛋白质编码和非编码DNA序列的DNA序列错误率,该序列作为小鼠基因组计划的一部分并由其他实验室独立测序。 C57BL / 6J是由100多个兄弟姐妹交配产生的,并且可以假定为几乎没有残留的多态性和突变变异,因此独立序列之间的差异可归因于错误。估计的编码DNA的单核苷酸错误率是0.10%(SE 0.012%),大大低于以前对Genbank入库的错误率的估计。内含子DNA序列的估计单核苷酸错误率(0.22%; SE 0.051%)显着高于编码DNA的率。由于小鼠基因组序列的错误率非常低,因此我们检测到的绝大多数错误很可能是由于个别Genbank入藏。非编码DNA中插入-缺失(插入/缺失)错误的频率接近非编码DNA中单核苷酸错误的插入频率,而插入/缺失错误在编码序列中并不常见。

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