Hamoy Igor G, Ribeiro-Dos-Santos André M, Alvarez Luiz, Barbosa Silvanira, Silva Artur, Santos Sidney, Gusmão Leonor, Ribeiro-Dos-Santos Andrea
Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil. ; Universidade Federal Rural da Amazônia, Campus de Capanema, PA, Brazil.
Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.
Bioinform Biol Insights. 2014 Jun 11;8:127-34. doi: 10.4137/BBI.S14623. eCollection 2014.
The mitochondrial genome is widely studied in a variety of fields, such as population, forensic, and human and medical genetics. Most studies have been limited to a small portion of the sequence that, although highly diverse, does not describe the total variability. The arrival of modern high-throughput sequencing technologies has made it possible to investigate larger sequences in a shorter amount of time as well as in a more affordable fashion. This work aims to describe a protocol for sequencing and analyzing the complete mitochondrial genome with the Ion PGM™ platform. To evaluate the protocol, the mitochondrial genome was sequenced to approximately 210 Mbp, with high-quality sequences distributed between 12 samples that had an average coverage of 1023× per sample. Several variant callers were compared to improve the protocol outcome. The results suggest that it is possible to run up to 120 samples per run without any loss of any significant quality. Therefore, this protocol is an efficient and accurate tool for full mitochondrial genome analysis.
线粒体基因组在多个领域得到广泛研究,如群体遗传学、法医学以及人类与医学遗传学。大多数研究局限于线粒体基因组序列的一小部分,尽管这部分序列高度多样,但无法描述其全部变异性。现代高通量测序技术的出现,使得在更短时间内以更经济的方式研究更长的序列成为可能。本研究旨在描述一种使用Ion PGM™平台对完整线粒体基因组进行测序和分析的方案。为评估该方案,对线粒体基因组进行了约210 Mbp的测序,高质量序列分布在12个样本中,每个样本的平均覆盖度为1023×。比较了几种变异检测软件以优化方案结果。结果表明,每次运行最多可检测120个样本,且不会显著损失任何质量。因此,该方案是进行完整线粒体基因组分析的一种高效且准确的工具。