The researchers identified mutations in the same gene in an additional eight cases using Sanger sequencing.

研究人员利用Sanger测序鉴定出另外八个病例中相同基因的突变。

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The Sanger Institute studies used powerful new DNA sequencing technologies to decode completely the genome of both tumour tissue and normal tissue from a lung cancer and a malignant melanoma patient.

桑格研究所开展的这项研究从一名肺癌患者和一名皮肤癌患者身上分别提取肿瘤细胞组织和正常细胞组织，运用新型高效的DNA测序技术对其基因组进行了全面破解。

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Once a variant looks like it might be a cause of disease, it is double-checked using Sanger sequencing, the older, more expensive process that was used to create the original draft of the human genome a decade ago.

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