Next Generation-Targeted Amplicon Sequencing (NG-TAS): an optimised protocol and computational pipeline for cost-effective profiling of circulating tumour DNA

被引:12
作者
Gao, Meiling [1 ,2 ]
Callari, Maurizio [1 ,2 ]
Beddowes, Emma [1 ,2 ,3 ]
Sammut, Stephen-John [1 ,2 ]
Grzelak, Marta [1 ,2 ]
Biggs, Heather [3 ]
Jones, Linda [3 ]
Boumertit, Abdelhamid [3 ]
Linn, Sabine C. [4 ]
Cortes, Javier [5 ,6 ]
Oliveira, Mafalda [6 ]
Baird, Richard [3 ]
Chin, Suet-Feung [1 ,2 ]
Caldas, Carlos [1 ,2 ,3 ]
机构
[1] Univ Cambridge, Dept Oncol, Li Ka Shing Ctr, Cambridge CB2 0RE, England
[2] Univ Cambridge, Canc Res UK, Li Ka Shing Ctr, Cambridge Inst, Cambridge CB2 0RE, England
[3] Cambridge Univ Hosp NHS Fdn Trust, Canc Res UK, Breast Canc Programme, Cambridge Canc Ctr, Cambridge CB2 2QQ, England
[4] Netherland Canc Inst, NL-1006 BE Amsterdam, Netherlands
[5] Ramon y Cajal Univ Hosp, Madrid 28034, Spain
[6] Vall dHebron Inst Oncol, Barcelona 08035, Spain
基金
欧盟地平线“2020”;
关键词
NG-TAS; ctDNA; Liquid biopsy; Mutation; Multiplexing; Deep sequencing; Computational pipeline; Cancer; Heterogeneous; CANCER GENOMICS; MUTATIONS; PLASMA;
D O I
10.1186/s13073-018-0611-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Circulating tumour DNA (ctDNA) detection and monitoring have enormous potential clinical utility in oncology. We describe here a fast, flexible and cost-effective method to profile multiple genes simultaneously in low input cell-free DNA (cfDNA): Next Generation-Targeted Amplicon Sequencing (NG-TAS). We designed a panel of 377 amplicons spanning 20 cancer genes and tested the NG-TAS pipeline using cell-free DNA from two HapMap lymphoblastoid cell lines. NG-TAS consistently detected mutations in cfDNA when mutation allele fraction was >1%. We applied NG-TAS to a clinical cohort of metastatic breast cancer patients, demonstrating its potential in monitoring the disease. The computational pipeline is available at https://github.com/cclab-brca/NGTAS_pipeline.
引用
收藏
页数:14
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