Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten

被引:35
作者
Nair, Shalima S. [1 ,2 ]
Phuc-Loi Luu [1 ,2 ]
Qu, Wenjia [1 ]
Maddugoda, Madhavi [1 ,2 ]
Huschtscha, Lily [3 ]
Reddel, Roger [3 ]
Chenevix-Trench, Georgia [4 ]
Toso, Martina [4 ]
Kench, James G. [5 ,6 ]
Horvath, Lisa G. [6 ,7 ,8 ]
Hayes, Vanessa M. [1 ,2 ,6 ]
Stricker, Phillip D. [9 ]
Hughes, Timothy P. [10 ,11 ,12 ,13 ]
White, Deborah L. [10 ,11 ,14 ,15 ,16 ]
Rasko, John E. J. [17 ,18 ,19 ]
Wong, Justin J. -L. [17 ,18 ,20 ]
Clark, Susan J. [1 ,2 ,21 ]
机构
[1] Garvan Inst Med Res, Genom & Epigenet Div, Darlinghurst, NSW 2010, Australia
[2] UNSW, St Vincents Clin Sch, Sydney, NSW 2010, Australia
[3] Univ Sydney, Childrens Med Res Inst, Canc Res Unit, Westmead, NSW 2145, Australia
[4] QIMR Berghofer, Brisbane, Qld 4006, Australia
[5] Royal Prince Alfred Hosp, Dept Tissue Pathol & Diagnost Oncol, Camperdown, NSW, Australia
[6] Univ Sydney, Sydney Med Sch, Cent Clin Sch, Camperdown, NSW, Australia
[7] Garvan Inst Med Res, Kinghorn Canc Ctr, Clin Prostate Canc Res, Darlinghurst, NSW, Australia
[8] Chris OBrien Lifehouse, Camperdown, NSW, Australia
[9] St Vincents Hosp, Dept Urol, Darlinghurst, NSW, Australia
[10] South Australian Hlth & Med Res Inst, Canc Theme, Adelaide, SA, Australia
[11] Australian Leukaemia & Lymphoma Grp, Melbourne, Vic, Australia
[12] Univ Adelaide, Discipline Med, Adelaide, SA, Australia
[13] SA Pathol, Dept Haematol, Adelaide, SA, Australia
[14] Univ Adelaide, Fac Hlth Sci, Adelaide, SA, Australia
[15] Univ Adelaide, Fac Sci, Adelaide, SA, Australia
[16] Australian Genom Hlth Alliance, Melbourne, Vic, Australia
[17] Univ Sydney, Centenary Inst, Gene & Stem Cell Therapy Program, Camperdown, NSW 2050, Australia
[18] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[19] Royal Prince Alfred Hosp, Cell & Mol Therapies, Camperdown, NSW 2050, Australia
[20] Univ Sydney, Centenary Inst, Gene Regulat Canc Lab, Camperdown, NSW 2050, Australia
[21] Garvan Inst Med Res, Epigenet Res Program, 384 Victoria St, Sydney, NSW 2010, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
DNA methylation; Whole genome bisulphite sequencing; HiSeq X Ten; HiSeq; 2500; Epigenetics; SNP; METHYLATION ANALYSIS; HIGH-THROUGHPUT; CPG ISLANDS; CELLS; METHYLOME; HYPOMETHYLATION; DIFFERENTIATION; LANDSCAPES; CHALLENGES; RESOLUTION;
D O I
10.1186/s13072-018-0194-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Comprehensive genome-wide DNA methylation profiling is critical to gain insights into epigenetic reprogramming during development and disease processes. Among the different genome-wide DNA methylation technologies, whole genome bisulphite sequencing (WGBS) is considered the gold standard for assaying genome-wide DNA methylation at single base resolution. However, the high sequencing cost to achieve the optimal depth of coverage limits its application in both basic and clinical research. To achieve 15x coverage of the human methylome, using WGBS, requires approximately three lanes of 100-bp-paired-end Illumina HiSeq 2500 sequencing. It is important, therefore, for advances in sequencing technologies to be developed to enable cost-effective high-coverage sequencing. Results: In this study, we provide an optimised WGBS methodology, from library preparation to sequencing and data processing, to enable 16-20x genome-wide coverage per single lane of HiSeq X Ten, HCS 3.3.76. To process and analyse the data, we developed a WGBS pipeline (METH10X) that is fast and can call SNPs. We performed WGBS on both high-quality intact DNA and degraded DNA from formalin-fixed paraffin-embedded tissue. First, we compared different library preparation methods on the HiSeq 2500 platform to identify the best method for sequencing on the HiSeq X Ten. Second, we optimised the PhiX and genome spike-ins to achieve higher quality and coverage of WGBS data on the HiSeq X Ten. Third, we performed integrated whole genome sequencing (WGS) and WGBS of the same DNA sample in a single lane of HiSeq X Ten to improve data output. Finally, we compared methylation data from the HiSeq 2500 and HiSeq X Ten and found high concordance (Pearson r > 0.9x). Conclusions: Together we provide a systematic, efficient and complete approach to perform and analyse WGBS on the HiSeq X Ten. Our protocol allows for large-scale WGBS studies at reasonable processing time and cost on the HiSeq X Ten platform.
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页数:20
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