High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

被引:37
作者
Poulsen, Jesper Buchhave [1 ]
Lescai, Francesco [2 ,3 ,4 ]
Grove, Jakob [2 ,3 ,4 ,5 ]
Baekvad-Hansen, Marie [1 ]
Christiansen, Michael [6 ]
Hagen, Christian Munch [6 ]
Maller, Julian [7 ]
Stevens, Christine [7 ]
Li, Shenting [2 ,3 ,4 ]
Li, Qibin [8 ]
Sun, Jihua [9 ]
Wang, Jun [3 ,4 ,8 ]
Nordentoft, Merete [3 ,10 ]
Werge, Thomas Mears [3 ,11 ]
Mortensen, Preben Bo [3 ,12 ]
Borglum, Anders Dupont [2 ,3 ,4 ]
Daly, Mark [7 ]
Hougaard, David Michael [1 ,13 ]
Bybjerg-Grauholm, Jonas [1 ]
Hollegaard, Mads Vilhelm [1 ,13 ]
机构
[1] Statens Serum Inst, Dept Congenital Disorders, Danish Ctr Neonatal Screening, Sect Neonatal Genet, DK-2300 Copenhagen, Denmark
[2] Aarhus Univ, Dept Biomed, Aarhus, Denmark
[3] Aarhus Univ, iPSYCH Lundbeck Fdn Initiat Integrat Psychiat Res, Aarhus, Denmark
[4] Aarhus Univ, iSEQ Ctr Integrat Sequencing, Aarhus, Denmark
[5] Aarhus Univ, Bioinformat Res Ctr, Aarhus, Denmark
[6] Statens Serum Inst, Dept Congenital Disorders, Mol Med, DK-2300 Copenhagen, Denmark
[7] Stanley Ctr, Broad Inst, Cambridge, MA USA
[8] BGI Shenzhen, Shenzhen, Peoples R China
[9] BGI Europe AS, Copenhagen, Denmark
[10] Univ Copenhagen, Mental Hlth Ctr Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
[11] Capital Reg Denmark, Inst Biol Psychiat, Mental Hlth Ctr Sct Hans, Roskilde, Denmark
[12] Aarhus Univ, Natl Ctr Register Based Res, Sch Business & Social Sci, Aarhus, Denmark
[13] Statens Serum Inst, Dept Congenital Disorders, Danish Ctr Neonatal Screening, Danish Neonatal Screening Biobank, DK-2300 Copenhagen, Denmark
关键词
COMMON VARIANTS; NEWBORN; AMPLIFICATION; EXTRACTION; PROTEINS; CAPTURE; STORAGE;
D O I
10.1371/journal.pone.0153253
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Stored neonatal dried blood spot (DBS) samples from neonatal screening programmes are a valuable diagnostic and research resource. Combined with information from national health registries they can be used in population-based studies of genetic diseases. DNA extracted from neonatal DBSs can be amplified to obtain micrograms of an otherwise limited resource, referred to as whole-genome amplified DNA (wgaDNA). Here we investigate the robustness of exome sequencing of wgaDNA of neonatal DBS samples. We conducted three pilot studies of seven, eight and seven subjects, respectively. For each subject we analysed a neonatal DBS sample and corresponding adult whole-blood (WB) reference sample. Different DNA sample types were prepared for each of the subjects. Pilot 1: wgaDNA of 2x3.2mm neonatal DBSs (DBS_ 2x3.2) and raw DNA extract of the WB reference sample (WB_ ref). Pilot 2: DBS_2x3.2, WB_ref and a WB_ref replica sharing DNA extract with the WB_ ref sample. Pilot 3: DBS_2x3.2, WB_ref, wgaDNA of 2x1.6 mm neonatal DBSs and wgaDNA of the WB reference sample. Following sequencing and data analysis, we compared pairwise variant calls to obtain a measure of similarity-the concordance rate. Concordance rates were slightly lower when comparing DBS vs WB sample types than for any two WB sample types of the same subject before filtering of the variant calls. The overall concordance rates were dependent on the variant type, with SNPs performing best. Post-filtering, the comparisons of DBS vs WB and WB vs WB sample types yielded similar concordance rates, with values close to 100%. WgaDNA of neonatal DBS samples performs with great accuracy and efficiency in exome sequencing. The wgaDNA performed similarly to matched high-quality reference-whole-blood DNA-based on concordance rates calculated from variant calls. No differences were observed substituting 2x3.2 with 2x1.6 mm discs, allowing for additional reduction of sample material in future projects.
引用
收藏
页数:13
相关论文
共 31 条
[1]
Aoki Kikumaro, 2003, Southeast Asian Journal of Tropical Medicine and Public Health, V34, P80
[2]
Comprehensive comparison of three commercial human whole-exome capture platforms [J].
Asan ;
Xu, Yu ;
Jiang, Hui ;
Tyler-Smith, Chris ;
Xue, Yali ;
Jiang, Tao ;
Wang, Jiawei ;
Wu, Mingzhi ;
Liu, Xiao ;
Tian, Geng ;
Wang, Jun ;
Wang, Jian ;
Yang, Huangming ;
Zhang, Xiuqing .
GENOME BIOLOGY, 2011, 12 (09) :R95
[3]
Whole exome capture in solution with 3 Gbp of data [J].
Bainbridge, Matthew N. ;
Wang, Min ;
Burgess, Daniel L. ;
Kovar, Christie ;
Rodesch, Matthew J. ;
D'Ascenzo, Mark ;
Kitzman, Jacob ;
Wu, Yuan-Qing ;
Newsham, Irene ;
Richmond, Todd A. ;
Jeddeloh, Jeffrey A. ;
Muzny, Donna ;
Albert, Thomas J. ;
Gibbs, Richard A. .
GENOME BIOLOGY, 2010, 11 (06)
[4]
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci [J].
Borglum, A. D. ;
Demontis, D. ;
Grove, J. ;
Pallesen, J. ;
Hollegaard, M. V. ;
Pedersen, C. B. ;
Hedemand, A. ;
Mattheisen, M. ;
Uitterlinden, A. ;
Nyegaard, M. ;
Orntoft, T. ;
Wiuf, C. ;
Didriksen, M. ;
Nordentoft, M. ;
Noethen, M. M. ;
Rietschel, M. ;
Ophoff, R. A. ;
Cichon, S. ;
Yolken, R. H. ;
Hougaard, D. M. ;
Mortensen, P. B. ;
Mors, O. .
MOLECULAR PSYCHIATRY, 2014, 19 (03) :325-333
[5]
Analysis of multiple single nucleotide polymorphisms (SNP) on DNA traces from plasma and dried blood samples [J].
Catsburg, Arnold ;
van der Zwet, Wil C. ;
Morre, Servaas A. ;
Ouburg, Sander ;
Vandenbroucke-Grauls, Christina M. J. E. ;
Savelkoul, Paul H. M. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2007, 321 (1-2) :135-141
[6]
Performance comparison of exome DNA sequencing technologies [J].
Clark, Michael J. ;
Chen, Rui ;
Lam, Hugo Y. K. ;
Karczewski, Konrad J. ;
Chen, Rong ;
Euskirchen, Ghia ;
Butte, Atul J. ;
Snyder, Michael .
NATURE BIOTECHNOLOGY, 2011, 29 (10) :908-U206
[7]
Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis [J].
Feenstra, Bjarke ;
Geller, Frank ;
Krogh, Camilla ;
Hollegaard, Mads V. ;
Gortz, Sanne ;
Boyd, Heather A. ;
Murray, Jeffrey C. ;
Hougaard, David M. ;
Melbye, Mads .
NATURE GENETICS, 2012, 44 (03) :334-U1601
[8]
Epidemiology - When an entire country is a cohort [J].
Frank, L .
SCIENCE, 2000, 287 (5462) :2398-2399
[9]
Population-based screening for rare mutations: High-throughput DNA extraction and molecular amplification from Guthrie cards [J].
Hamvas, A ;
Trusgnich, M ;
Brice, H ;
Baumgartner, J ;
Hong, YL ;
Nogee, LM ;
Cole, FS .
PEDIATRIC RESEARCH, 2001, 50 (05) :666-668
[10]
Phenylketonuria screening registry as a resource for population genetic studies -: art. no. e60 [J].
Hannelius, U ;
Lindgren, CM ;
Melén, E ;
Malmberg, A ;
von Dobeln, U ;
Kere, J .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (10)