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

机译:全基因组新生儿干血斑DNA的高质量外显子组测序

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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.
机译:新生儿筛查程序中存储的新生儿干血斑(DBS)样品是宝贵的诊断和研究资源。结合国家卫生注册处的信息,它们可用于基于人群的遗传疾病研究。可以扩增从新生儿DBS中提取的DNA,以获得微克形式的原本有限的资源,称为全基因组扩增DNA(wgaDNA)。在这里,我们研究了新生儿DBS样本的wgaDNA外显子组测序的稳健性。我们分别对七个,八个和七个主题进行了三个试点研究。对于每个受试者,我们分析了新生儿DBS样本和相应的成人全血(WB)参考样本。为每个受试者准备了不同的DNA样品类型。试验1:2x3.2mm新生儿DBS的wgaDNA(DBS_2x3.2)和WB参考样品的原始DNA提取物(WB_ref)。飞行员2:DBS_2x3.2,WB_ref和WB_ref副本与WB_ref样本共享DNA提取物。试点3:DBS_2x3.2,WB_ref,2x1.6毫米新生儿DBS的wgaDNA和WB参考样品的wgaDNA。经过排序和数据分析之后,我们比较了成对变体调用,以求得相似度的衡量标准(一致性率)。比较DBS与WB样本类型时,一致性率比过滤变体检出之前相同受试者的任意两个WB样本类型的一致性率略低。总体一致性率取决于变体类型,其中SNP表现最佳。后过滤后,DBS与WB以及WB与WB样本类型的比较得出相似的一致性率,其值接近100%。新生儿DBS样品的WgaDNA在外显子组测序中具有很高的准确性和效率。 wgaDNA的表现与匹配的高质量参照物(全血DNA)相似,其依据是通过变异调用计算出的一致性比率。用2x1.6毫米的圆盘代替2x3.2的圆盘没有观察到差异,从而可以在以后的项目中进一步减少样品材料。

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