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首页> 外文期刊>European journal of human genetics: EJHG >Ultralow amounts of DNA from long-term archived serum samples produce quality genotypes
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Ultralow amounts of DNA from long-term archived serum samples produce quality genotypes

机译:来自长期存档血清样品的DNA的超低量产生质量基因型

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While genotyping studies are scavenging for suitable samples to analyze, large serum collections are currently left unused as they are assumed to provide insufficient amounts of DNA for array-based genotyping. Long-term stored serum is considered to be difficult to genotype since preanalytical treatments and storage effects on DNA yields are not well understood. Successful genotyping of such samples has the potential to activate large biobanks for future genome-wide association studies (GWAS). We aimed to evaluate genotyping of ultralow amounts of DNA from samples stored up to 45 years in the Janus Serum Bank with two commercially available platforms. 64 samples, with various preanalytical treatments, were genotyped on the Axiom Array from Thermo Fisher Scientific and a subset of 24 samples with slightly higher yield were genotyped on the HumanCoreExome array from Illumina. Our results showed that about 80% of the serum samples produced call rates with the Axiom arrays that would be satisfactory in GWAS. The mean DNA yield was 5.8 ng as measured with PicoGreen, 3-6% of recommended yield. The failed samples had on average lower input amounts of DNA. All serum samples genotyped on the HumanCoreExome with a standard and FFPE protocol produced GWAS satisfactory call rates, with mean 97.57% and 98.35% call rates, respectively. The mean yield was 10.65 ng, 6% of the recommendations. Successful array-based genotyping of ultralow DNA yields from serum samples stored up to 45 years is possible. These results demonstrate the potential to activate large serum biobank collections for future studies.
机译:虽然基因分型研究是用于分析的合适样品的扫描,但是当前假设大量的血清收集是未使用的,因为它们被假定为基于阵列的基因分型的DNA量不足。长期储存的血清被认为是难以基因型,因为预先理解了对DNA产率的储存效应并不了解。这种样品的成功基因分型具有激活未来基因组关联研究(GWAS)的大型生物汉。我们的旨在评估在Janus血清库中储存的样品中的样品的超级DNA的基因分型,具有两个商业上可获得的平台。 64个样品,具有各种预审化治疗,在来自Thermo Fisher Scientific的公理阵列上基因分型,并且来自Illumina的豪华仪阵列的24个样品的子集。我们的研究结果表明,大约80%的血清样品用Axiom阵列产生了呼叫速率,在GWA中令人满意。用Picogreen测量的平均DNA产率为5.8ng,3-6%的推荐产率。失败的样本具有平均降低的DNA输入量。所有血清样品都以标准和FFPE协议在豪华仪上进行了基因分型,并产生了GWAS令人满意的呼叫率,分别为97.57%和98.35%的呼叫率。平均产量为10.65 ng,占建议的6%。可以从血清样品中储存长达45年的血清样品的超阵列基于阵列的基于阵列的基因分型。这些结果证明了激活大型血清BioBank系列以备将来的研究。

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