Cho Michael H, Ciulla Dawn, Klanderman Barbara J, Raby Benjamin A, Silverman Edwin K
Channing Laboratory, Brigham and Women's Hospital, Boston, MA 02115, USA.
Clin Chem. 2008 Dec;54(12):2055-8. doi: 10.1373/clinchem.2008.109744.
High-resolution melting curve analysis is an accurate method for mutation detection in genomic DNA. Few studies have compared the performance of high-resolution DNA melting curve analysis (HRM) in genomic and whole-genome amplified (WGA) DNA.
In 39 paired genomic and WGA samples, 23 amplicons from 9 genes were PCR amplified and analyzed by high-resolution melting curve analysis using the 96-well LightScanner (Idaho Technology). We used genotyping and bidirectional resequencing to verify melting curve results.
Melting patterns were concordant between the genomic and WGA samples in 823 of 863 (95%) analyzed sample pairs. Of the discordant patterns, there was an overrepresentation of alternate melting curve patterns in the WGA samples, suggesting the presence of a mutation (false positives). Targeted resequencing in 135 genomic and 136 WGA samples revealed 43 single nucleotide polymorphisms (SNPs). All SNPs detected in genomic samples were also detected in WGA. Additional genotyping and sequencing allowed the classification of 628 genomic and 614 WGA amplicon samples. Heterozygous variants were identified by non-wild-type melting pattern in 98% of genomic and 97% of WGA samples (P = 0.11). Wild types were correctly classified in 99% of genomic and 91% of WGA samples (P < 0.001).
In WGA DNA, high-resolution DNA melting curve analysis is a sensitive tool for SNP discovery through detection of heterozygote variants; however, it may misclassify a greater number of wild-type samples.
高分辨率熔解曲线分析是检测基因组DNA中突变的一种准确方法。很少有研究比较高分辨率DNA熔解曲线分析(HRM)在基因组DNA和全基因组扩增(WGA)DNA中的性能。
在39对配对的基因组和WGA样本中,对来自9个基因的23个扩增子进行PCR扩增,并使用96孔LightScanner(Idaho Technology)通过高分辨率熔解曲线分析进行分析。我们使用基因分型和双向重测序来验证熔解曲线结果。
在863对分析样本中,有823对(95%)基因组和WGA样本的熔解模式一致。在不一致的模式中,WGA样本中交替熔解曲线模式的比例过高,提示存在突变(假阳性)。对135个基因组样本和136个WGA样本进行靶向重测序,发现了43个单核苷酸多态性(SNP)。在基因组样本中检测到的所有SNP在WGA样本中也均被检测到。进一步的基因分型和测序对628个基因组扩增子样本和614个WGA扩增子样本进行了分类。在98%的基因组样本和97%的WGA样本中,通过非野生型熔解模式鉴定出杂合变异(P = 0.11)。在99%的基因组样本和91%的WGA样本中,野生型被正确分类(P < 0.001)。
在WGA DNA中,高分辨率DNA熔解曲线分析是通过检测杂合子变异发现SNP的一种敏感工具;然而,它可能会错误分类更多的野生型样本。