Hubrecht Institute, Developmental Biology and Stem Cell Research, Royal Netherlands Academy of Arts and Sciences and the University Medical Center Utrecht, Utrecht, The Netherlands.
Nat Methods. 2010 Nov;7(11):913-5. doi: 10.1038/nmeth.1516. Epub 2010 Oct 17.
Targeted genomic enrichment followed by next-generation DNA sequencing has dramatically increased efficiency of mutation-discovery efforts. We describe a protocol for genomic enrichment of pooled barcoded samples in a single assay that increases experimental flexibility and efficiency. We screened 770 genes (1.4 megabases) in thirty N-ethyl-N-nitrosourea (ENU)-mutagenized rats and identified known variants at >96% sensitivity as well as new mutations at a false positive rate < 1 in 8 megabases.
靶向基因组富集,然后进行下一代 DNA 测序,极大地提高了突变发现工作的效率。我们描述了一种在单个测定中对汇集的条形码样本进行基因组富集的方案,该方案提高了实验的灵活性和效率。我们对 30 只 N-乙基-N-亚硝脲(ENU)诱变大鼠的 770 个基因(1.4 兆碱基)进行了筛选,发现已知变体的灵敏度超过 96%,而在 8 兆碱基中假阳性率小于 1 的新突变。