Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts.

Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts.
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针对癌症转录组的下一代测序可增强序列变体和新型融合转录本的检测。

DOI:
10.1186/gb-2009-10-10-r115
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发表时间:
2009
期刊:
影响因子:
12.3
通讯作者:
Gnirke A
Gnirke A
中科院分区:
生物学1区
文献类型:
--
作者:
Levin JZ;Berger MF;Adiconis X;Rogov P;Melnikov A;Fennell T;Nusbaum C;Garraway LA;Gnirke A

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靶向RNA-Seq将下一代测序与转录组相关子集的序列捕获相结合,可以增强对该子集的观察。通过将肿瘤cDNA文库中的序列与467种癌症相关基因的寡核苷酸探针杂交,该方法显示出高选择性,改进了突变检测,能够发现新的嵌合转录物,并提供了RNA表达数据。因此,靶向RNA-Seq产生了一组“高兴趣”基因的分子状态的增强视图。
Combining next-generation sequencing with capture of sequences from a relevant subset of a transcriptome produces an enhanced view of this subset Targeted RNA-Seq combines next-generation sequencing with capture of sequences from a relevant subset of a transcriptome. When testing by capturing sequences from a tumor cDNA library by hybridization to oligonucleotide probes specific for 467 cancer-related genes, this method showed high selectivity, improved mutation detection enabling discovery of novel chimeric transcripts, and provided RNA expression data. Thus, targeted RNA-Seq produces an enhanced view of the molecular state of a set of "high interest" genes.
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