Next-generation sequencing

被引：0
作者：
Jorge S Reis-Filho
机构：
[1] Institute of Cancer Research,Molecular Pathology Team, The Breakthrough Breast Cancer Research Centre
来源：
Breast Cancer Research | / 11卷
关键词：
Breast Cancer; Invasive Lobular Carcinoma; Cancer Genome; Parallel Sequencing; Copy Number Aberration;
D O I：
暂无
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摘要：
Next-generation sequencing (also known as massively parallel sequencing) technologies are revolutionising our ability to characterise cancers at the genomic, transcriptomic and epigenetic levels. Cataloguing all mutations, copy number aberrations and somatic rearrangements in an entire cancer genome at base pair resolution can now be performed in a matter of weeks. Furthermore, massively parallel sequencing can be used as a means for unbiased transcriptomic analysis of mRNAs, small RNAs and noncoding RNAs, genome-wide methylation assays and high-throughput chromatin immunoprecipitation assays. Here, I discuss the potential impact of this technology on breast cancer research and the challenges that come with this technological breakthrough.
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