This will significantly reduce the numbers of errors incorporated into a sequence (compared to the current approach of amplifying multiple copies), allowing the genome of an individual cell to be read more accurately and enable advances in functional genomics and proteomics.
这可以大大减少测序错误(与目前的多拷贝扩增做法相比)，能够更准确地读出个别细胞的基因组，并促进功能基因组学和蛋白质组学的发展。