. Genome-wide detection of single-nucleotide and copy-number variations of a single human cell. Science. 2012 Dec 21;338(6114):1622-6. PubMed.


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  1. Researchers began publishing the sequences of single cell genomes back in 2006 (Zhang et al., 2006), and the technology has continued to evolve until today (see Fan et al., 2010; Navin et al., 2011; Gundry et al., 2012; Hou et al., 2012; Wang et al., 2012). The improvement here lies in getting a smooth representation of the original DNA regions of the genome. Their method reduces variation and bias. This is very good for determining copy number variation. But another key component of accuracy (that the authors do not mention) is haplotype phase, which tells you if you have two mutations affecting both copies of a gene, or those same two mutations in only one copy, leaving the other copy unaffected. Knowing if you have one good copy or zero is a big deal for clinical (and research) accuracy. A combination of the MALBAC and long fragment read (LFR) methods would be ideal. Although previous work required more than one cell (Peters et al., 2012), note that here, Zong et al. also explicitly state, "our strategy to reduce the false positive rate was to sequence two or three kindred cells derived from the same cell."


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  1. New Method to Boost Single Cell Genomics