Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity.

Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity.
复制标题

DOI:
10.1038/nmeth.3035
复制
发表时间:
2014-08
期刊:
影响因子:
48
通讯作者:
Kelsey, Gavin
Kelsey, Gavin
中科院分区:
生物学1区
文献类型:
--
作者:
Smallwood, Sebastien A.;Lee, Heather J.;Angermueller, Christof;Krueger, Felix;Saadeh, Heba;Peet, Julian;Andrews, Simon R.;Stegle, Oliver;Reik, Wolf;Kelsey, Gavin

文献摘要

参考文献

被引文献

相似文献

我们报告了一种单细胞亚硫酸氢盐测序方法(scBS-Seq),能够准确测量高达48.4%的CpG的DNA甲基化。我们观察到在血清或2 i中生长的ESC都显示出表观遗传异质性,血清培养物中存在“2 i样”细胞。12个小鼠卵母细胞数据集的计算机集成在很大程度上概括了整个DNA甲基化组,使scBS-Seq成为探索稀有细胞和异质群体中DNA甲基化的通用工具。
We report a single-cell bisulfite sequencing method (scBS-Seq) capable of accurately measuring DNA methylation at up to 48.4% of CpGs. We observed that ESCs grown in serum or 2i both display epigenetic heterogeneity, with “2i-like” cells present in serum cultures. In silico integration of 12 individual mouse oocyte datasets largely recapitulates the whole DNA methylome, making scBS-Seq a versatile tool to explore DNA methylation in rare cells and heterogeneous populations.
DOI: 10.1126/science.1247651
发表时间: 2014-02-14
期刊: Science (New York, N.Y.)
影响因子: --
作者:
Jaitin DA;Kenigsberg E;Keren-Shaul H;Elefant N;Paul F;Zaretsky I;Mildner A;Cohen N;Jung S;Tanay A;Amit I
通讯作者: Amit I
DOI: 10.1016/j.stem.2008.07.027
发表时间: 2008-10-09
期刊: Cell stem cell
影响因子: 23.9
作者:
Hayashi K;de Sousa Lopes SMC;Tang F;Lao K;Surani MA
通讯作者: Surani MA
DOI: 10.1038/ng.864
发表时间: 2011-06-26
期刊: Nature genetics
影响因子: 30.8
作者:
通讯作者: --
DOI: 10.1038/nature06403
发表时间: 2007-12-20
期刊: NATURE
影响因子: 64.8
作者:
Chambers, Ian;Silva, Jose;Smith, Austin
通讯作者: Smith, Austin
DOI: 10.1038/nature12433
发表时间: 2013-08-22
期刊: Nature
影响因子: 64.8
作者:
通讯作者: --