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  1. Article

    Open Access

    The chromatin landscape of healthy and injured cell types in the human kidney

    There is a need to define regions of gene activation or repression that control human kidney cells in states of health, injury, and repair to understand the molecular pathogenesis of kidney disease and design ...

    Debora L. Gisch, Michelle Brennan, Blue B. Lake, Jeannine Basta in Nature Communications (2024)

  2. Article

    Open Access

    An atlas of healthy and injured cell states and niches in the human kidney

    Understanding kidney disease relies on defining the complexity of cell types and states, their associated molecular profiles and interactions within tissue neighbourhoods1. Here we applied multiple single-cell an...

    Blue B. Lake, Rajasree Menon, Seth Winfree, Qiwen Hu, Ricardo Melo Ferreira in Nature (2023)

  3. Article

    Open Access

    Author Correction: Comparative cellular analysis of motor cortex in human, marmoset and mouse

    Trygve E. Bakken, Nikolas L. Jorstad, Qiwen Hu, Blue B. Lake, Wei Tian in Nature (2022)

  4. No Access

    Article

    Scalable dual-omics profiling with single-nucleus chromatin accessibility and mRNA expression sequencing 2 (SNARE-seq2)

    Comprehensive characterization of cellular heterogeneity and the underlying regulatory landscapes of tissues and organs requires a highly robust and scalable method to acquire matched RNA and chromatin accessi...

    Nongluk Plongthongkum, Dinh Diep, Song Chen, Blue B. Lake, Kun Zhang in Nature Protocols (2021)

  5. Article

    Open Access

    Comparative cellular analysis of motor cortex in human, marmoset and mouse

    The primary motor cortex (M1) is essential for voluntary fine-motor control and is functionally conserved across mammals1. Here, using high-throughput transcriptomic and epigenomic profiling of more than 450,000 ...

    Trygve E. Bakken, Nikolas L. Jorstad, Qiwen Hu, Blue B. Lake, Wei Tian in Nature (2021)

  6. Article

    Open Access

    A perceptual scaling approach to eyewitness identification

    Eyewitness misidentification accounts for 70% of verified erroneous convictions. To address this alarming phenomenon, research has focused on factors that influence likelihood of correct identification, such a...

    Sergei Gepshtein, Yurong Wang, Fangchao He, Dinh Diep in Nature Communications (2020)

  7. No Access

    Article

    Reply to ‘DNA methylation haplotypes as cancer markers’

    Dinh Diep, Kun Zhang in Nature Genetics (2018)

  8. No Access

    Protocol

    Large-Scale Targeted DNA Methylation Analysis Using Bisulfite Padlock Probes

    Bisulfite padlock probes (BSPP) are a method for the targeted quantification of DNA methylation in mammalian genomes. They can simultaneously characterize the level of methylcytosine modification in a large nu...

    Dinh Diep, Nongluk Plongthongkum, Kun Zhang in DNA Methylation Protocols (2018)

  9. No Access

    Article

    Identification of methylation haplotype blocks aids in deconvolution of heterogeneous tissue samples and tumor tissue-of-origin map** from plasma DNA

    Kun Zhang and colleagues present a metric called methylation haplotype load (MHL) that quantifies methylation patterns within blocks of tightly linked CpG dinucleotides. They show that the MHL can distinguish ...

    Shicheng Guo, Dinh Diep, Nongluk Plongthongkum, Ho-Lim Fung, Kang Zhang in Nature Genetics (2017)

  10. Article

    Open Access

    Genome-wide analysis reveals TET-and TDG-mediated 5-methylcytosine oxidation dynamics

    Li Shen, Hao Wu, Dinh Diep, Ana C D’Alessio, Alan Fung in Epigenetics & Chromatin (2013)

  11. Article

    Open Access

    Genome-wide analysis reveals TET-and TDG-mediated 5-methylcytosine oxidation dynamics

    Li Shen, Hao Wu, Dinh Diep, Ana C D’Alessio, Alan Fung in Epigenetics & Chromatin (2013)

  12. Article

    Open Access

    5mC and 5hmC dynamics during PGC reprogramming and role of Tet1 in female meiosis

    Shinpei Yamaguchi, Kwonho Hong, Rui Liu, Li Shen, Azusa Inoue in Epigenetics & Chromatin (2013)

  13. No Access

    Article

    Tet1 controls meiosis by regulating meiotic gene expression

    A loss-of-function approach in mice is used to show that the methylcytosine dioxygenase Tet1 has a role in regulating meiosis and meiotic gene activation in female germ cells; Tet1 deficiency does not greatly ...

    Shinpei Yamaguchi, Kwonho Hong, Rui Liu, Li Shen, Azusa Inoue, Dinh Diep in Nature (2012)

  14. No Access

    Article

    Library-free methylation sequencing with bisulfite padlock probes

    The pairing of bisulfite padlock probes with a probe-design algorithm, library-free sequencing and an analysis pipeline provides a flexible and scalable method for quantifying cytosine methylation.

    Dinh Diep, Nongluk Plongthongkum, Athurva Gore, Ho-Lim Fung in Nature Methods (2012)

  15. Article

    The metabolome of induced pluripotent stem cells reveals metabolic changes occurring in somatic cell reprogramming

    Metabolism is vital to every aspect of cell function, yet the metabolome of induced pluripotent stem cells (iPSCs) remains largely unexplored. Here we report, using an untargeted metabolomics approach, that hu...

    Athanasia D Panopoulos, Oscar Yanes, Sergio Ruiz, Yasuyuki S Kida in Cell Research (2012)

  16. No Access

    Article

    Increased methylation variation in epigenetic domains across cancer types

    Andrew Feinberg and colleagues report whole-genome bisulfite sequencing of three colon cancers and matched normal tissue and two adenomatous polyps. The authors identify large blocks of relative hypomethylatio...

    Kasper Daniel Hansen, Winston Timp, Héctor Corrada Bravo in Nature Genetics (2011)

  17. Article

    Genome-wide map** of the sixth base

    Map** of 5-hydroxylmethylcytosine in mammalian genomes has unveiled its unique role in the epigenetic regulation of gene expression.

    Dinh Diep, Kun Zhang in Genome Biology (2011)

  18. No Access

    Article

    Recapitulation of premature ageing with iPSCs from Hutchinson–Gilford progeria syndrome

    The premature ageing disorder Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic condition characterized by a rapid onset of signs associated with normal ageing, such as atherosclerosis and the dege...

    Guang-Hui Liu, Basam Z. Barkho, Sergio Ruiz, Dinh Diep, **g Qu, Sheng-Lian Yang in Nature (2011)