Dynamic Reprogramming of DNA Methylation at an Epigenetically Sensitive Allele in Mice

por Blewitt, Marnie E, Vickaryous, Nicola K, Paldi, Andras, Koseki, Haruhiko, Whitelaw, Emma
Publicado 2006

A comparison of control samples for ChIP-seq of histone modifications

por Flensburg, Christoffer, Kinkel, Sarah A., Keniry, Andrew, Blewitt, Marnie E., Oshlack, Alicia
Publicado 2014

Transcriptional profiling of the epigenetic regulator Smchd1

por Liu, Ruijie, Chen, Kelan, Jansz, Natasha, Blewitt, Marnie E., Ritchie, Matthew E.
Publicado 2015

Reduced dosage of the modifiers of epigenetic reprogramming Dnmt1, Dnmt3L, SmcHD1 and Foxo3a has no detectable effect on mouse telomere length in vivo

por Roberts, Amity R., Blewitt, Marnie E., Youngson, Neil A., Whitelaw, Emma, Chong, Suyinn
Publicado 2011

High concordance between Illumina HiSeq2500 and NextSeq500 for reduced representation bisulfite sequencing (RRBS)

por Yin, Danqing, Ritchie, Matthew E., Jabbari, Jafar S., Beck, Tamara, Blewitt, Marnie E., Keniry, Andrew
Publicado 2016

Relating SMCHD1 structure to its function in epigenetic silencing

por Gurzau, Alexandra D., Blewitt, Marnie E., Czabotar, Peter E., Murphy, James M., Birkinshaw, Richard W.
Publicado 2020

NanoMethViz: An R/Bioconductor package for visualizing long-read methylation data

por Su, Shian, Gouil, Quentin, Blewitt, Marnie E., Cook, Dianne, Hickey, Peter F., Ritchie, Matthew E.
Publicado 2021

Epigenetic modifier SMCHD1 maintains a normal pool of long-term hematopoietic stem cells

por Kinkel, Sarah A., Liu, Joy, Beck, Tamara, Breslin, Kelsey A., Iminitoff, Megan, Hickey, Peter, Blewitt, Marnie E.
Publicado 2022

The first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development

por Harten, Sarah K., Bruxner, Timothy J., Bharti, Vandhana, Blewitt, Marnie, Nguyen, Thi-My-Tam, Whitelaw, Emma, Epp, Trevor
Publicado 2014

Glimma: interactive graphics for gene expression analysis

por Su, Shian, Law, Charity W, Ah-Cann, Casey, Asselin-Labat, Marie-Liesse, Blewitt, Marnie E, Ritchie, Matthew E
Publicado 2017

Hippocampal neurogenesis mediates sex-specific effects of social isolation and exercise on fear extinction in adolescence

por Drummond, Katherine D., Waring, Michelle L., Faulkner, Geoffrey J., Blewitt, Marnie E., Perry, Christina J., Kim, Jee Hyun
Publicado 2021

Maternal SMCHD1 regulates Hox gene expression and patterning in the mouse embryo

por Benetti, Natalia, Gouil, Quentin, Tapia del Fierro, Andres, Beck, Tamara, Breslin, Kelsey, Keniry, Andrew, McGlinn, Edwina, Blewitt, Marnie E.
Publicado 2022

A method for stabilising the XX karyotype in female mESC cultures

por Keniry, Andrew, Jansz, Natasha, Hickey, Peter F., Breslin, Kelsey A., Iminitoff, Megan, Beck, Tamara, Gouil, Quentin, Ritchie, Matthew E., Blewitt, Marnie E.
Publicado 2022

ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activity

por Young, Matthew D., Willson, Tracy A., Wakefield, Matthew J., Trounson, Evelyn, Hilton, Douglas J., Blewitt, Marnie E., Oshlack, Alicia, Majewski, Ian J.
Publicado 2011

SMCHD1's ubiquitin-like domain is required for N-terminal dimerization and chromatin localization

por Gurzau, Alexandra D., Horne, Christopher R., Mok, Yee-Foong, Iminitoff, Megan, Willson, Tracy A., Young, Samuel N., Blewitt, Marnie E., Murphy, James M.
Publicado 2021

Using long-read sequencing to detect imprinted DNA methylation

por Gigante, Scott, Gouil, Quentin, Lucattini, Alexis, Keniry, Andrew, Beck, Tamara, Tinning, Matthew, Gordon, Lavinia, Woodruff, Chris, Speed, Terence P, Blewitt, Marnie E, Ritchie, Matthew E
Publicado 2019

Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation

por Wanigasuriya, Iromi, Kinkel, Sarah A., Beck, Tamara, Roper, Ellise A., Breslin, Kelsey, Lee, Heather J., Keniry, Andrew, Ritchie, Matthew E., Blewitt, Marnie E., Gouil, Quentin
Publicado 2022

Repression of Igf1 expression by Ezh2 prevents basal cell differentiation in the developing lung

por Galvis, Laura A., Holik, Aliaksei Z., Short, Kieran M., Pasquet, Julie, Lun, Aaron T. L., Blewitt, Marnie E., Smyth, Ian M., Ritchie, Matthew E., Asselin-Labat, Marie-Liesse
Publicado 2015

Why weight? Modelling sample and observational level variability improves power in RNA-seq analyses

por Liu, Ruijie, Holik, Aliaksei Z., Su, Shian, Jansz, Natasha, Chen, Kelan, Leong, Huei San, Blewitt, Marnie E., Asselin-Labat, Marie-Liesse, Smyth, Gordon K., Ritchie, Matthew E.
Publicado 2015

edgeR: a versatile tool for the analysis of shRNA-seq and CRISPR-Cas9 genetic screens

por Dai, Zhiyin, Sheridan, Julie M., Gearing, Linden J., Moore, Darcy L., Su, Shian, Wormald, Sam, Wilcox, Stephen, O'Connor, Liam, Dickins, Ross A., Blewitt, Marnie E., Ritchie, Matthew E.
Publicado 2014