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  1. ...populations of early human embryonic cells. Cell Stem Cell 16: 135–141. doi:10.1016/j.stem.2015.01.005 ↵Hansen KD, Sabunciyan S, Langmead B, Nagy N, Curley R, Klein G, Klein E, Salamon D, Feinberg AP. 2014. Large-scale hypomethylated blocks associated with Epstein-Barr virus–induced B-cell immortalization...
  2. ...samples: tissues, primary cell lines, embryonic cell lines, and blood leukocytes (Fig. 3A; detailed tree in Supplemental Fig. S8). The blood leukocyte-derived samples, including both peripheral blood leukocytes and Epstein-Barr virus (EBV)-immortalized lymphoblastoid cell lines, clustered together...
  3. ...the described process. Using bisulfite genomic sequencing of multiple clones, we have obtained the DNA methylation status of every CpG dinucleotide in the genome of the Human Papilloma Viruses 16 and 18 and Human Hepatitis B Virus, and in all the transcription start sites of the Epstein-Barr Virus...
  4. ...differences. Using data from oxBS-seq, we were able to identify DMRs by only taking methylation changes into account between normal and matched tumor samples. Identified DMRs were grouped into small-scale DMRs and large-scale blocks according to their length (see Methods). We found that in both liver and lung...
  5. ...-DMRs, corresponding to both hypermethylated regions (48%) and hypomethylated regions (52%) (Fig. 1B; Supplemental Table S2). To independently validate these changes, we generated methylation-sensitive pyrosequencing data on control versus MTB-infected DCs from five new individuals. We targeted 21 CpG sites that were...
  6. ...sets, study design is unlikely to impact large-scale, highly robust trends across species. However, this study design choice is particularly important if one is interested in individual genes (as shown by an example in Fig. 1C).Putatively functional tissue-specific gene expression patternsTo analyze...
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