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  1. ...′-sgRNA pair or control EGFP/mCherry sgRNAs Lenti-multi-CRISPR plasmid-transfected cells was purified using a RNeasy kit with an on-column DNase I treatment according to the manufacturer's protocol (Qiagen). RNA was eluted in 25 µL ddH2O, quantified using NanoDrop, and quality-controlled by agarose gel...
  2. ...occupancy adjacent to these binding sites (Fig. 2B). In good agreement, DNase-seq data show a combination of a footprint peak with adjacent oscillation patterns, whereas ATAC-seq detects a peak representative for open chromatin at the CTCF binding sites (Fig. 2B). Our data suggest that short cfDNA most...
  3. ...and chromatin accessibility map across regenerative stages provides new insights into regeneration regulatory mechanisms and serves as a valuable resource for the community.The zebrafish (Danio rerio) serves as an excellent model organism for studying complex tissue regeneration processes owing to its...
  4. ...Examining the dynamics of three-dimensional organization with multitask matrix factorization Da-Inn Lee1 and Sushmita Roy1,2 1Department of Biostatistics and Medical Informatics, University of Wisconsin–Madison, Madison, Wisconsin 53715, USA; 2Wisconsin Institute for Discovery, Madison, Wisconsin...
  5. ...calculation, which was adjusted according to the respective populations. Additionally, we utilized HaploReg to annotate deleterious-associated variants to identify those potentially affecting SHROOM3 expression. Variants situated in enhancer or promoter regions, as indicated by histone or DNase marks in stem...
  6. ...Elasmobranch sequencing reveals evolutionary trends of vertebrate karyotype organization Kazuaki Yamaguchi1,6, Yoshinobu Uno1,7, Mitsutaka Kadota1, Osamu Nishimura1, Ryo Nozu2,8, Kiyomi Murakumo3, Rui Matsumoto3, Keiichi Sato2,3 and Shigehiro Kuraku1,4,5 1Laboratory for Phyloinformatics, RIKEN...
  7. ..., Illinois 60628, USA ↵3 These authors contributed equally to this work. Corresponding author: zhe.ji@northwestern.eduAbstractWe describe a low-input RNase footprinting approach for the rapid quantification of ribosome-protected fragments with as few as 1000 cultured cells. The assay uses a simplified...
  8. ...Suv39h-catalyzed H3K9me3 is critical for euchromatic organization and the maintenance of gene transcription Christine R. Keenan1,2,4,6, Hannah D. Coughlan1,2,4, Nadia Iannarella1, Andres Tapia del Fierro1,2, Andrew Keniry1,2, Timothy M. Johanson1,2, Wing Fuk Chan1,2,7, Alexandra L. Garnham1...
  9. ...along the genome. Compared to methods that require genetically modified histones, our DNase-based approach is easily applied in any organism, which we demonstrate by producing maps in yeast and human. Compared to micrococcal nuclease (MNase)-based methods that map nucleosomes based on cuts in linker...
  10. ...limitations. We have developed a footprinting method to predict TF footprints in active chromatin elements (TRACE) to improve the prediction of TFBS footprints. TRACE incorporates DNase-seq data and PWMs within a multivariate hidden Markov model (HMM) to detect footprint-like regions with matching motifs...
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