Searching journal content for articles similar to Savic et al. 25 (10): 1581.

Displaying results 1-8 of 8
For checked items
  1. ...of high DAP occupancy are factor dependent. Although some of our observations were similar to what has been observed in vitro, our analysis highlights the value in performing ChIP-seq analysis in primary tissue to characterize tissue-specific gene regulation. The DNA-binding proteins we analyzed show...
  2. ...and warrant investigation. We used a CRISPR/Cas9-mediated epitope tagging strategy called CETCH-seq (Savic et al. 2015) in Ishikawa cells, an endometrial adenocarcinoma cell line that exhibits ESR1 genomic binding similar to endometrial tumor samples (Rodriguez et al. 2019a), to model a common ESR1 LBD...
  3. ...transfected eGFP-ELF1 K562 cell lines was constructed and then a standard ChIP-seq experiment was performed. The FLAG-ATF1 data set was generated by CETCh-seq (CRISPR Epitope Tagging ChIP-seq) which introduced the FLAG tag to endogenous locus of ATF1 by CRISPR and then performed a traditional ChIP-seq...
  4. ...patterns of five AP-1 subunits by using CRISPR to introduce a common antibody tag on each subunit. We find limited evidence for strong dimerization preferences between subunits at steady state and find that, under a stimulus, dimerization patterns reflect changes in the transcriptome. Further, our analysis...
  5. ...for 1139 DAPs using both traditional antibody ChIP-seq and epitope-tagged ChIP-seq methods (The ENCODE Project Consortium 2012; The ENCODE Project Consortium et al. 2020; Partridge et al. 2020). The human liver cancer–derived cell line HepG2 currently has the largest number (n = 814) of ENCODE-released ChIP-seq...
  6. ...plots are presented with CRISPR data from Gasperini et al. as the standard with same conventions as A–C. Predictions are based on data from Reed et al. H3K27ac ChIP-seq at 2 h (E), Sanchez-Priego et al. H3K27ac Cut and Run from H1 GABA late (F), and Hiatt et al. ZMYM3 CETCh-seq with R1274W variant using...
  7. ...species should generalize to closely matched cell types in a related species. To assess the viability of cross-species TF binding prediction, we train neural networks to discriminate ChIP-seq peak locations from genomic background and evaluate their performance within and across species. Cross...
  8. ..., they still require 10,000–500,000 cells to identify targets of the TF SPI1 (also known as PU.1). The use of CETCh-seq (CRISPR epitope tagging followed by ChIP-seq) overcomes the need for TF-specific ChIP-grade antibodies, but it does not reduce the required numbers of cells (Savic et al. 2015). DNA adenine...
For checked items

Preprint Server