Searching journal content for articles similar to Van Nostrand and Kim 23 (6): 941.

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  1. ...a fosmid construct, or did not pass ChIP-seq metrics after recombineering (Paix et al. 2017; Dokshin et al. 2018; Ghanta and Mello 2020). The CRISPR approach has the advantage of being a single copy and retaining the native regulatory context of the TF gene. To test whether this approach impacted TF...
  2. ...to partition the training set into groups that have distinct RNA-seq read count distributions, and (2) the data set is informative for a large fraction of target genes. We find that Pol II ChIP-seq data meets both requirements. To examine the first requirement, we built a training set for human cell line K562...
  3. ..., affects different uses of ChIP-seq data. All data sets used in the analysis have been deposited for public viewing and downloading at the ENCODE ( http://encodeproject.org/ENCODE/ ) and modENCODE ( http://www.modencode.org/ ) portals. Footnotes ↵ 28 Corresponding authors E-mail mpsnyder...
  4. ...is essential to understand gene regulation. Chromatin immunoprecipitation followed by sequencing (ChIP-seq) provides a global map of the regulatory binding network. Most ChIPseq analysis tools focus on identifying binding regions from coverage enrichment. However, less work has been performed to infer...
  5. ...of the modENCODE Project, we generated deep RNA-seq data sets for C. elegans using a consistent methodology across the life cycle, including a detailed embryonic time course. These data sets provide the community with information about the patterns of protein coding gene and ncRNA expression as well...
  6. ...regulatory regions. To verify that our ATAC-seq data correctly identify regulatory regions throughout the epi, we used multiple histone modification ChIP-seq data sets from modENCODE (Li et al. 2009; Ho et al. 2014) and ChromHMM (Ernst and Kellis 2012) to build predictive models of the epi. Chrom...
  7. ...leaders. By combining this data set with the modERN ChIP-seq resource, we are able to support and predict gene regulatory relationships. The detailed information on differences and similarities between gene expression in cell lineages and tissues should be of great value to the community and provides...
  8. ..., we performed RNA-seq to determine expression levels of all genes and ChIP-seq using an antibody recognizing the unphosphorylated C-terminal repeat of RNA polymerase II (RNA Pol II), which recognized RNA Pol II bound at the TSSs of active genes in gastrulae (Supplemental Fig. S5) and planulae (Figs. 2...
  9. ...the complementarity between physical evidence of regulatory interactions (TF binding, motif conservation) and functional evidence (coordinated expression or chromatin patterns) and demonstrates the power of data integration for network inference and studies of gene regulation at the systems level. Footnotes...
  10. ...in green and orange, respectively) were considered “fragile” or “resistant.” Jeffers and Lieb 76 Genome Research www..org TFBSs. We collected a set of 35,062 TFBSs bound at any stage of C. elegans development, as identified by TF ChIP-seq from the modENCODE Consortium (Araya et al. 2014). The DNA...
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