Searching journal content for articles similar to Sharon et al. 24 (10): 1698.

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  1. ...abundance and mapping initiation sites, crucial for identifying promoter regions and TF binding sites. However, RPA is technically demanding, requiring careful probe design and optimization to minimize background noise. Additionally, it is less suitable for high-throughput analysis.Historically microarrays...
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  2. ...,000 designed promoters from a fixed locus in the human To broaden our understanding of human promoters, we designed a library of 15,753 oligonucleotides representing native and synthetic sequences. We included 508 PIC binding regions and 1875 core promoters of coding genes from the human . In addition, we...
  3. ...control (Bulger andGroudine 2011). For example, developmental enhancers can be located at considerable genomic distances from the gene promoters they regulate, often bypassing several promoters located in the intervening DNA sequence to interact with their target genes (Carvajal et al. 2001; Carter et al...
  4. ...shorter than 50 bp. Twenty–base-pair overhangs were added to both 5′ (acattaggacctttgcagca) and 3′ (ATGacagagcagaaagccct) ends of these sequences, again overlapping the CYC1 promoter and HIS3 gene on the p415-pCYC1 plasmid. The library sequences were purchased from CustomArray Inc. as a mixed oligo pool...
  5. ...of library molecules generated from the control oligonucleotide was determined using a probe-based qPCR assay specific to successfully converted oligonucleotides. Note that no selection is necessary on the P7 adapter sequence, as molecules without P7 adapters lack the biotin required for bead binding...
  6. ...) in HPF1 for NA and WA alleles. Hatched rectangle: a HPF1 internal unique region with high sequence variation between NA and WA alleles. Right: repeat motif units. Amino acids are colored according to the RasMol nomenclature. Numbers = motif size (amino acids). (B) Size variation of genes containing long...
  7. ...Prioritizing molecular alterations that act as drivers of cancer remains a crucial bottleneck in therapeutic development. Here we introduce HIT’nDRIVE, a computational method that integrates genomic and transcriptomic data to identify a set of patient-specific, sequence-altered genes, with sufficient...
  8. ...A, Segal E. 2012. Inferring gene regulatory logic from high-throughput measurements of thousands of systematically designed promoters. Nat Biotechnol 30: 521–530. ↵Sharon E, van Dijk D, Kalma Y, Keren L, Manor O, Yakhini Z, Segal E. 2014. Probing the effect of promoters on noise in gene expression...
  9. ...chosen by Vega pseudogene designation or lack of nearby RefGene Olfr annotation. Mouse olfactory receptor promoters Genome Research 1251 www..org understand the evolutionary or regulatory significance of the use of promoter sequences with extreme AT content, we constructed a secondary promoter data set...
  10. ...devoted to mapping TF networks. In Saccharomyces cerevisiae, protein–DNA interactions have been identified for most TFs by ChIP-chip, and expression profiling has been done on strains deleted for most TFs. These studies revealed that there is little overlap between the genes whose promoters are bound...
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