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  1. ..., State University of New York at Stony Brook 11794, USA. Abstract Many groups have now published data based on the in situ detection of PCR-amplified DNA and cDNA. As with standard in situ hybridization or PCR, variables that can affect in situ PCR results include type of fixative and time of fixation...
  2. ...of different variables for optimizing in situ detection of PCR-amplified DNA. PCR Methods Applic. 2 : 305 – 312 . 7.. Nuovo, G.J., , Becker, J. , MacConnell, P. , Margiotta, M. , Comite, S. , Hochman. H. Nuovo, G.J., Becker, J. MacConnell, P. Margiotta, M. Comite, S. and Hochman. H. 1992 . Histological...
  3. ...previously believed, and deeper sequencing is necessary to detect all active promoters in a given tissue. Here, we present a new method for high-throughput sequencing of 5′ cDNA tags—DeepCAGE: merging the Cap Analysis of Gene Expression method with ultra-high-throughput sequence technology. We apply Deep...
  4. ...). Briefly, a custom oligonucleotide probe pool was designed to capture ESR1 binding regions from both clinical breast tumors and T-47D cell line ESR1 ChIP-seq. Pooled human genomic DNA was sheared, captured, PCR-amplified, and cloned into the hSTARR-ORI plasmid (Addgene, plasmid 99296). The ESR1-focused...
  5. ...(c.1181G>C, p.R394T), previously identified as a potential mechanism of resistance to T-DXd, because SLX4 encodes a DNA repair protein that regulates structure-specific endonucleases and seems to play a role in resistance to TOP1 inhibition. Among HER2- cell lines, MCF-7 and ZR-75-1 (HR+) and MDA...
  6. ...selection and massively parallel bisulfite sequencing to profile DNA methylation in genomic regions spanning hundreds of thousands of bases. This single molecule strategy enables methylation variable positions to be quantitatively examined with high sampling precision. Using bisulfite capture, we assessed...
  7. ...the Smart-seq2) to add a PCR sequence at the cDNA 3′ end, after which the cDNA was PCR-amplified and fragmented with Tn5A transposase. The fragmented cDNAs were then amplified to generate the sequencing library (as shown in Fig. 2A; Supplemental Fig. 2).View larger version: In this window In a new window...
  8. ...levels of read numbers and accuracy, and many, like standard RNA-seq, ChIP-seq, or targeted sequencing of PCR amplified genomic DNA, are unlikely to ever take advantage of the raw read length ONT and PacBio sequencers provide. However, there have been several studies to take advantage of long...
  9. ...-restricted satellite DNA and DNA transposon fragments occupy its terminal ends. We infer that D. biarmipes relies instead on a recombination-based mechanism conserved from yeast to flies to humans. Telomeric retrotransposon diversification and disappearance suggest that persistently “selfish” machinery shapes telomere...
  10. ...coaccessibility framework, Cicero, which identified 146,818 links between promoters and putative distal regulatory DNA. Identified coaccessibility networks showed cell-type specificity, shedding light on key dynamic loci that reconfigure to specify hippocampal cell lineages. Lastly, we performed an additional sci...
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