Searching journal content for articles similar to Gracia et al. 7 (2): 100.

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  1. ...Cell-type- and chromosome-specific chromatin landscapes and DNA replication programs of Drosophila testis tumor stem cell–like cells Jennifer A. Urban1, Daniel Ringwalt1, John M. Urban2,3, Wingel Xue1,5, Ryan Gleason1, Keji Zhao4 and Xin Chen1,2 1Department of Biology, The Johns Hopkins University...
  2. .... These stable chromosome-specific telomere lengths may be explained by slow clonal variation or may represent a new biological mechanism that maintains equilibrium unique to each chromosome end. We examined the role of RIF1 and TEL1 in telomere length regulation and found that TEL1 is epistatic to RIF1 at most...
  3. ..., we perform capture STARR-sequencing of over 70,000 candidate regions to identify active enhancers in primary human neural progenitor cells (phNPCs). We select candidate regions by integrating data from NPCs, prefrontal cortex, developmental timepoints, and GWASs. Over 8000 regions demonstrate...
  4. ...and cDNA sequencing, based on patient-derived DNA and RNA, to systematically evaluate deep intronic variation. We identified all variants across the full genomic loci of targeted genes, applied the in silico tools SpliceAI and Pangolin to predict variants of functional consequence, and then carried out...
  5. ...for capturing chromatin histone modification signatures across tissue sections by taking advantage of a double-barcoded DNA arrays design compatible with in situ Protein A–transposase Tn5 tagmentation. This approach has been validated in presence of fresh-frozen mouse brain tissues but also in decalcified...
  6. ...expression and 10x Genomics multiome combines transcriptome with chromatin accessibility data (Stoeckius et al. 2017). Our single-cell Rapid Capture Hybridization sequencing (scRaCH-seq) method enables the capture of multiple transcripts from preindexed and stored cDNA independent of the 10x Genomics kit...
  7. ...a new short-read Illumina protocol. Because all general purpose RNA-seq protocols struggle to capture the ends of transcripts, we developed Smar2C2, which is a hybrid of the Smart-seq2 and R2C2 methods that tagments not cDNA molecules but the cDNA concatemers generated as part of the R2C2 method (Fig. 1...
  8. ...milieu. However, antibody availability and reliability can be problematic, whereas epitope tagging can be impractical in many cases. To address these limitations, the Protein Capture Reagents Program (PCRP) generated over a thousand renewable monoclonal antibodies (mAbs) against human presumptive...
  9. ...et al. 2016), and this enables the study of cells in the tumor microenvironment with clinical samples.ResultsThe Smart-3SEQ methodPrevious single-cell RNA-seq protocols, Smart-seq (Ramsköld et al. 2012) and Smart-seq2 (Picelli et al. 2013), generate cDNA libraries by the SMART method (Zhu et al. 2001...
  10. ...mimosarum (Sanggaard et al. 2014) and Stegodyphus dumicola (Liu et al. 2019), whereas it was not detected in other arachnid, pancrustacean, or myriapod s (Fig. 1A). We then asked whether CopiaMBDs in Strigamia and Stegodyphus evolved through recruiting MBDs independently or whether the MBD capture occurred...
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