Searching journal content for articles similar to Miller et al. 23 (4): 679.

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  1. ...information, and considers most of the interference factors to improve the identification of IpA events (Supplemental Fig. S15). We also compared IPAFinder with APAlyzer, which analyzes intronic polyadenylation by using RNA-seq data based on known poly(A) sites (such as those annotated in the Poly...
  2. ...first (She et al. 2009).To collect transcriptome evidence, we downloaded the RNA-seq data from NCBI's BioProject database (https://www.ncbi.nlm.nih.gov/bioproject/) under accession number PRJNA230881 (tissues include whole embryo, adult gonad, brain, tail, and pooled organs) and mapped them...
  3. ...Ranking noncanonical 5′ splice site usage by -wide RNA-seq analysis and splicing reporter assays Steffen Erkelenz1,4,5, Stephan Theiss2,4, Wolfgang Kaisers3, Johannes Ptok1, Lara Walotka1, Lisa Müller1, Frank Hillebrand1, Anna-Lena Brillen1, Michael Sladek1 and Heiner Schaal1 1Institute of Virology...
  4. .... S10A–C). The lack of reactivity among the monoclonal antibodies highlights the possibility of false-negative results with ELISA-based screening methods since MMR-82 was obviously a positive binder to MeV-F.Germline-specific repertoire analysis of antibody sequences confirm B cell class and allows...
  5. ...short-read RNA-seq as a modularized software that contains chimeric read extraction, fusion transcripts identification, expression quantification, gene fusion annotation, and interactive visualization. To benchmark existing tools, we collected or generated comprehensive simulation data sets to reflect...
  6. ...,000 bases (targeting 20 kb of 2.2 Mb pneumococcal (∼ 1%) in a 0.01 dilution) in a mixed sample. Taken together, these results indicate that targeting CBL for the identification and serotyping of S. pneumoniae is a viable alternative to whole- enrichment in complex microbial samples.View larger version...
  7. ...to knock down genes in cells utilizing small interfering RNA. While unexpected, this functionality is not surprising due to the harnessing of evolutionary tumor selection in forward genetic screens. Pth,Ptprd, andTgfbr1were identifiedonlyafterRNA-seq-based analysis approaches described here, and each gene...
  8. ...it to map two novel ENU-induced cardiovascular mutants, with mutations found in the ctr9 and cds2 genes. MMAPPR can be directly applied to other model organisms, such as Drosophila and Caenorhabditis elegans , that are amenable to both forward genetic screens and pooled RNA-seq experiments. Thus...
  9. ...RNA-seq of 272 gliomas revealed a novel, recurrent PTPRZ1-MET fusion transcript in secondary glioblastomas Zhao-Shi Bao 1 , 2 , 3 , 13 , Hui-Min Chen 4 , 13 , Ming-Yu Yang 4 , 13 , Chuan-Bao Zhang 1 , 2 , 3...
  10. ...and PCR) can achieve relatively high cell throughput, other strategies have been developed that incorporate additional tiers of indexing to increase throughput to even greater levels using ligation-based index addition, similar to what was developed previously for single-cell RNA-seq (Rosenberg et al...
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