Searching journal content for articles similar to Suzuki et al. 11 (10): 1758.

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  1. ...Sorted B cells in the ASC and MBC gates were separately processed for single-cell RNA-seq using the Chromium Next GEM Single-Cell 3′ Reagent kits v3.1 (10x Genomics) according to the manufacturer instructions with modifications: After the GEM-RT cleanup and full-length cDNA amplification step, 50% of the cDNA...
  2. ...with hallmarks of both, a 5′ CAP and a poly(A) tail. It has been reported that the TeloPrime Full-Length cDNA Amplification Kit could selectively synthesize cDNA molecules from mRNAs carrying a 5′ CAP, in complement to the standard PacBio cDNA library preparation protocol that could only selectively synthesize cDNA...
  3. ...create different circRNA isoforms that have different sequences and unequal interaction potentials. The study of circRNA function thus requires knowledge of complete circRNA sequences. Here we describe psirc, a method that can identify full-length circRNA isoforms and quantify their expression levels...
  4. ...assemblies (Supplemental Table S7). We also identified the insertion site for six retroCNVs that had not been resolved through discordant read mapping (Supplemental Table S7). Most of the retroCNVs were full length with respect to the parent genes, with 153/179 (85.5%) containing the entire parental gene...
  5. ...) on the Polaris IFC and single CTO+ & Calcein AM+ & PTPRC− & CD31− cells were selected to capture sites. Finally, single-cell processing was achieved through template-switching mRNA-seq chemistry for full-length cDNA generation and preamplification on IFC. Supplemental Note 5 elaborates the steps involved in m...
  6. ...used high-throughput cDNA sequencing technologies. For example, in the annotation of the Caenorhabditis elegans transcriptome, more than half of the transcript isoforms lack full-length support and instead rely on inference from short reads that do not span the full length of the isoform. We applied...
  7. ...from 5 µg of total RNA using the Ribo-Zero gold kit (Illumina). Depleted mRNA was fragmented and converted to first-strand cDNA using SuperScript III reverse transcriptase (Invitrogen). During the synthesis of second-strand cDNA, dUTP instead of dTTP was incorporated to label the second-strand cDNA. cDNA...
  8. ...The Drosophila Gene Collection: Identification of Putative Full-Length cDNAs for 70% of D. melanogaster Genes Mark Stapleton 1 , 2 , 6 , Guochun Liao 1 , 3 , Peter Brokstein 1 , 3 , Ling Hong 1 , 3 , Piero Carninci 4...
  9. ...Normalization and Subtraction of Cap-Trapper-Selected cDNAs to Prepare Full-Length cDNA Libraries for Rapid Discovery of New Genes Piero Carninci 1 , Yuko Shibata , Norihito Hayatsu , Yuichi Sugahara , Kazuhiro Shibata , Masayoshi Itoh...
  10. ...Inferring Higher Functional Information for RIKEN Mouse Full-Length cDNA Clones With FACTS Takeshi Nagashima 1 , 2 , Diego G. Silva 3 , 4 , Nikolai Petrovsky 3 , 4 , Luis A. Socha 3 , 4 , Harukazu Suzuki 5 , Rintaro Saito 5...
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