Searching journal content for articles similar to Brusic et al. 13 (6b): 1307.

Displaying results 1-10 of 5923
For checked items
  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. ...′ GTACTCTGCGTTGATACCACTGCTT). The two cDNA primer sets differ only in the 5′ end, while the segments for the 3′ end are the same. TeloPrime-based kit V2 includes updated reaction conditions in comparison with kit V1, while the method of cDNA generation remains unchanged. For each protocol, we used 1 μg homogeneous RNA...
  3. ...using HiSeq 4000 PE150 (50 million to 100 million reads per library).Long-read Frac-seqFrom the same fractionated mRNA used prior for Illumina sequencing, full-length cDNA was prepared using the rolling circle amplification to concatemeric consensus (R2C2) method (Volden et al. 2018). Libraries were...
  4. ...in quantifying expression levels. First, we used the data set of human fetal samples mentioned above, which also included the expression levels of some BSJs independently measured by RT-qPCR (Szabo et al. 2015). We applied psirc to deduce the expression level of each full-length circRNA isoform using the RNA...
  5. ...landscape of canid retroCNVs has not been characterized. Here, retroCNV discovery was performed on a whole- sequencing data set of 293 canids from 76 breeds. We identified retroCNV parent genes via the presence of mRNA-specific 30-mers, and then identified retroCNV insertion sites through discordant read...
  6. ...) 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...
  7. ...,000,000 full-length cDNA sequences at a median accuracy of 97.9% using our nanopore sequencing-based Rolling Circle Amplification to Concatemeric Consensus (R2C2) protocol. We used this data set to (1) show that deep and accurate full-length cDNA sequencing can be used to provide isoform-level transcriptome...
  8. ...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...
  9. ..., full-length cDNAs, and RNA sequencing (RNA-seq) of cDNA fragments using massively parallel sequencing (Reboul et al. 2003; Ramani et al. 2011; Uyar et al. 2012; Grün et al. 2014; Boeck et al. 2016; Tourasse et al. 2017). Short RNA-seq reads, typically shorter than 200 nt, have played a leading role...
  10. ...). Comparative DRS analyses of RNA obtained from cells infected with (1) plaque-purified HCoV-229E and (2) newly rescued recombinant HCoV-229E (without prior plaque purification), respectively, would help to address the possible role of prematurely terminated in vitro transcripts produced from full-length cDNA...
For checked items

Preprint Server