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  1. ...(G) primer presenting a known adapter sequence at its 5′-extremity (Adpt1), followed by Klenow polymerase extension (Fig. 1E). Finally, DNA arrays are exposed again to alkaline conditions for releasing the elongated complementary DNA sequence and are collected in a tube for performing two rounds of PCR...
  2. ...for probes (Bio-Rad), final concentration of 900 μmol/L of each primer, and 250 nmol/L of the DNA probe. The ddPCR thermal profile consisted of an initial incubation for 30 min at 37°C followed by the denaturation step for 10 min at 95°C . It was further followed by 45 cycles of amplification, with each...
  3. ...labels (Alloghani et al. 2020). Classification models return categorical variables as the final output (e.g., a pregnancy involving a normal or trisomic fetus), whereas regression models return continuous variables (e.g., fetal DNA fraction in maternal plasma). On the other hand, unsupervised learning...
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  4. ...of the kidney; therefore, we used WTA to spatially profile the transcriptomes of three nephron substructures: the glomeruli, the proximal convoluted tubules, and the distal convoluted tubules.We profiled three normal and four DKD FFPE human kidney samples labeled with fluorescent antibodies targeting epithelia...
  5. ...Phenotypic profiling of the human genome reveals gene products involved in plasma membrane targeting of SRC kinases Julia Ritzerfeld 1 , Steffen Remmele 2 , Tao Wang 1 , Koen Temmerman 1 , Britta Brügger 1 , Sabine Wegehingel 1...
  6. ...can be uti- lized as a versatile mechanism for enzy- matically labeling various types of DNA molecules. Sequencing fragments can be labeled internally, thus obviating the need for fluorescent primers. PCR prod- ucts, such as short tandem repeat poly- morphisms (STRPs), and restriction frag- ments can...
  7. ...at 95°C, followed by 24 cycles of amplification for 15 sec at 95°C and for 4 min at 60°C. The STA product was then diluted 1:6 using DNA suspension buffer (Teknova). Finally, 2.7 mL of the single-cell target amplified DNA was interrogated by Q-PCR for each DNA target of interest using the 96.96 dynamic...
  8. ...or the Illumina Total Stranded RNA Library kit, as per the manufacturer’s instructions. MethylCseq libraries were generated by ligation of methylated sequencing adapters to fragmented genomic DNA, followed by gel purification, sodium bisulfite conversion, and six cycles of PCR amplification. TAB-seq libraries...
  9. .... After PCR, a thermal melt profile was performed to examine the homogeneity of PCR amplicons. Each DNA sample was analyzed in duplicate, and the mean was used for further analysis. The difference of the threshold cycle number (the C t -values) between the methylated and unmethylated alleles, Δ C t = C t...
  10. ...DNA Mapping Using Microfluidic Stretching and Single-Molecule Detection of Fluorescent Site-Specific Tags Eugene Y. Chan 1 , 4 , Nuno M. Goncalves 1 , Rebecca A. Haeusler 1 , Amie J. Hatch 1 , Jonathan W. Larson 1 , Anthony M. Maletta...
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