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  1. ..., a representative set of DMR was sequenced in both strains before subsequent analysis by MALDI-TOF MS of bisulfite treated DNA. (For information on sequences and primers see Supplemental Fig. S2 and Supplemental Table S3, respectively.) DNA sequencing indicated that DMR were often associated with strain...
  2. ...to bisulfite-converted genomic DNA. An allele-specific primer extension step was then carried out; ASOs were extended only if their 3′-base was complementary to their cognate CpG site in the gDNA template. Allele-specific extension was followed by ligation of the extended ASOs to their corresponding LSOs...
  3. ...be beneficial to generate high-density genotyping data in parallel with full sequence. Alternatively, complete allele dropout can be virtually eliminated by a redundant design of LR-PCR primers. It is highly unlikely that two independent sets of primers would both contain SNPs, and so—assuming complete allele...
  4. ...cells. For genotyping we used the HumanNS-12 BeadChips which are based on the Infinium I assay, which avoids PCR-amplification for sample treatment and uses robust allele-specific primer extension of biotinylated dNTPs for discrimination of the two SNP alleles ( Gunderson et al. 2005 ). Both alleles...
  5. ...in Figure 1 . First, total RNA is converted to cDNA using biotinylated primers (both oligo-d(T)18 and random hexamers). The biotinylated cDNA is then attached to a streptavidin solid support and assay oligonucleotides are annealed to their target sequences in the cDNA. A pair of oligonucleotides is annealed...
  6. ...clones (D. Peterson, A. Nagel, S. Wessler, and A. Paterson, unpubl.). The use of ssDNA fractions in cloning would be advantageous in instances where the quantity of genomic DNA is limited. Additionally, fewer base pair mismatches would be expected if primer extension techniques rather than strand...
  7. ...utilizedto investigate the genetic causes of complex human diseases. Here we present a high-throughput genotyping platform that uses a one-primer assay to genotype over 10,000 SNPs per individual on a single oligonucleotide array. This approach uses restriction digestion to fractionate the genome, followed...
  8. ...method that uses a small number of oligonucleotide primers, coupled to allele discrimination on synthetic DNA microarrays. The method (whole- sampling assay, or WGSA) uses a simple restriction enzyme digestion, followed by linker-ligation of a common adaptor sequence to every fragment, allowing multiple...
  9. ...genotyping ( Pastinen et al. 2000 ). Array of Light The genotyping system developed by groups at the National Public Health Institute of Finland and Uppsala University uses allele-specific oligonucleotides on microarrays as templates for primer extension-based genotyping (Figure 1 A). The technique, derived...
  10. ...for specific, high-throughput genotyping by allele-specific primer extension on microarrays. Genome Res. 10 : 1031 – 1042 . ↵ Pollak E.S. , Hung H.L. , Godin W. , Overton G.C. , High K.A. ( 1996 ) Functional characterization of the human factor VII 5′-flanking region. J. Biol. Chem. 271 : 1738 – 1747...
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