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Genomic DNA was characterized using the Affymetrix 250 K Nsp and Sty arrays.
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To test the performance of this instrument, individual biotinylated DNA molecules were assembled between two streptavidin beads, and the DNA elasticity was characterized using both laser trap and flow forces.
DNA polymerase priming bias was characterized using a synthetic library amplification system and NGS.
Activated sludge biofouling was characterized using DNA-based assays.
Species identity of a representative subset of the slugs collected in the third field screen and of the slugs used in the first experiment was characterized using an established DNA barcoding approach, based on DNA sequencing of a polymerase chain reaction (PCR -amplified fragment of the mitochondrial cytochrome c oxidase subunit I gene (COI) [ 23].
Multiplex OLA sensitivity was characterized using template DNA sequences consisting of an abridged subtype B HIV-1 Pol gene consensus and six different permutations of drug resistance mutations.
In the present study, the methylome of H. pylori UM032 was characterized using SMRT DNA sequencing and compared to those of several previously characterized H. pylori strains [ 32, 36].
The novel IGQ-hairpin system was characterized using the p53 gene as the model target DNA.
The organization of C. roseus chromosomes was characterized using several DNA/chromatin staining techniques and FISH of rDNA.
DNA sequences were characterized using the PAO1 genome accessible at http://www.pseudomonas.com.
Novel c0 t-1 DNA sequences were characterized using the EMBL database homology search against nucleotide and amino acid sequences and an e-value threshold of 10-3.
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