1
Length polymorphisms in the amplified DNA distinguished unrelated strains of all bacteria.
2
The amplified DNA was sequenced and compared with other registered P. ovale isolates.
3
Amplified DNA was detected by gel electrophoresis and slot blot hybridization.
4
Amplified DNA samples were spotted on silane-treated glass slides using a micro array spotter.
5
Two microsatellite fragments were amplified from whole genome amplified DNA.
6
A chemical agent, N-phenacylthiazolium bromide, that cleaves such cross-links made it possible to amplify DNA sequences.
7
A universally primed polymerase chain reaction was developed to amplify DNA dissected from GTG-banded human chromosomes.
8
The amplified DNA was cloned into Escherichia coli.
9
Herein is described a method to amplify DNA when sequence information is available for only one primer.
10
Amplified DNA was directly sequenced and translated to amino acids to analyze PRI-associated major and accessory mutations.
11
Ultra-deep Illumina sequencing was performed on whole genome amplified DNA derived from a Chlamydia trachomatis-positive vaginal swab.
12
The fragmentation process prevented leakage of amplified DNA to neighboring areas as often experienced with in situ PCR.
13
When used in combination, the SLTI and SLTII oligonucleotide primers amplified DNA from all of the SLT-EC tested.
14
The location of the activating mutation was determined by hybridization of amplified DNA to mixed sequence oligonucleotide probes.
15
Polymerase chain reaction- amplified DNA samples from 793 unrelated individuals with hemophilia A were screened by discriminant oligonucleotide hybridization.
16
The low amount of amplified DNA obtained did not allow the sequencing and identification of the species of Leishmania.