Examples of 'nucleotide sequence analysis' in a sentence
Meaning of "nucleotide sequence analysis"
Nucleotide sequence analysis: The process of examining and interpreting a sequence of nucleotides in DNA or RNA to identify genes, regulatory elements, or other genetic information
How to use "nucleotide sequence analysis" in a sentence
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nucleotide sequence analysis
The inserts were subjected to nucleotide sequence analysis.
Nucleotide sequence analysis.
The sequence of the construct is verified by nucleotide sequence analysis.
The differences between nucleotide sequence analysis and protein analysis is unknown.
The resultant plasmid constructs were confirmed by nucleotide sequence analysis.
The plasmid was checked by nucleotide sequence analysis and no artifacts were found.
All resulting rescue support plasmids were verified by nucleotide sequence analysis.
Nucleotide sequence analysis of this region revealed a number of putative transcription factor binding sites.
The identity of the obtained clone was confirmed by nucleotide sequence analysis.
The nucleotide sequence analysis was performed on cDNA isolated from a human prostate cDNA library.
The exact boundaries of the exons were determined by nucleotide sequence analysis.
Nucleotide sequence analysis of cloned PCR product confirmed the sequences spanning the restriction site markers.
Plasmids representing each fragment were submitted for nucleotide sequence analysis.
Nucleotide sequence analysis of genotyping PCR products.
Each of the resultant plasmid constructs was confirmed by nucleotide sequence analysis.
See also
nucleotide reverse transcriptase inhibitors
nucleotide sequence
nucleotide sequence coding
nucleotide sequence encoding
nucleotide sequence
nucleotide sequence coding
nucleotide sequence encoding
Nucleotide sequence analysis of the cloned PCR products followed by BLAST analyses confirmed their identity.
The entire sequence and orientation were confirmed by nucleotide sequence analysis.
Nucleotide sequence analysis of the PCR product revealed FIV Bangston specific sequences.
Plasmid sequences were verified by automated nucleotide sequence analysis using standard protocols.
The nucleotide sequence analysis was carried out in the following manner,.
Resultant recombinant plasmids were used as templates for automated nucleotide sequence analysis.
Nucleotide sequence analysis indicates that the two GluR5 variants are otherwise identical.
Phagemid clones were characterized by restriction enzyme mapping and partial nucleotide sequence analysis.
Nucleotide sequence analysis of pBig-h3a revealed that it contained a partial open reading frame.
Orientation and in frame insertion of ruPAR cDNA was further confirmed by nucleotide sequence analysis.
Nucleotide sequence analysis was carried out as described in Example 1.
These colonies comprising bridge amplification products may then be subjected to nucleotide sequence analysis.
DNA manipulations and nucleotide sequence analysis.
Nucleotide sequence analysis of 11 resulting clones identified seven distinct V genes.
One of these DNA was further characterized by nucleotide sequence analysis.
Nucleotide sequence analysis of the plasmid, however, was not reported.
The number of repeated ARE sequences and their orientation were verified by nucleotide sequence analysis.
Genetic variability of the AIDS virus, nucleotide sequence analysis of two isolates from African patients.
A fragment of maize mtDNA from T cytoplasm was characterized by nucleotide sequence analysis.
Nucleotide sequence analysis was carried out according to the chain termination procedure [ 24 ].
Alternatively, an automated sequencer may be used to perform nucleotide sequence analysis.
The apparatus for nucleotide sequence analysis used was A.L.F.
Example 4 relates to further characterization of cloned genes by nucleotide sequence analysis.
M9, was characterized by nucleotide sequence analysis and subsequently used for the construction of mutant M8.9.
A 20-kb region of pSymA containing the nor-nir genes was delineated by nucleotide sequence analysis.
The SNP 's are selected based on a nucleotide sequence analysis of 100 platelet apheresis donors.
The clone with the longest insert ( AC1 ) was subjected to nucleotide sequence analysis.
Nucleotide sequence analysis of this clone identified it as decay accelerating factor ( DAF, CD55 ).
Inserts from two positive clones, MJ1 and MJ2 were subjected to nucleotide sequence analysis.
Figure 17H to 17L depict nucleotide sequence analysis at the GMD target locus.
The longest one, clone lambda-13, was subjected to nucleotide sequence analysis.
The lambda-13 clone was subjected to nucleotide sequence analysis.
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Examples of using Nucleotide
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