Exact(2)
Will timing or sequencing enable us to "have it all"?
If so, can whole genome sequencing enable us to identify which SNPs define each major clade?
Similar(58)
Our novel methodology for WGA and MP sequencing enabled us to accurately define large genomic aberrations using algorithms developed in our laboratory.
This, combined with our PELE analysis that identifies and eliminates errors introduced during sequencing, enabled us to screen a library of over 9,000 individuals using only 32 barcodes.
The use of leptospiral rrs DNA amplification and subsequent sequencing enabled us to detect leptospiral DNA (pathogenic and intermediate clusters) and rule out false-positive reactions.
Such abundant read sequencing enabled us to obtain almost full-coverage contig sequences for the viral segments using de novo assembly, suggesting the importance of this result in terms of being able to evaluate uncharacterized emerging infectious agents using an unbiased sequencing technique at the outbreak of a pandemic.
One of these new techniques, whole genome sequencing, enables us to read an individual's entire genetic code and compare the codes across different individuals.
Exome sequencing enables us to obtain information on functionally important coding regions.
Our sequencing enabled us to assemble and annotate the genomic sequence of the intact chimpanzee NANOG gene [GenBank: DQ179631].
Using SOLiD sequencing enabled us to obtain approximately 100X coverage with 35-nt reads among four genomes.
Here, transcriptome sequencing enabled us to identify putative lateral gene transfers between bacteria and insects including ankyrin-repeat related proteins, lysozyme, and mannanase.
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