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We have used a mixed-genome microarray to perform comparative-genome analysis of 257 strains from this collection.
To identify genes preferentially expressed in the AZ of tomato flower pedicels at anthesis, we used the Agilent tomato 44K oligonucleotide DNA microarray to perform transcriptome assays comparing AZs and the non-AZ pedicel regions, Dis and Prox.
To date, the most popular application of RNAseq technology is mRNA sequencing because most researchers use RNAseq as a replacement for microarray to perform high throughput gene expression profiling [ 3– 6] and coding regions remain the focus of human disease research.
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We have demonstrated that molecular bar-codes designed for S. cerevisiae are transferable to E. coli, and that they can be used with pre-existing microarrays to perform competitive growth experiments.
The second approach used whole genome microarrays to perform a differential expression profiling experiment.
Here, we used microarrays to perform systematic profiling of human miRNAs in plasma from NPC patients.
To further examine possible disturbance of gene expression in the Pygo1/ Pygo2 mutant kidneys, we used microarrays to perform a global analysis of gene expression changes.
In this study we employ DNA microarrays to perform a genome-wide transcriptome profiling of a S. coelicolor afsS disruption mutant.
We used Affymetrix oligonucleotide microarrays to perform a detailed transcript analysis on the mechanism of controlled involution after withdrawal of the pups at day seven of lactation.
We utilised SNP microarrays to perform high-resolution genome-wide combined LOH and copy number screening of 21 primary stage T1 tumors.
To investigate potential molecular mechanisms leading to the changes observed in muscle physiology in the absence of RIP140, we used Affymetrix microarrays to perform expression profiling on RNA isolated from the gastrocnemius of WT and RIP140 null mice.
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