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This facility provides service and support for high data content genomic technologies including Next-Generation Sequencing, Microarrays, and Quantitative PCR.
Transcriptional changes were analyzed using microarrays and quantitative reverse transcription polymerase chain reaction.
We are using microarrays and quantitative RT-PCR using meiotic RNA from wild type and am1 mutants to identify genes that are regulated by AM1.
We hypothesized that gene expression profiles would identify potential mechanisms of toxicity and used DNA microarrays and quantitative real-time PCR (qPCR) to generate profiles.
Further, genomic technologies such as microarrays and quantitative and exquisitely sensitive techniques such as real‐time quantitative polymerase chain reaction have made it possible to reliably generate millions of data points per experiment.
Progress in the application of high-throughput genomic and proteomic analytical tools, such as microarrays and quantitative proteomic technologies has had a positive impact on our understanding of various aspects of maternal communication with gametes and embryos.
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Monocyte transcripts were analyzed by microarray and quantitative PCR.
Liver biopsies were obtained for microarray and quantitative real-time PCR analyses of gene expression.
Treatment-induced changes in gene expression were investigated by microarray and quantitative polymerase chain reaction.Bioluminescence imaging permitted real time longitudinal tracking of grafted human neural stem cells.
We used a custom-designed microarray and quantitative PCR to characterize the rapid transcriptional response to long-term sensitization training in the marine mollusk Aplysia californica.
Using MAGEX microarray and quantitative real time polymerase chain reaction transcript analyses, AgNP-induced disruptiof ofiveve TH-responsive targets was observed.
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