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A comprehensive survey of transcriptomes by transcript or its tag sampling, followed by extensive microarray experiments for repeated measurements under various physiological conditions should be able to significantly accelerate de novo analyses and functional annotations of unknown transcriptomes, especially when the genome sequence of the targeted organism is available.
Intensive transcriptome sequencing for the identification of unknown transcript, followed by extensive microarray experiments under various biological contexts, will give us a great opportunity to precisely define cell-specific human transcriptome in the near future.
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The small number of these genes, despite the extensive replication of the microarray experiments, is consistent with previous results that suggest imprinting is rare in adult female Drosophila melanogaster (Coolon et al. 2012; Wittkopp et al. 2006).
We performed extensive analysis on 3 PD microarray experiments available through GEO and found that the RNA splicing gene SRRM2 (or SRm300), sereine/arginine repetitive matrix 2, was the only gene differentially upregulated among all the three PD experiments.
The MAQC datasets were collected in microarray experiments followed by extensive independent quantification of targets using a StaRT-PCR (Standardized Reverse Transcription PCR) approach.
In microarray experiments, we and others found rd1 degeneration to be accompanied by extensive changes in gene expression.
assisted in the microarray experiments.
Comparison of real-time RT-PCR and microarray experiments.
Microarray experiments were conducted according to the manufacturer's instructions.
I.F.K., H.-S.H. and A.M.M. performed microarray experiments.
Parkinson, H. et al. ArrayExpress a public database of microarray experiments and gene expression profiles.
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