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By comparing transcriptomes of multiple organs, physiological functions in different organs can be further explored.
We then identified specific genes expressed in porcine ICM cells by comparing transcriptomes of pure TE and ICMTE in pig normal embryos.
By comparing transcriptomes of C. albicans and H. capsulatum with our data, we found very little overlap and no conserved biological processes.
Digital expression analysis by comparing transcriptomes of two sex-type flowers provided some novel insights into the molecular mechanisms of cucumber sex determination, as well as a rich list of candidate genes for further functional analysis.
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Using DEseq2 analyzing package, by comparing transcriptome of Prom1+/Egfr+ cells from 1-mth-old mouse EZ-SEZ/SVZ to that of in 24-mths-old mice (Fig. 6A), we found a total of 141 age-dependent genes.
We hypothesize that the meiosis-specific genes can be identified by comparing transcriptome profiles of meiocytes and anthers with seedling controls.
Recently, by comparing transcriptome changes of 27 different treatments that are known to promote senescence, it was reported that the early pathways for the induction of senescence differ, but later converge into a shared senescence programme [ 35].
For example, by comparing transcriptome data sets of a test organism cultured under various conditions, sets of genes that are commonly co-expressed are predicted to operate in a single metabolic pathway.
Similarly, we found this gene structure in 75%% of class III peroxidase sequences by comparing transcriptome and genome sequences of horseradish (Näätsaari et al. 2014).
By comparing transcriptome profiles using microarray of dAda2b and dAda2bS transgene-carrier dAda2b larvae, we found that dADA2bS expression alone altered specific mRNA levels to different extents.
Male gamete specific genes were identified by comparing transcriptome data covering different stages of the Ectocarpus life cycle and screened for characteristics expected from gamete recognition receptors.
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