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The identification of gene targets for individual miRNAs is key to understanding their function, thus necessitating accurate methods to identify significant mRNA targets.
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Compared with the previous multistep RT-PCR, one-step multiplex RT-PCR with the primers is the more rapid and accurate method to identify the BCR-ABL breakpoints.
However, both immunotherapies have only demonstrated 12%-24.812%-24.8%ve ratesnse rates in patients with head and neck squamous cell carcinoma (HNSCC), demonstrating a need for a more accurate method to identify those who will respond before their therapy.
Studies reported sonohysterography to be the most accurate method to identify and measure a niche [ 5, 6, 8].
Our genome annotation pipeline proved to be a simple and accurate method to identify a large proportion of genuine transcripts.
TimeXNet is a fast and accurate method to identify active gene sub-networks using time-course gene expression profiles.
This is in contrast with several studies, which have without success tried to find an accurate method to identify risk subjects among schoolchildren or adolescents [ 13, 14].
Here, we demonstrate that short-read sequencing of oligo dT -primed doligo dT -primedDNA provides a robust and accurate method to identify differentially transcDNAed regions of the genome.
28 Finally, Iwanicki-Caron et al. recently reported that CEA kinetics is an accurate method to identify disease progression in patients with advanced colorectal cancer.
Computer based sequence similarity searches of the nucleic acid databases are considered to be a more accurate method to identify retrotransposon families and estimate TE content and distribution in rice genome [ 28- 31].
One approach to explore this aspect is through DNaseI HS mapping, which is an accurate method to identify genomic regulatory regions such as promoters, enhancers, and silencers upstream of transcription start sites.
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