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Taxonomies based on gene copy number have a number of advantages over gene expression-based classifications.
The biochemical characterization of these enzymes, whose substrate specificity was predicted based on gene copy number and differential expression rather than sequence identity with characterized enzymes, is an important topic for future research.
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Although these subclasses were "discovered" based on gene associated with copy number variation and steadily expressed in vivo and in vitro, it appears that they represent a natural phenotype of melanoma that segregated separately also by unsupervised testing adopting as a platform the complete genome-wide data set.
There were two copies of Ir40a and Ir93a in D. sechellia and D. simulans but only one copy in D. melanogaster based on gene annotation.
The introduction of high-throughput technologies that survey thousands of genes and their products in a single assay, coupled with powerful analytical tools, has opened up new avenues for classifying breast cancer into biologically and clinically distinct groups based on gene expression patterns [ 18, 19] and DNA copy number alterations [ 20].
In previous study real-time PCR was used regularly based on amoA gene copies, but there has been very little concern on the community shifts of ammonia oxidizers in the presence of NIs and UIs (Liu et al. 2015).
Serial dilutions of these positive plasmids served to generate standard curves using quantitative real time PCR (BIO-RAD System, USA), permitting estimations of absolute quantification based on respective gene copies.
In this work we study the relation between codon choice and tRNA abundance in the human genome by correcting relative codon usage for background base composition and using a measure based on tRNA-gene copy numbers as a rough estimate of tRNA abundance.
So far, there has been no proven method to extract the information on gene copy number aberrations based solely on amplicon sequencing.
Data are based on single copy genes (numbers in circles indicate the number of copies found).
Based on the EGFR gene copy number, patients were further classified into two groups, EGFR FISH positive (high polysomy and gene amplification) or EGFR FISH negative (disomy, low trisomy, high trisomy, and low polysomy).
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