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In short, write the researchers, "groups of autonomous machines could demonstrate prejudice by simply identifying, copying and learning this behavior from one another".
We manually identified copy number segments worthy of committee discussion and potential classification.
We identified copy number variants (CNVs) with control-FREEC55 based on exome-sequencing data to analyze the copy number state of each tumor.
To determine the association of identified copy number variations (CNVs) in whole genome with the risk of Avellino corneal dystrophy (ACD) in a Korean population.
Genes in the final analysis were merged with methylation data and identified copy number aberration regions according to genomic locations.
We identified copy number change of three loci at 20q11, 1p36 and 6q27 to be significantly associated with CCNE1 amplification in ovarian tumors.
A complete list of all identified copy number aberrations and the mutation status of 7 genes is given for the cell lines showing synergistic behavior in Table S1.
In addition, CMA identified copy number variations (CNVs) of uncertain significance in 262 probands; however, parental studies usually facilitated clinical interpretation.
First three columns – genome coordinates of the identified copies.
Summary of the identified copy-number variants in each of the five Bos taurus breeds.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com