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We then analyzed gene expression profiles in the treated cells using a cDNA microarray consisting of 18,432 genes.
A DNA microarray consisting of 221 genes with 390 oligonucleotide probes was designed to identify characteristic genes or gene alleles of S. aureus.
A total of 17,329 S. mansoni DNA sequences were used to design a microarray consisting of 7335 parasite elements or approximately 50% of this parasite's transcriptome.
The impact of substrates for probe immobilization was studied using a microbial diagnostic microarray consisting of probes designed against the pmoA genes of methanotrophs and functionally related bacteria.
A microarray consisting of oligonucleotide probes targeting variable regions of the 16S rRNA gene was designed and tested for the investigation of microbial communities in compost.
A 4 × 44 K 60-mer oligo microarray consisting of 43,833 probes covering 42,440 unigene sequences and 1417 positive and negative Agilent control sequences was designed and used to analyze the expression profiles of four tea plant clones.
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The microarray consisted of a 4 × 4 matrix, including the five pathogen-related antigens and human IgG positive control in duplicate (Fig. 2).
The microarray consisted of overlapping 25mer oligonucleotides tiled on both strands of intergenic regions within the MGAS2221 genome.
The microarray consisted of 3,582 oligonucleotides (70-mer) and covered 94% of 3,816 ORFs of Tohama I, the strain of which the genome has been sequenced [1].
This microarray consisted of 60-mer DNA probes for 470 human miRNAs, sourced from the Sanger miRBase public database (Release 9.1).
The microarray consisted of >300 recombinant Burkholderia proteins and controls.
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