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Gene expression of these genes was tested with a Fisher's Exact Test comparing observed tag counts out of the entire and an unadjusted p-value of 0.05.
The distribution of mutations in 173 muscle disease genes was tested against a null model as follows.
The expression stability of eight candidate reference genes was tested in leaves, roots and callus.
Genetic manipulation of 87 homologous fly genes was tested for modulation of neurotoxicity caused by human Tau, which forms neurofibrillary tangle pathology in AD.
Moreover, the Reactome_PI3K_AKT_activation gene-set, consisting of 38 genes, was tested for its association with ICV (downloaded from http://software.broadinstitute.org/gsea/msigdb/genesets.jsp).jsp
The relationship between specific LMRs with TF-binding motifs and their target genes was tested by adapting the gene set enrichment analysis (GSEA).
Taxonomic specificity for Ascomycota GH28 genes was tested by comparing GH28 composition in leaves to internal transcribed spacer (ITS) amplicon composition using pyrosequencing.
A new technique was developed to produce a multigene methylation signature in each sample, and its potential for selection of informative genes was tested using DNA from formalin-fixed, paraffin-embedded breast cancer tissues.
Expression of cloned genes was tested on plate-assays using AZCL-HE-cellulose containing plates for endoglucanase activity and esculin-containing plates to detect β-glucosidase activity.
In a discovery cohort of 1018 patients, a panel of 90 single-nucleotide polymorphisms (SNPs) in 49 candidate genes was tested with Cox proportional hazard models to identify clinical and genomic multivariate predictors of incident death.
To test whether induction of OsGLP genes by the mock treatment is consistent with response to wounding, a subset of OsGLP genes was tested by RT-PCR in leaf tissue after pressurized water spray and mechanical wounding (Fig. 5).
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