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Weights of tissues were determined for the homogenized samples to provide a denominator for viable count and cytokine level data.
We used a polyclonal-FITC-based immunofluorescence microscopic assay (Pab-IFA) on clinical samples to provide a rapid presumptive diagnosis.
An approximately 80 nm Al overlayer was deposited by sputtering on the surface of the samples to provide a thermal transducer layer for laser pump probe experiments.
> -wrap-foot> *Descrined in adult tumor samples To provide a comprehensive landscape of somatic genomic alterations (termed mutational signatures) in cancer genomes, numerous cancers have been profiled by DNA sequencing [ 2, 34, 45].
We performed microarray analyses with AFAS probes by using oligo-dT and random primed target samples to provide a comprehensive approach for the detection of novel non-poly-adenylated transcripts in the antisense transcriptome.
Conversion of mapped and assembled read counts into normalized digital transcript levels (Fragments Per Kilobase of exon per Million fragments mapped (FPKM)) is a prerequisite for comparing expression profiles of genes within or between samples to provide a comprehensive overview of transcriptomes.
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Hence, it takes a lot more samples to provide an accurate representation of this latter distribution, and the algorithm will suffer from cycle-slip-like phenomena [20].
In addition, Scanning Electron Microscopy (SEM) was conducted to examine the microstructure of some samples to provide an idea about the bond strength between cement and aggregate and identify potential weak points within the mix.
We plotted the raw unrounded copy number estimates on a histogram for all samples to provide an overall assessment on the quality of the data.
These can then be averaged over the complete run of samples to provide an overall confidence that this particular formula is present in the data.
The total RNA of each individual tissue were also sequenced as single component samples to provide an expression signature for each tissue.
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