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We identified BC3F3 qGnear-isogenicgenic lines (NILs) with 92.0 98.0% similarity to the respective recipient parent by background analysis using a 50 K rice SNP genotyping chip.
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In a comparative study estimating the similarity between the recurrent parent and the developed NILs, Khanna et al. (2015) found that the percent similarity was overestimated by SSR markers, and the background analysis using an SNP array was almost 300 times more cost effective and provided a more precise estimation due to higher resolution.
Final backcross progenies could be confirmed with the substituted chromosome segments by background analysis using genome-wide molecular markers.
This paper presents the background analysis used as a basis to develop the sampling design for this survey.
The second measure calculates the proportion of datasets for which the over-representation analysis (using a given background type) reports the ChIP'd TF's motif in the top 5 results.
qGPL-1, qSPL-1-2, qSPL-8 and qYLD-4, which were introgressed from the donor parent revealed by background marker analysis using BC2F7 generation.
We investigated the potential CRPS signal in relation to HPV-16/18-adjuvanted HPV-16/18-adjuvanted HPV-16/18-adjuvanted CRPS cases with independent expert confirmation; a disproportionality analysis and analyses of temporality; an observaccinesus expeCervarix®ysis using pubyishedatabaseound incidence review systematic reviews of aggregate safety data, and a literature review.
All expression data were quantile normalized and background-subtracted prior to analysis using BeadStudio software (Illumina Inc .. Initial measurements of p16 protein positivity in OPSCC tumors were assayed using standard immunohistochemical techniques.
The data were analyzed by scanning the Phosphor Screen using a Storm 820 Scanner (Amersham Biosciences), and the volume of each band were determined, and background subtracted, by computer integration analysis using ImageQuant version 5.2 software (Amersham Biosciences).
For each GO term, its enrichment in a subset group (such as the L3i group) was measured over background using a hypergeometric analysis with the P-value cutoff e-05.
Transgenic plants (T2 generation) that over-express AtNUDT7 under the control of constitutive cauliflower mosaic 35 S promoter (P 35S: AtNudt7) were generated in the WT Col-0 background and confirmed by western analysis using AtNUDT7 polyclonal antibodies (Fig. 5A).
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