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X-ray photoelectron spectroscopy (XPS) provides intermolecular bonding energy to confirm the surface modifications at each step.
With modifications at each stage of the process, it could be applied for other objectives, such as business decisions, policy implications, or innovation program management, and it could include data relevant to government and university relational capital.
The sequences of these inhibitors are the exact antisense copy of the mature miRNAs and all the nucleotides in the inhibitors contain 2'-OMe modifications at each base.
We immunoprecipitated chromatin modified by trimethylation of lysines 4 and 27 and acetylation of lysine 9 of histone H3 (H3K27Me3 H3K27Me3 and H3K9Ac respectively), and used qPCR directed at regions around the gene promoter to identify the chromatin modifications at each promoter.
Subsequently, we defined a modification vector as the vector with binary scores of modifications at each position.
Our method calculates a similarity score between a vector of epigenetic modifications at each position and the feature vector of a focal epigenetic state, such as K27HMD, and outputs the set of regions with the highest sum of similarity scores.
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Analysis of deconvoluted C1s peak in XPS spectra confirmed surface chemical modification at each functionalization step.
In order to allow clustering of sites displaying significant evidence of ASHM by their histone-modification patterns, we calculated the degree of allelic imbalance for each individual modification at each site using a binomial test.
Each of the resulting P-values for each modification at each site were then log-transformed, and sites clustered by their squared Pearson's correlation coefficient using the R statistical package [ 50].
Analysis was performed on three to ten fetal testes from three to six different litters for each modification at each time point and representative images captured as specified below.
The resulting mass lists were further assigned on the basis of the protein sequence of Ub with or without the diglycine (GG) modification at each lysine residue using tolerances of 10 and 20 ppm for precursor and fragment ions, respectively.
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