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Like many computational methods, CENTIPEDE [ 19], based on a hierarchical Bayesian mixture model, requires position weight matrices of known TF binding motifs; therefore, its ability is dependent on the availability of TF binding motifs.
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where, ({boldsymbol {A} :mathbb {R}^{M} mapsto mathbb {R}^{N}} ) is a matrix of known parameters that represents a rendering process.
Specifically, each smooth function has an associated penalty (boldsymbol {nu }_{j}^{sf {T}} mathbf {Q}_{j} boldsymbol {nu }_{j}), where (boldsymbol {nu }_{j}^{sf {T}}=(nu _{j1},ldots,nu _{{jK}_{j}})) and Q j is a positive semi definite square matrix of known coefficients measuring the roughness of the jth smooth component.
The model is as follows: where X i = Z i X i is the appropriate (n i x p) matrix of known covariates with fixed effects β and subject-specific effects b i and ε i in an n i-dimentional vector of residual components.
As p63 binding alone does not explain epidermal gene expression, we searched for potential p63 co-regulators by transcription factor motif enrichment analysis using position weight matrices (PWM) of known transcription factor family motifs (threshold, P-value = 0.01, 1.5-fold enrichment versus background) [ 35].
The output was matched with the most likely TFBS using the MatInspector program Release 7.7.3.1 comprised of a large library and matrix description of known plant-specific cis-elements and their cognate regulators.
Given two sets of PFMs, one comprising the predicted matrices and the other a database of known matrices for TFBSs, a Perl [ 43] script was used to carry out matrix comparisons – comparing each predicted matrix to all the entries in the database.
Predicted TF binding sites on human promoters from ChIP-seq data in conjunction with position weight matrix (PWM) searches of known motifs were mutated to assess their function using luciferase reporter assays in four different immortalized human cell lines.
The oligonucleotides sequences (probe and primers) were specific for matrix gene region of known European swine influenza A viruses, as well as any swine infections that may be due to A (H1N1) pdm-like-2009 influenza A virus.
Pesticide residues extracted from comb samples were quantified using matrix matched calibration standards of known concentrations prepared from neat standard reference material.
In addition, we have identified non-coding RNA genes and differentially expressed transcript isoforms of known matrix components with ageing which require further investigation.
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