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Sharp gray level variations are mapped to positive (white) detail image values.
The detail signal is almost zero at areas of smooth gray level variation and sharp gray level variations are mapped to positive detail signal values (white).
The variations are mapped to proteins translated from longest transcript of CGC genes in COSMIC v68.
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All variations were mapped to all transcript models, which led to multiple annotations for several loci.
The variations were mapped to the respective genes or intergenic regions using the published annotation of the reference genomes Sterne (NC 005945) for 34F2 and its derivatives and Ames Ancestor (NC 007530) for ΔANR and its derivatives by Annotation Miner software (https://sourceforge.net/projects/annotationminer/).net/projects/annotationminer/
For Arabidopsis, 6,250 splicing variations were mapped to 3,909 FL-cDNA clusters containing at least one FL-cDNA reference assemblies.
A total of 11,716 splicing variations were mapped to 5,599 rice clusters containing at least one FL-cDNA reference assembly.
Finally, due to duplications inside individual datasets and between different data sources, more than 450,000 distinct variations were mapped to the human proteome.
All other assemblies in this cluster were compared to this reference gene structure, and the positions of splicing variations were mapped to the CDS, the 5' UTR, or the 3' UTR.
The contour maps illustrate the regions where the sheet resistances of each bubbler pressure variation are mapped.
The geometry variation and spatial strain hardening variation were mapped onto the model.
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