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CODING

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 I. (noun) 

Sense 1

Meaning:

Act of writing in code or cipherplay

Synonyms:

coding; cryptography; secret writing; steganography

Classified under:

Nouns denoting acts or actions

Hypernyms ("coding" is a kind of...):

committal to writing; writing (the activity of putting something in written form)

Hyponyms (each of the following is a kind of "coding"):

encoding; encryption (the activity of converting data or information into code)

recoding (converting from one code to another)

decipherment; decoding; decryption (the activity of making clear or converting from code into plain text)

Derivation:

code (convert ordinary language into code)

 II. (verb) 

Sense 1

-ing form of the verb code

Credits

 Context examples: 

The CYP2C19*12 allele exhibits a clinically-relevant SNP (c.1473A>C) in exon 9 that results in a X491C coding change.

(CYP2C19*12 Allele, NCI Thesaurus)

The CYP2C19*3 allele exhibits a clinically-relevant SNP (c.636G>A) in exon 3 that results in a W212X coding change.

(CYP2C19*3 Allele, NCI Thesaurus)

A point mutation in a coding DNA sequence that causes a base change which results in an amino acid change in the protein product.

(Missense Mutation Abnormality, NCI Thesaurus)

A fusion gene that results from a chromosomal translocation t(11;19)(q23;p13.1) which fuses the first 7 exons of the MLL gene to most of the coding sequence of the ELL gene.

(MLL/ELL Fusion Gene, NCI Thesaurus)

A fusion gene that results from a chromosomal translocation t(X;2)(q11;p23) which fuses most of the coding sequence of the MSN gene with the 3' portion of the ALK gene.

(MSN/ALK Fusion Gene, NCI Thesaurus)

A character string that is a revision of the original text to enable the coding of the text.

(Name Code Modified Text, NCI Thesaurus)

A point mutation occurring within the protein-coding region of a gene, and which codes for a different amino acid than expected.

(Missense Mutation, NCI Thesaurus)

A recombinant fusion protein derived from the coding sequences of two growth factors, interleukin-3 (IL-3) and granulocyte-macrophage colony-stimulating factor (GM-CSF).

(Milodistim, NCI Thesaurus)

The CYP2C19*5 allele exhibits a clinically-relevant SNP (c.1297C>T) in exon 9 that results in a R433W coding change in the heme-binding region of the protein.

(CYP2C19*5 Allele, NCI Thesaurus)

The CYP2C19*6 allele exhibits a clinically-relevant SNP (c.395G>A) in exon 3 that results in a R132Q coding change.

(CYP2C19*6 Allele, NCI Thesaurus)




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