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  2. Gene nomenclature - Wikipedia

    en.wikipedia.org/wiki/Gene_nomenclature

    Gene symbols generally are italicised, with all letters in uppercase (e.g., NLGN1, for neuroligin1). Protein designations are the same as the gene symbol, but are not italicised; all letters are in uppercase (NLGN1). mRNAs and cDNAs use the same formatting conventions as the gene symbol. [17]

  3. Nucleic acid notation - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_notation

    Ambigrams (symbols that convey different meaning when viewed in a different orientation) have been designed to mirror structural symmetries found in the DNA double helix. [9] By assigning ambigraphic characters to complementary bases (i.e. guanine: b, cytosine: q, adenine: n, and thymine: u), it is possible to complement DNA sequences by simply ...

  4. Lists of human genes - Wikipedia

    en.wikipedia.org/wiki/Lists_of_human_genes

    NB: Each list page contains 5000 human protein-coding genes, sorted alphanumerically by the HGNC-approved gene symbol. Follow the Python code link for information about updates to the list of genes on these pages.

  5. List of genetic codes - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_codes

    While there is much commonality, different parts of the tree of life use slightly different genetic codes. [1] When translating from genome to protein, the use of the correct genetic code is essential.

  6. GENCODE - Wikipedia

    en.wikipedia.org/wiki/GENCODE

    Also, the GENCODE website contains a Genome Browser for human and mouse where you can reach any genomic region by giving the chromosome number and start-end position (e.g. 22:30,700,000..30,900,000), as well as by ENS transcript id (with/without version), ENS gene id (with/without version) and gene name. The browser is powered by Biodalliance. [19]

  7. Copy number variation - Wikipedia

    en.wikipedia.org/wiki/Copy_number_variation

    Copy number variation was initially thought to occupy an extremely small and negligible portion of the genome through cytogenetic observations. [12] Copy number variations were generally associated only with small tandem repeats or specific genetic disorders, [13] therefore, copy number variations were initially only examined in terms of specific loci.

  8. DNA annotation - Wikipedia

    en.wikipedia.org/wiki/DNA_annotation

    Generalized flowchart of a structural genome annotation pipeline. First, the repetitive regions of an assembled genome are masked by using a repeat library. Then, optionally, the masked sequence is aligned with all the available evidence (ESTs, RNAs, and proteins) of the organism being annotated.

  9. HUGO Gene Nomenclature Committee - Wikipedia

    en.wikipedia.org/wiki/HUGO_Gene_Nomenclature...

    Full gene names, and especially gene abbreviations and symbols, are often not specific to a single gene. A marked example is CAP which can refer to any of 6 different genes (BRD4 Archived 2013-10-27 at the Wayback Machine, CAP1 Archived 2013-11-02 at the Wayback Machine, HACD1 Archived 2013-10-07 at the Wayback Machine, LNPEP Archived 2012-09-13 at the Wayback Machine, SERPINB6 Archived 2013 ...