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  2. Functional genomics - Wikipedia

    en.wikipedia.org/wiki/Functional_genomics

    Functional genomics uses mostly multiplex techniques to measure the abundance of many or all gene products such as mRNAs or proteins within a biological sample. A more focused functional genomics approach might test the function of all variants of one gene and quantify the effects of mutants by using sequencing as a readout of activity.

  3. Genetics nursing - Wikipedia

    en.wikipedia.org/wiki/Genetics_nursing

    Also, competent nursing practice now requires the incorporation of genetic and genomic knowledge and skills in order to: Recognize when one's own attitudes and values related to genetic and genomic science may affect care provided to clients. Advocate for clients access to desired genetic/genomic services and/or resources including support groups.

  4. List of biological databases - Wikipedia

    en.wikipedia.org/wiki/List_of_biological_databases

    ConsensusPathDB: a molecular functional interaction database, integrating information from 12 others; Entrez (National Center for Biotechnology Information) Neuroscience Information Framework (University of California, San Diego): integrates hundreds of neuroscience relevant resources; many are listed below

  5. Omics - Wikipedia

    en.wikipedia.org/wiki/Omics

    The suffix -ome as used in molecular biology refers to a totality of some sort; it is an example of a "neo-suffix" formed by abstraction from various Greek terms in -ωμα, a sequence that does not form an identifiable suffix in Greek. Functional genomics aims at identifying the functions of as many genes as possible of a given organism. It ...

  6. Clinical metagenomic sequencing - Wikipedia

    en.wikipedia.org/wiki/Clinical_metagenomic...

    One type of sequencing method can be used in preference to another depending on the type of the sample, for a genomic sample assembly-based methods is used; for a metagenomic sample it is preferable to use read-based methods. [10] Metagenomic sequencing methods have provided better results than genomics, due to these present fewer false negatives.

  7. SNV calling from NGS data - Wikipedia

    en.wikipedia.org/wiki/SNV_calling_from_NGS_data

    The calculation of prior probabilities depends on available data from the genome being studied, and the type of analysis being performed. For studies where good reference data containing frequencies of known mutations is available (for example, in studying human genome data), these known frequencies of genotypes in the population can be used to estimate priors.

  8. Convergent Functional Genomics - Wikipedia

    en.wikipedia.org/wiki/Convergent_Functional_Genomics

    Convergent Functional Genomics (CFG) Developed by Alexander Niculescu, MD, PhD, and collaborators starting in 1999, [1] it is an approach for identifying and ...

  9. Functional cloning - Wikipedia

    en.wikipedia.org/wiki/Functional_cloning

    Functional cloning is a molecular cloning technique that relies on prior knowledge of the encoded protein’s sequence or function for gene identification. [ 1 ] [ 2 ] [ 3 ] In this assay, a genomic or cDNA library is screened to identify the genetic sequence of a protein of interest.