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  2. High-throughput screening - Wikipedia

    en.wikipedia.org/wiki/High-throughput_screening

    High-throughput screening (HTS) is a method for scientific discovery especially used in drug discovery and relevant to the fields of biology, materials science [1] and chemistry. [ 2 ] [ 3 ] Using robotics , data processing/control software, liquid handling devices, and sensitive detectors, high-throughput screening allows a researcher to ...

  3. Phenotypic screening - Wikipedia

    en.wikipedia.org/wiki/Phenotypic_screening

    High-content screening where changes in the expression of several proteins can be simultaneously monitored is also often used. [9] [10] High-content imaging of dye-labeled cellular components can also reveal effects of compounds on cell cultures in vitro, distinguishing the phenotypic effects of a broad variety of drugs. [11]

  4. Phenotype microarray - Wikipedia

    en.wikipedia.org/wiki/Phenotype_microarray

    High-throughput phenotypic testing is increasingly important for exploring the biology of bacteria, fungi, yeasts, and animal cell lines such as human cancer cells.Just as DNA microarrays and proteomic technologies have made it possible to assay the expression level of thousands of genes or proteins all a once, phenotype microarrays (PMs) make it possible to quantitatively measure thousands of ...

  5. High throughput biology - Wikipedia

    en.wikipedia.org/wiki/High_throughput_biology

    Classical High throughput screening robotics are now being tied closer to cell biology, principally using technologies such as High-content screening.High throughput cell biology dictates methods that can take routine cell biology from low scale research to the speed and scale necessary to investigate complex systems, achieve high sample size, or efficiently screen through a collection.

  6. Chemoproteomics - Wikipedia

    en.wikipedia.org/wiki/Chemoproteomics

    The choice of a chemical library is less stringent than other high-throughput screening strategies owing to the lack of functional readouts, which would otherwise require deconvolution of the source compound that generates biological activity. Thus, the typical range for AS-MS is 400-3,000 compounds per pool. [20]

  7. Perturb-seq - Wikipedia

    en.wikipedia.org/wiki/Perturb-seq

    Perturb-seq can therefore combine the high throughput of forward genetics, in terms of the number of genetic perturbations, with the rich phenotype dimension of reverse genetics. [ 7 ] However, while a large and comprehensive amount of data can be a benefit, it can also present a major challenge.

  8. Hit selection - Wikipedia

    en.wikipedia.org/wiki/Hit_selection

    In high-throughput screening (HTS), one of the major goals is to select compounds (including small molecules, siRNAs, shRNA, genes, et al.) with a desired size of inhibition or activation effects. A compound with a desired size of effects in an HTS screen is called a hit.

  9. Marker-assisted selection - Wikipedia

    en.wikipedia.org/wiki/Marker-assisted_selection

    Marker assisted selection or marker aided selection (MAS) is an indirect selection process where a trait of interest is selected based on a marker (morphological, biochemical or DNA/RNA variation) linked to a trait of interest (e.g. productivity, disease resistance, abiotic stress tolerance, and quality), rather than on the trait itself.

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