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  2. DECIPHER (software) - Wikipedia

    en.wikipedia.org/wiki/DECIPHER_(software)

    Sequence databases: import, maintain, view, and export, and interact with a massive number of sequences. Homology finding: rapidly query sequences for homologous hits among a set of target sequences or genomes.

  3. Learning classifier system - Wikipedia

    en.wikipedia.org/wiki/Learning_classifier_system

    A step-wise schematic illustrating a generic Michigan-style learning classifier system learning cycle performing supervised learning. Keeping in mind that LCS is a paradigm for genetic-based machine learning rather than a specific method, the following outlines key elements of a generic, modern (i.e. post-XCS) LCS algorithm.

  4. Sequence analysis - Wikipedia

    en.wikipedia.org/wiki/Sequence_analysis

    Variants can be annotated with information about genomic features, functional consequences, regulatory elements, and population frequencies using tools like ANNOVAR or SnpEff, [23] or custom scripts and pipeline. The output from this step is an annotation file in bed or txt format. [14]

  5. Binning (metagenomics) - Wikipedia

    en.wikipedia.org/wiki/Binning_(Metagenomics)

    PCAHIER, [17] another binning algorithm developed by the Georgia Institute of Technology., employs n-mer oligonucleotide frequencies as the features and adopts a hierarchical classifier (PCAHIER) for binning short metagenomic fragments. The principal component analysis was used to reduce the high dimensionality of the feature space.

  6. Holland's schema theorem - Wikipedia

    en.wikipedia.org/wiki/Holland's_schema_theorem

    Holland's schema theorem, also called the fundamental theorem of genetic algorithms, [1] is an inequality that results from coarse-graining an equation for evolutionary dynamics. The Schema Theorem says that short, low-order schemata with above-average fitness increase exponentially in frequency in successive generations.

  7. DECIPHER - Wikipedia

    en.wikipedia.org/wiki/DECIPHER

    DECIPHER is a web-based resource and database of genomic variation data from analysis of patient DNA. [ 1 ] [ 2 ] [ 3 ] It documents submicroscopic chromosome abnormalities ( microdeletions and duplications ) and pathogenic sequence variants (single nucleotide variants - SNVs, Insertions, Deletions, InDels), from over 25000 patients and maps ...

  8. DNA annotation - Wikipedia

    en.wikipedia.org/wiki/DNA_annotation

    Genomic browsers can be divided into web-based genomic browsers and stand-alone genomic browsers. The former use information from databases and can be classified into multiple-species (integrate sequence and annotations of multiple organisms and promote cross-species comparative analysis) and species-specific (focus on one organism and the ...

  9. John Henry Holland - Wikipedia

    en.wikipedia.org/wiki/John_Henry_Holland

    John Henry Holland was born on February 2, 1929 in Fort Wayne, Indiana, the elder child of [3] son of Gustave A. Holland (b. July 24, 1896, Russian Poland) and Mildred P. Gfroerer (b.