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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Machines are complex structures consisting of movable, pin-connected multi-force members that work together to transmit forces. One example of a machine is the cutting plier, which is used to cut wires by applying forces to its handles. When equal and opposite forces are exerted on the handles of the cutting plier, they cause the cutting edges to come together and apply equal and opposite reaction forces on the wire, which are greater than the applied forces.
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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
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Severe Dengue Prognosis Using Human Genome Data and Machine Learning.

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    Machine learning predicts dengue severity using only human genome data. This approach identifies individuals at high risk for severe dengue, improving disease management.

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    Area of Science:

    • Genetics
    • Immunology
    • Computational Biology

    Background:

    • Dengue is a major global arthropod-borne disease.
    • Current diagnostic methods for dengue phenotypes are often inaccurate.

    Purpose of the Study:

    • To develop a machine learning model for predicting dengue fever severity using only human genome data.
    • To identify genetic markers associated with dengue severity.

    Main Methods:

    • Genotyping of 102 Brazilian dengue patients and controls for 322 innate immunity single nucleotide polymorphisms (SNPs).
    • Utilizing a support vector machine (SVM) for feature selection and an artificial neural network (ANN) for classification.
    • Training the ANN on 13 key immune SNPs selected under dominant or recessive models.

    Main Results:

    • The ANN model achieved median accuracy greater than 86%.
    • The model demonstrated high sensitivity (over 98%) and specificity (over 51%) in classifying dengue fever versus severe dengue.
    • Identified 13 key immune SNPs crucial for accurate classification.

    Conclusions:

    • Human genome data alone can accurately predict dengue fever severity.
    • This genetic-based classification method can identify individuals at high risk for severe dengue, even before infection.
    • Genetic factors play a significant role in defining dengue phenotypes and can be leveraged for disease prediction and management.