24 lines
1.2 KiB
JavaScript
24 lines
1.2 KiB
JavaScript
// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeIntroduction.jsx
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import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
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const ExomeIntroduction = () => {
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const contentItems = [
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"Whole Exome Sequencing (WES) is sequencing of only protein-coding regions (<2% of the genome, also known as exome), which accounts for 80-85% of disease-related variants.",
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"The workflow involves DNA isolation, fragmentation, capturing exonic regions, and sequencing to generate millions of short reads. In the bioinformatics analysis, these reads undergo alignment to a reference genome, followed by the variant calling (SNVs, Indels) and data analysis.",
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"Pinpoints potential disease-causing mutations, providing valuable insights for population genetics, genetic disease research, and cancer studies.",
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"Extensively utilized in diagnostic setting to detect clinically relevant genomic alterations associated with phenotype of the patient."
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];
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return (
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<IntroductionLayout
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title="Introduction and Workflow"
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contentItems={contentItems}
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imageUrl="/images/dna.jpg"
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imageAlt="DNA Structure"
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useParagraphs={true}
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/>
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);
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};
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export default ExomeIntroduction; |