36 lines
2.0 KiB
JavaScript
36 lines
2.0 KiB
JavaScript
// ResequencingIntroduction.jsx
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import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
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const ResequencingIntroduction = () => {
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const contentItems = [
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"Whole Genome Resequencing involves sequencing an organism's entire genome where reference genome is already available. Unlike de novo sequencing, which builds a genome from scratch, resequencing focuses on identifying variations and differences compared to a previously known reference genome.",
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"The workflow involves DNA isolation, fragmentation, and sequencing to generate millions of short reads.",
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"These reads undergo alignment to a reference genome, followed by the analysis of genetic variations using advanced bioinformatics tools.",
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"It enables detailed analysis of genetic variations across diverse species like humans, plants, and bacteria."
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];
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const advantageItems = [
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"Provides a detailed examination of an organism's entire genome, revealing all genetic variations compared to a reference genome.",
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"Enables accurate identification of single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants, crucial for understanding genetic diversity and disease mechanisms.",
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"Facilitates the discovery of genetic markers associated with diseases, guiding personalized treatment approaches.",
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"Supports diverse studies including evolutionary biology, agricultural genetics, and microbial genomics, enhancing insights into genetic adaptations and relationships across species."
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];
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return (
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<IntroductionLayout
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introTitle="Introduction and Workflow"
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advantageTitle="Advantage"
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introItems={contentItems}
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advantageItems={advantageItems}
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imageUrl="/images/dna/resequencing-workflow.png"
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imageAlt="Resequencing Workflow"
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badgeText="RESEQUENCING"
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badgeSubtext="Change only sequencing and analysis by adding it from whole exome"
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backgroundColor="#f8f9fa"
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badgeColor="bg-teal-600"
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useParagraphs={true}
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/>
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);
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};
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export default ResequencingIntroduction; |