Docker config

app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeIntroduction.jsx

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+// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeIntroduction.jsx
+
+import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
+
+const ExomeIntroduction = () => {
+  const contentItems = [
+    "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.",
+    "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.",
+    "Pinpoints potential disease-causing mutations, providing valuable insights for population genetics, genetic disease research, and cancer studies.",
+    "Extensively utilized in diagnostic setting to detect clinically relevant genomic alterations associated with phenotype of the patient."
+  ];
+
+  return (
+    <IntroductionLayout
+      title="Introduction and Workflow"
+      contentItems={contentItems}
+      imageUrl="/images/dna.jpg"
+      imageAlt="DNA Structure"
+      useParagraphs={true}
+    />
+  );
+};
+
+export default ExomeIntroduction;