Docker config

app/dna-sequencing/epigenomics-sequencing/components/EpigenomicsIntroduction.jsx

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+// EpigenomicsIntroduction.jsx
+
+import IntroductionLayout from '../../../components/shared/IntroductionLayout';
+
+const EpigenomicsIntroduction = () => {
+  const contentItems = [
+    "Epigenomics Sequencing is a comprehensive approach to analyze epigenetic modifications across genomes, providing enriched genomic view of cellular memory and gene regulation.",
+    "The workflow includes isolating DNA, fragmenting it, capturing the regions of interest followed by sequencing to produce millions of short reads.",
+    "In the bioinformatics analysis, these reads are aligned to a known reference genome to detect genomic alterations and epigenetic modifications.",
+    "It is a powerful tool for diverse genomic studies, capable of sequencing humans, livestock, plants, bacteria, and disease-related microbes."
+  ];
+
+  const serviceTypes = [
+    "Whole Genome Bisulphite Sequencing (WGBS)",
+    "Chip Sequencing",
+    "ATAC Sequencing"
+  ];
+
+  return (
+    <IntroductionLayout
+      title="Introduction and Workflow"
+      contentItems={contentItems}
+      imageUrl="/images/epigenomics-overview.png"
+      imageAlt="Epigenomics Overview"
+      badgeText="EPIGENOMICS"
+      serviceTypes={serviceTypes}
+      backgroundColor="#f8f9fa"
+      badgeColor="bg-teal-600"
+      useParagraphs={true}
+    />
+  );
+};
+
+export default EpigenomicsIntroduction;