Docker config

app/dna-sequencing/hybrid-genome-sequencing/components/HybridIntroduction.jsx

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+// app/dna-sequencing/hybrid-genome-sequencing/components/HybridIntroduction.jsx
+import IntroductionLayout from '../../../components/shared/IntroductionLayout';
+
+const HybridIntroduction = () => {
+  const contentItems = [
+    "Hybrid sequencing integrates the accuracy of short-read sequencing (Illumina) with the comprehensive coverage of long-read sequencing (PacBio or Nanopore), ensuring detailed and complete genome assemblies.",
+    "This approach involves sequencing the same sample with both technologies, which means different libraries are prepared for both the technology followed by sequencing.",
+    "Following sequencing, advanced bioinformatics tools are used to align and integrate the long and short reads, enhancing variant detection and improving the resolution of complex genomic regions.",
+    "Hybrid sequencing is applicable to a wide range of research areas, from complex genome assemblies to resolving repetitive regions and improving the quality of reference genomes."
+  ];
+
+  return (
+    <IntroductionLayout
+      title="Introduction and Workflow"
+      contentItems={contentItems}
+      imageUrl="/images/sample-process-steps.png"
+      imageAlt="Sample Process Steps"
+      useParagraphs={true}
+    />
+  );
+};
+
+export default HybridIntroduction;