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app/rna-sequencing/degradome-sequencing/components/DegradomeIntroduction.jsx

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+// app/rna-sequencing/degradome-sequencing/components/DegradomeIntroduction.jsx
+import IntroductionLayout from '../../../components/shared/IntroductionLayout';
+
+const DegradomeIntroduction = () => {
+  const contentItems = [
+    "Degradome sequencing, also called Parallel Analysis of RNA Ends (PARE), is a high-throughput technique to analyze RNA degradation products, uncovering RNA stability, miRNA targets, and regulatory networks.",
+    "Degradome Sequencing Workflow combines next-generation sequencing (NGS) with a modified 5' RACE method, involving RNA extraction, adapter ligation to capture degradation products, cDNA synthesis, and high-throughput sequencing to map RNA cleavage sites.",
+    "Bioinformatics analysis for Degradome Sequencing include data preprocessing, aligning reads to reference genomes, identifying miRNA/ta-siRNA cleavage sites, and quantifying cleaved targets, revealing RNA decay dynamics and regulatory mechanisms.",
+    "The method facilitates the discovery of novel miRNAs and ta-siRNAs, studies on miRNA-mediated gene regulation, and comparative RNA decay analysis across species, contributing to a comprehensive understanding of RNA life cycles."
+  ];
+
+  return (
+    <IntroductionLayout
+      title="Introduction and Workflow"
+      contentItems={contentItems}
+      badgeSubtext="Brochure from Degradome sequencing"
+      useParagraphs={true}
+    />
+  );
+};
+
+export default DegradomeIntroduction;