Docker config

app/dna-sequencing/whole-genome-sequencing/resequencing/components/ResequencingIntroduction.jsx

@@ -0,0 +1,28 @@
+// ResequencingIntroduction.jsx
+
+import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
+
+const ResequencingIntroduction = () => {
+  const contentItems = [
+    "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.",
+    "The workflow involves DNA isolation, fragmentation, and sequencing to generate millions of short reads.",
+    "These reads undergo alignment to a reference genome, followed by the analysis of genetic variations using advanced bioinformatics tools.",
+    "It enables detailed analysis of genetic variations across diverse species like humans, plants, and bacteria."
+  ];
+
+  return (
+    <IntroductionLayout
+      title="Introduction and Workflow"
+      contentItems={contentItems}
+      imageUrl="/images/resequencing-workflow.png"
+      imageAlt="Resequencing Workflow"
+      badgeText="RESEQUENCING"
+      badgeSubtext="Change only sequencing and analysis by adding it from whole exome"
+      backgroundColor="#f8f9fa"
+      badgeColor="bg-teal-600"
+      useParagraphs={true}
+    />
+  );
+};
+
+export default ResequencingIntroduction;