// app/dna-sequencing/whole-genome-sequencing/components/WGSIntroduction.jsx

import IntroductionLayout from '../../../components/shared/IntroductionLayout';

const WGSIntroduction = () => {
  const contentItems = [
    "Whole Genome Sequencing (WGS) is a comprehensive approach to analyze entire genomes base-by-base, providing a complete genomic view.",
    "The workflow includes isolating DNA, fragmenting it, and sequencing to produce millions of short reads.",
    "In the bioinformatics analysis, these reads are then assembled to construct the genome or aligned to a known reference genome.",
    "It is a powerful tool for diverse genomic studies, capable of sequencing humans, livestock, plants, bacteria, and disease-related microbes."
  ];
  const advantageItems = [
    "Provides a comprehensive, high-resolution view of the genome, surpassing the coverage offered by targeted sequencing.",
    "Identifies both small (SNVs, CNVs, InDels) and large structural variants that may be missed with targeted approaches, offering valuable insights into inherited genetic conditions and characterizing mutations driving cancer progression.",
    "Generates large volumes of data quickly, facilitating the assembly of novel genomes.",
    "Uncovers genomic diversity, taxonomic classifications, and evolutionary relationships, enhancing our understanding of biological complexity."
  ];

  return (
    <IntroductionLayout
      introTitle="Introduction and Workflow"
      advantageTitle="Advantage"
      introItems={contentItems}
      advantageItems={advantageItems}
      imageUrl="/images/dna/whole_genome_seq-normal_denovo.png"
      imageAlt="Sample Process Steps"
      useParagraphs={true}
    />
  );
};

export default WGSIntroduction;