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// app/dna-sequencing/whole-genome-sequencing/components/WGSAdvantages.jsx
import AdvantagesLayout from '../../../components/shared/AdvantagesLayout';
const WGSAdvantages = () => {
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 (
<AdvantagesLayout
title="Advantages of Whole Genome Sequencing"
advantageItems={advantageItems}
/>
);
};
export default WGSAdvantages;

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// 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."
];
return (
<IntroductionLayout
title="Introduction and Workflow"
contentItems={contentItems}
imageUrl="/images/denovo-workflow.png"
imageAlt="Sample Process Steps"
useParagraphs={true}
/>
);
};
export default WGSIntroduction;

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// app/dna-sequencing/whole-genome-sequencing/components/WGSSpecifications.jsx
import Link from 'next/link';
import SpecificationsLayout from '../../../components/shared/SpecificationsLayout';
const WGSSpecifications = () => {
const specificationItems = [
{
icon: "/images/homepage-2/NGS-Icons-45.svg",
title: "Sample Requirement",
renderContent: () => (
<div>
<div className="mb-4">
<p className="text-gray-600">Genomic DNA, Cultivated cells, Blood, tissues, and other samples.</p>
</div>
<div className="mt-4 text-sm">
<strong>
PLEASE refer to{' '}
<Link
href="/sample-submission-guideline"
className="text-teal-600 underline hover:text-teal-700"
>
sample submission guidelines
</Link>
{' '}or{' '}
<Link
href="/contact-us"
className="text-teal-600 underline hover:text-teal-700"
>
Contact Us!
</Link>
</strong>
</div>
</div>
)
},
{
icon: "/images/homepage-1/service/Advantages-NGS-Icons-20.svg",
title: "Sequencing Platform",
content: "Illumina NovaSeq 6000/ NovaSeq X"
},
{
icon: "/images/service/social-support.png",
title: "Deliverables",
renderContent: () => (
<ul className="list-disc pl-5 space-y-2 text-gray-600 text-start">
<li>The original sequencing data</li>
<li>Experimental results</li>
<li>Bioinformatics and Data Analysis Report</li>
<li>Details in Whole Genome Denovo Sequencing (customizable)</li>
</ul>
)
}
];
return (
<SpecificationsLayout
title="Service Specifications"
specificationItems={specificationItems}
/>
);
};
export default WGSSpecifications;