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// EpigenomicsAdvantages.jsx
import AdvantagesLayout from '../../../components/shared/AdvantagesLayout';
const EpigenomicsAdvantages = () => {
const advantageItems = [
"Provides comprehensive analysis of epigenetic modifications including DNA methylation, histone modifications, and chromatin accessibility, offering insights into gene regulation mechanisms.",
"Enables single-base resolution mapping of epigenetic marks across the genome, allowing for precise identification of regulatory elements and their modifications.",
"Reveals epigenetic alterations associated with diseases, development, and environmental responses, providing insights into cellular memory and inheritance patterns.",
"Identifies potential therapeutic targets and biomarkers for epigenetic-based treatments, supporting the development of personalized medicine approaches."
];
return (
<AdvantagesLayout
title="Advantages of Epigenomics Sequencing"
advantageItems={advantageItems}
/>
);
};
export default EpigenomicsAdvantages;

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// EpigenomicsIntroduction.jsx
import IntroductionLayout from '../../../components/shared/IntroductionLayout';
const EpigenomicsIntroduction = () => {
const contentItems = [
"Epigenomics Sequencing is a comprehensive approach to analyze epigenetic modifications across genomes, providing enriched genomic view of cellular memory and gene regulation.",
"The workflow includes isolating DNA, fragmenting it, capturing the regions of interest followed by sequencing to produce millions of short reads.",
"In the bioinformatics analysis, these reads are aligned to a known reference genome to detect genomic alterations and epigenetic modifications.",
"It is a powerful tool for diverse genomic studies, capable of sequencing humans, livestock, plants, bacteria, and disease-related microbes."
];
const serviceTypes = [
"Whole Genome Bisulphite Sequencing (WGBS)",
"Chip Sequencing",
"ATAC Sequencing"
];
return (
<IntroductionLayout
title="Introduction and Workflow"
contentItems={contentItems}
imageUrl="/images/epigenomics-overview.png"
imageAlt="Epigenomics Overview"
badgeText="EPIGENOMICS"
serviceTypes={serviceTypes}
backgroundColor="#f8f9fa"
badgeColor="bg-teal-600"
useParagraphs={true}
/>
);
};
export default EpigenomicsIntroduction;

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// EpigenomicsSpecifications.jsx
import Link from 'next/link';
import SpecificationsLayout from '../../../components/shared/SpecificationsLayout';
const EpigenomicsSpecifications = () => {
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 Epigenomics Sequencing (customizable)</li>
</ul>
)
}
];
return (
<SpecificationsLayout
title="Service Specifications"
specificationItems={specificationItems}
/>
);
};
export default EpigenomicsSpecifications;