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// EpigenomicsAdvantages.jsx
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import AdvantagesLayout from '../../../components/shared/AdvantagesLayout';
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const EpigenomicsAdvantages = () => {
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const advantageItems = [
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"Provides comprehensive analysis of epigenetic modifications including DNA methylation, histone modifications, and chromatin accessibility, offering insights into gene regulation mechanisms.",
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"Enables single-base resolution mapping of epigenetic marks across the genome, allowing for precise identification of regulatory elements and their modifications.",
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"Reveals epigenetic alterations associated with diseases, development, and environmental responses, providing insights into cellular memory and inheritance patterns.",
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"Identifies potential therapeutic targets and biomarkers for epigenetic-based treatments, supporting the development of personalized medicine approaches."
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];
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return (
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<AdvantagesLayout
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title="Advantages of Epigenomics Sequencing"
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advantageItems={advantageItems}
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/>
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);
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};
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export default EpigenomicsAdvantages;
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// EpigenomicsIntroduction.jsx
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import IntroductionLayout from '../../../components/shared/IntroductionLayout';
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const EpigenomicsIntroduction = () => {
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const contentItems = [
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"Epigenomics Sequencing is a comprehensive approach to analyze epigenetic modifications across genomes, providing enriched genomic view of cellular memory and gene regulation.",
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"The workflow includes isolating DNA, fragmenting it, capturing the regions of interest followed by sequencing to produce millions of short reads.",
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"In the bioinformatics analysis, these reads are aligned to a known reference genome to detect genomic alterations and epigenetic modifications.",
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"It is a powerful tool for diverse genomic studies, capable of sequencing humans, livestock, plants, bacteria, and disease-related microbes."
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];
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const serviceTypes = [
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"Whole Genome Bisulphite Sequencing (WGBS)",
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"Chip Sequencing",
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"ATAC Sequencing"
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];
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return (
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<IntroductionLayout
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title="Introduction and Workflow"
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contentItems={contentItems}
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imageUrl="/images/epigenomics-overview.png"
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imageAlt="Epigenomics Overview"
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badgeText="EPIGENOMICS"
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serviceTypes={serviceTypes}
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backgroundColor="#f8f9fa"
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badgeColor="bg-teal-600"
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useParagraphs={true}
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/>
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);
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};
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export default EpigenomicsIntroduction;
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// EpigenomicsSpecifications.jsx
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import Link from 'next/link';
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import SpecificationsLayout from '../../../components/shared/SpecificationsLayout';
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const EpigenomicsSpecifications = () => {
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const specificationItems = [
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{
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icon: "/images/homepage-2/NGS-Icons-45.svg",
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title: "Sample Requirement",
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renderContent: () => (
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<div>
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<div className="mb-4">
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<p className="text-gray-600">Genomic DNA, Cultivated cells, Blood, tissues, and other samples.</p>
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</div>
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<div className="mt-4 text-sm">
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<strong>
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Please refer to{' '}
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<Link href="/sample-submission-guideline" className="text-teal-600 underline hover:text-teal-700">
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sample submission guidelines
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</Link>
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{' '}or{' '}
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<Link href="/contact-us" className="text-teal-600 underline hover:text-teal-700">
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Contact Us!
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</Link>
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</strong>
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</div>
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</div>
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)
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},
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{
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icon: "/images/homepage-1/service/Advantages-NGS-Icons-20.svg",
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title: "Sequencing Platform",
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content: "Illumina NovaSeq 6000/ NovaSeq X"
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},
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{
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icon: "/images/service/social-support.png",
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title: "Deliverables",
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renderContent: () => (
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<ul className="list-disc pl-5 space-y-2 text-gray-600 text-start">
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<li>The original sequencing data</li>
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<li>Experimental results</li>
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<li>Bioinformatics and Data Analysis Report</li>
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<li>Details in Epigenomics Sequencing (customizable)</li>
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</ul>
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)
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}
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];
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return (
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<SpecificationsLayout
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title="Service Specifications"
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specificationItems={specificationItems}
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/>
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);
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};
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export default EpigenomicsSpecifications;
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