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// app/dna-sequencing/whole-genome-sequencing/components/WGSAdvantages.jsx
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import AdvantagesLayout from '../../../components/shared/AdvantagesLayout';
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const WGSAdvantages = () => {
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const advantageItems = [
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"Provides a comprehensive, high-resolution view of the genome, surpassing the coverage offered by targeted sequencing.",
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"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.",
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"Generates large volumes of data quickly, facilitating the assembly of novel genomes.",
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"Uncovers genomic diversity, taxonomic classifications, and evolutionary relationships, enhancing our understanding of biological complexity."
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];
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return (
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<AdvantagesLayout
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title="Advantages of Whole Genome 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 WGSAdvantages;
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// app/dna-sequencing/whole-genome-sequencing/components/WGSIntroduction.jsx
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import IntroductionLayout from '../../../components/shared/IntroductionLayout';
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const WGSIntroduction = () => {
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const contentItems = [
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"Whole Genome Sequencing (WGS) is a comprehensive approach to analyze entire genomes base-by-base, providing a complete genomic view.",
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"The workflow includes isolating DNA, fragmenting it, and sequencing to produce millions of short reads.",
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"In the bioinformatics analysis, these reads are then assembled to construct the genome or aligned to a known reference genome.",
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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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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/denovo-workflow.png"
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imageAlt="Sample Process Steps"
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useParagraphs={true}
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/>
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);
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};
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export default WGSIntroduction;
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// app/dna-sequencing/whole-genome-sequencing/components/WGSSpecifications.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 WGSSpecifications = () => {
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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
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href="/sample-submission-guideline"
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className="text-teal-600 underline hover:text-teal-700"
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>
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sample submission guidelines
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</Link>
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{' '}or{' '}
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<Link
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href="/contact-us"
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className="text-teal-600 underline hover:text-teal-700"
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>
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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 Whole Genome Denovo 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 WGSSpecifications;
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