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mukesh13
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// app/dna-sequencing/hybrid-genome-sequencing/components/HybridAdvantages.jsx
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import AdvantagesLayout from '../../../components/shared/AdvantagesLayout';
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const HybridAdvantages = () => {
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const advantageItems = [
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"Combines long-read and short-read sequencing for more complete and accurate genome assemblies, effectively resolving complex regions and reducing gaps.",
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"Balances the cost efficiency of short-read sequencing with the detailed resolution of long-read sequencing, making it a budget-friendly choice for comprehensive genome analysis.",
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"Enhances detection of structural variants, such as large insertions and deletions, improving the understanding of genetic diversity and disease mechanisms.",
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"Provides better coverage of challenging genomic features, like high GC content and repetitive sequences, by leveraging the strengths of both sequencing technologies."
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];
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return (
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<AdvantagesLayout
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title="Advantages of Hybrid 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 HybridAdvantages;
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// app/dna-sequencing/hybrid-genome-sequencing/components/HybridApplications.jsx
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import ApplicationsLayout from '../../../components/shared/ApplicationsLayout';
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const HybridApplications = () => {
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const applicationItems = [
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"Comprehensive Genome Mapping- Hybrid genome sequencing is used to create detailed genome maps by combining the strengths of both short-read and long-read technologies, leading to more complete and accurate assemblies of complex genomes.",
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"Structural Variant Detection- This approach is effective in identifying structural variants, such as large deletions, duplications, and insertions, which are often challenging to detect with short-read sequencing alone.",
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"Genetic Diversity and Evolutionary Studies- It facilitates the study of genetic diversity and evolutionary processes by providing high-resolution data on genomic variations across different species and populations."
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];
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return (
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<ApplicationsLayout
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title="Applications of Hybrid Genome Sequencing"
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applicationItems={applicationItems}
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/>
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);
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};
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export default HybridApplications;
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// app/dna-sequencing/hybrid-genome-sequencing/components/HybridBioinformatics.jsx
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const HybridBioinformatics = () => {
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return (
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<section className="py-8 lg:py-12 bg-gray-50">
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<div className="container mx-auto max-w-none px-4 lg:px-6">
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<h2 className="text-gray-600 text-left pb-6 text-2xl lg:text-3xl font-normal mb-8">
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Bioinformatics Pipeline
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</h2>
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{/* Pipeline Image */}
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<div className="bg-white rounded-xl shadow-lg p-6 lg:p-8">
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<div className="flex justify-center">
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<img
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src="/images/bioinformatics-pipeline.jpg"
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alt="Bioinformatics Pipeline Workflow"
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className="max-w-full h-auto rounded-lg"
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/>
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</div>
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</div>
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</div>
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</section>
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);
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};
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export default HybridBioinformatics;
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// app/dna-sequencing/hybrid-genome-sequencing/components/HybridIntroduction.jsx
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import IntroductionLayout from '../../../components/shared/IntroductionLayout';
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const HybridIntroduction = () => {
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const contentItems = [
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"Hybrid sequencing integrates the accuracy of short-read sequencing (Illumina) with the comprehensive coverage of long-read sequencing (PacBio or Nanopore), ensuring detailed and complete genome assemblies.",
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"This approach involves sequencing the same sample with both technologies, which means different libraries are prepared for both the technology followed by sequencing.",
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"Following sequencing, advanced bioinformatics tools are used to align and integrate the long and short reads, enhancing variant detection and improving the resolution of complex genomic regions.",
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"Hybrid sequencing is applicable to a wide range of research areas, from complex genome assemblies to resolving repetitive regions and improving the quality of reference genomes."
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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/sample-process-steps.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 HybridIntroduction;
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// app/dna-sequencing/hybrid-genome-sequencing/components/HybridSpecifications.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 HybridSpecifications = () => {
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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">Blood, Tissue, 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 and PacBio/Oxford Nanopore"
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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 of Hybrid Genome 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 HybridSpecifications;
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64
app/dna-sequencing/hybrid-genome-sequencing/page.js
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64
app/dna-sequencing/hybrid-genome-sequencing/page.js
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// app/dna-sequencing/snp-genotyping/page.js
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import TitleBar from '../../components/shared/TitleBar';
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import HybridIntroduction from './components/HybridIntroduction';
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import HybridAdvantages from './components/HybridAdvantages';
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import HybridBioinformatics from './components/HybridBioinformatics';
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import HybridApplications from './components/HybridApplications';
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import HybridSpecifications from './components/HybridSpecifications';
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import PageLayout from '../../components/Layout/PageLayout';
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export const metadata = {
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title: 'Hybrid Genome Sequencing - Operify Tech',
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description: 'Unifying Technologies for Deeper Genomic Clarity - Comprehensive Genomics Through Combined Power',
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robots: 'noindex, follow',
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};
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export default function HybridGenomeSequencingPage() {
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const breadcrumbs = [
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{
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label: 'Home',
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href: '/',
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current: false
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},
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{
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label: 'Research',
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href: '/dna-sequencing',
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current: false
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},
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{
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label: 'Hybrid Genome Sequencing',
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href: null,
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current: true
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}
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];
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return (
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<PageLayout fixedHeader={true}>
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{/* Title Bar */}
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<TitleBar
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title="Hybrid Genome Sequencing"
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desc="Unifying Technologies for Deeper Genomic Clarity"
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breadcrumbs={breadcrumbs}
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backgroundImage="/images/bredcrumb.jpg"
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/>
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{/* Page Content */}
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<div className="page-content">
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{/* Introduction Section */}
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<HybridIntroduction />
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{/* Advantages Section */}
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<HybridAdvantages />
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{/* Bioinformatics Pipeline Section */}
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<HybridBioinformatics />
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{/* Applications Section */}
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<HybridApplications />
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{/* Specifications Section */}
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<HybridSpecifications />
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</div>
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</PageLayout>
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);
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}
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