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// ResequencingAdvantages.jsx
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import AdvantagesLayout from '../../../../components/shared/AdvantagesLayout';
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const ResequencingAdvantages = () => {
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const advantageItems = [
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"Provides a detailed examination of an organism's entire genome, revealing all genetic variations compared to a reference genome.",
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"Enables accurate identification of single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants, crucial for understanding genetic diversity and disease mechanisms.",
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"Facilitates the discovery of genetic markers associated with diseases, guiding personalized treatment approaches.",
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"Supports diverse studies including evolutionary biology, agricultural genetics, and microbial genomics, enhancing insights into genetic adaptations and relationships across species."
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];
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return (
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<AdvantagesLayout
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title="Advantages of Whole Genome ReSequencing"
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advantageItems={advantageItems}
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/>
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);
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};
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export default ResequencingAdvantages;
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// ResequencingApplications.jsx
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import ApplicationsLayout from '../../../../components/shared/ApplicationsLayout';
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const ResequencingApplications = () => {
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const applicationItems = [
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"Genetic Variation Discovery- Identifies and characterizes genetic variations, including single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants, across different individuals or populations, aiding in the study of genetic diversity and evolution.",
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"Disease Research- Helps in pinpointing genetic mutations and variants associated with genetic disorders, complex diseases, and rare conditions, enhancing our understanding of disease mechanisms and enabling the development of targeted therapies.",
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"Personalized Medicine- Facilitates the tailoring of medical treatments based on an individual's genetic profile, allowing for more precise and effective interventions and drug responses.",
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"Population Genetics- Assists in studying the genetic makeup of populations to understand evolutionary processes, migration patterns, and adaptation to environmental changes, providing insights into the genetic basis of traits and diseases.",
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"Agricultural Genomics- Identifies genetic markers linked to desirable traits and maps quantitative trait loci (QTL) to enhance selective breeding and improve characteristics such as yield, disease resistance, and stress tolerance. It also supports genome-wide association studies (GWAS) to connect genetic variants with specific traits or diseases."
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];
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return (
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<ApplicationsLayout
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title="Applications of Whole Genome ReSequencing"
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applicationItems={applicationItems}
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/>
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);
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};
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export default ResequencingApplications;
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// ResequencingIntroduction.jsx
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import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
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const ResequencingIntroduction = () => {
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const contentItems = [
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"Whole Genome Resequencing involves sequencing an organism's entire genome where reference genome is already available. Unlike de novo sequencing, which builds a genome from scratch, resequencing focuses on identifying variations and differences compared to a previously known reference genome.",
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"The workflow involves DNA isolation, fragmentation, and sequencing to generate millions of short reads.",
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"These reads undergo alignment to a reference genome, followed by the analysis of genetic variations using advanced bioinformatics tools.",
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"It enables detailed analysis of genetic variations across diverse species like humans, plants, and bacteria."
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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/resequencing-workflow.png"
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imageAlt="Resequencing Workflow"
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badgeText="RESEQUENCING"
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badgeSubtext="Change only sequencing and analysis by adding it from whole exome"
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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 ResequencingIntroduction;
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// ResequencingSpecifications.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 ResequencingSpecifications = () => {
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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 of Whole Genome ReSequencing (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 ResequencingSpecifications;
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import TitleBar from '../../../components/shared/TitleBar';
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import ResequencingIntroduction from './components/ResequencingIntroduction';
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import ResequencingAdvantages from './components/ResequencingAdvantages';
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import ResequencingApplications from './components/ResequencingApplications';
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import ResequencingSpecifications from './components/ResequencingSpecifications';
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import PageLayout from '../../../components/Layout/PageLayout';
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export default function WholeGenomeResequencingPage() {
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const breadcrumbs = [
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{ label: 'Home', href: '/' },
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{ label: 'Research', href: '/research' },
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{ label: 'Whole Genome Sequencing', href: '/dna-sequencing/whole-genome-sequencing' },
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{ label: 'Whole Genome ReSequencing', current: true }
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];
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return (
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<PageLayout fixedHeader={true}>
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<TitleBar
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title="Whole Genome ReSequencing"
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desc="Unraveling Genomic Complexity with Re-Sequencing"
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breadcrumbs={breadcrumbs}
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/>
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<div className="page-content">
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<ResequencingIntroduction />
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<ResequencingAdvantages />
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<ResequencingApplications />
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<ResequencingSpecifications />
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</div>
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</PageLayout>
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);
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}
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