Docker config
This commit is contained in:
mukesh13
@ -0,0 +1,20 @@
|
||||
// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeAdvantages.jsx
|
||||
import AdvantagesLayout from '../../../../components/shared/AdvantagesLayout';
|
||||
|
||||
const ExomeAdvantages = () => {
|
||||
const advantageItems = [
|
||||
"Cost-effective as compared to Whole Genome Sequencing (WGS), making it accessible to a broader range of researchers and clinicians.",
|
||||
"WES offers extensive sequencing of exonic regions, improving the detection of single-nucleotide variants (SNVs), copy number variants (CNVs), and insertions/deletions (InDels) with a sensitivity comparable to WGS, ensuring high accuracy in identifying genetic variants.",
|
||||
"WES generates a smaller data set compared to WGS, facilitating faster and easier data analysis, which can expedite research and diagnostic processes.",
|
||||
"WES is widely used in both medical and agricultural fields, supporting advancements in disease diagnosis, personalized medicine, and crop improvement. Provides a comprehensive, high-resolution view of the genome, surpassing the coverage offered by targeted sequencing."
|
||||
];
|
||||
|
||||
return (
|
||||
<AdvantagesLayout
|
||||
title="Advantages of Whole Exome Sequencing"
|
||||
advantageItems={advantageItems}
|
||||
/>
|
||||
);
|
||||
};
|
||||
|
||||
export default ExomeAdvantages;
|
||||
@ -0,0 +1,22 @@
|
||||
// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeApplications.jsx
|
||||
import ApplicationsLayout from '../../../../components/shared/ApplicationsLayout';
|
||||
|
||||
const ExomeApplications = () => {
|
||||
const applicationItems = [
|
||||
"Genetic Disorder Diagnosis- Identifies genetic mutations associated with rare and inherited disorders by focusing on the exonic regions where most disease-related variants occur. This enables accurate diagnosis and personalized treatment plans.",
|
||||
"Cancer Research- Detects somatic mutations in cancer genomes, providing insights into tumor biology, identifying potential biomarkers for early detection, and guiding targeted therapies for more effective treatment.",
|
||||
"Drug Development- Assists in the discovery of new drug targets and the development of precision medicine by revealing the genetic underpinnings of diseases and how genetic variations affect drug responses.",
|
||||
"Population Genetics- Explores genetic variations in diverse populations to understand genetic diversity, evolutionary processes, and the genetic basis of complex traits and diseases, aiding in public health and epidemiological studies.",
|
||||
"Functional Genomics- Provides insights into gene function and regulation by identifying coding mutations that impact protein function, contributing to our understanding of gene-disease relationships and mechanisms of gene action.",
|
||||
"Plant Genomics- Supports crop improvement and plant breeding programs by revealing the genetic basis of desirable traits and enhancing the understanding of plant genomes."
|
||||
];
|
||||
|
||||
return (
|
||||
<ApplicationsLayout
|
||||
title="Applications of Whole Exome Sequencing"
|
||||
applicationItems={applicationItems}
|
||||
/>
|
||||
);
|
||||
};
|
||||
|
||||
export default ExomeApplications;
|
||||
@ -0,0 +1,24 @@
|
||||
// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeIntroduction.jsx
|
||||
|
||||
import IntroductionLayout from '../../../../components/shared/IntroductionLayout';
|
||||
|
||||
const ExomeIntroduction = () => {
|
||||
const contentItems = [
|
||||
"Whole Exome Sequencing (WES) is sequencing of only protein-coding regions (<2% of the genome, also known as exome), which accounts for 80-85% of disease-related variants.",
|
||||
"The workflow involves DNA isolation, fragmentation, capturing exonic regions, and sequencing to generate millions of short reads. In the bioinformatics analysis, these reads undergo alignment to a reference genome, followed by the variant calling (SNVs, Indels) and data analysis.",
|
||||
"Pinpoints potential disease-causing mutations, providing valuable insights for population genetics, genetic disease research, and cancer studies.",
|
||||
"Extensively utilized in diagnostic setting to detect clinically relevant genomic alterations associated with phenotype of the patient."
|
||||
];
|
||||
|
||||
return (
|
||||
<IntroductionLayout
|
||||
title="Introduction and Workflow"
|
||||
contentItems={contentItems}
|
||||
imageUrl="/images/dna.jpg"
|
||||
imageAlt="DNA Structure"
|
||||
useParagraphs={true}
|
||||
/>
|
||||
);
|
||||
};
|
||||
|
||||
export default ExomeIntroduction;
|
||||
@ -0,0 +1,63 @@
|
||||
// app/dna-sequencing/enrichment-sequencing/whole-exome/components/ExomeSpecifications.jsx
|
||||
import Link from 'next/link';
|
||||
import SpecificationsLayout from '../../../../components/shared/SpecificationsLayout';
|
||||
|
||||
const ExomeSpecifications = () => {
|
||||
const specificationItems = [
|
||||
{
|
||||
icon: "/images/homepage-2/NGS-Icons-45.svg",
|
||||
title: "Sample Requirement",
|
||||
renderContent: () => (
|
||||
<div>
|
||||
<div className="mb-3">
|
||||
<strong>• Genomic DNA</strong>
|
||||
</div>
|
||||
<div className="mb-3">
|
||||
<strong>• Cultivated cells, Blood, tissues, Fresh Frozen, FFPE</strong>
|
||||
<span className="block text-sm text-gray-500 mt-1">
|
||||
(formalin-fixed paraffin-embedded)
|
||||
</span>
|
||||
</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 Whole Exome Sequencing (customizable)</li>
|
||||
</ul>
|
||||
)
|
||||
}
|
||||
];
|
||||
|
||||
return (
|
||||
<SpecificationsLayout
|
||||
title="Service Specifications"
|
||||
specificationItems={specificationItems}
|
||||
/>
|
||||
);
|
||||
};
|
||||
|
||||
export default ExomeSpecifications;
|
||||
Reference in New Issue
Block a user