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mukesh13
2025-09-04 02:33:03 +05:30
parent 3f803ac0c9
commit 78a56a061b
65 changed files with 2234 additions and 992 deletions
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49
app/dna-sequencing/snp-genotyping/components/SNPIntroduction.jsx
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@ -3,7 +3,10 @@ import IntroductionLayout from '../../../components/shared/IntroductionLayout';
const SNPIntroduction = () => {
const contentItems = [
"SNP-based genotyping identifies single nucleotide polymorphisms (SNPs) across the genome, offering insights into genetic diversity, disease associations, and trait inheritance. It is widely applied in population genetics, evolutionary biology, and plant and animal breeding."
"ddRAD sequencing (Double Digest Restriction-site Associated DNA) is based on the Restriction Fragmentation technique combined with Next-Generation Sequencing (NGS). It is a robust approach for \"genotyping and SNP discovery\" that doesn't require a reference genome.",
"The ddRAD workflow utilizes the precise cut-site specificity of restriction endonucleases to create library fragments from unique genomic regions. These fragments are then selected and sequenced, capturing data from identical genomic regions across samples.",
"In the bioinformatics analysis, reads are aligned to either a reference genome or de novo assembly to detect SNVs and other genetic variations. This analysis supports studies on genetic diversity, population structure, and trait associations, with advanced tools enabling the processing of large datasets to achieve high genotyping accuracy.",
"With the potential to develop hundreds to tens of thousands of genetic markers, ddRAD is ideal for applications in population genetics, germplasm assessment, marker-trait associations, GWAS, and QTL mapping. Its targeted, reproducible approach makes it a valuable tool for ecological and agricultural genomics."
];
const advantageItems = [
"Allows for precise identification of genetic variations at a single nucleotide level, enabling detailed mapping of genetic diversity.",
@ -12,7 +15,6 @@ const SNPIntroduction = () => {
"Can reveal associations between genetic variations and complex traits, allowing researchers to identify genetic contributors to health, disease, or productivity in agriculture."
];
const serviceTypes = [
"DNA Sequencing",
"RNA Sequencing",
@ -20,19 +22,36 @@ const SNPIntroduction = () => {
];
return (
<IntroductionLayout
introTitle="Introduction and Workflow"
advantageTitle="Advantage"
introItems={contentItems}
advantageItems={advantageItems}
imageUrl="/images/dna/SNP-based_genotyping_(ddRAD).png"
imageAlt="SNP Genotyping Overview"
badgeText="ISO CERTIFIED"
serviceTypes={serviceTypes}
backgroundColor="#f8f9fa"
badgeColor="bg-teal-600"
useParagraphs={true}
/>
<>
{/* Main Heading Section */}
<section className="py-5 lg:py-5">
<div className="container-fluid px-4 lg:px-6">
<div className="lg:px-6">
<h1 className="text-3xl font-bold text-teal-700 mb-2">
Double Digest Restriction-site Associated DNA (ddRAD) Sequencing
</h1>
<p className="text-base leading-relaxed" style={{color: '#faae31'}}>
Focused, Cost-Effective Genotyping with ddRAD
</p>
</div>
</div>
</section>
{/* Introduction Layout */}
<IntroductionLayout
introTitle="Introduction and Workflow"
advantageTitle="Advantage"
introItems={contentItems}
advantageItems={advantageItems}
imageUrl="/images/dna/SNP-based_genotyping_(ddRAD).png"
imageAlt="SNP Genotyping Overview"
badgeText="ISO CERTIFIED"
serviceTypes={serviceTypes}
backgroundColor="#f8f9fa"
badgeColor="bg-teal-600"
useParagraphs={true}
/>
</>
);
};