DNA SEQUENCING

Every nucleotide counts

high-quality sequencing for unlocking insights

High coverage, cost efficient and fast turnaround times

Whole Genome and Exome Sequencing applications are widely used in a number of applications including diagnostics to identify clinically actionable mutations, neo-antigen predictions and genome wide association studies for complex diseases.

We have experience executing whole genome and whole exome projects at population scale. We have mapped unique variants in South Asian genomes which are under-represented in public reference databases and are valuable for discovery research.

We have experience processing diverse samples including cells, blood, tissues and FFPE.

Download the technical sheets

Whole Genome/ Whole Exome Workflow

Whole Genome/ Whole Exome Workflow

WHOLE GENOME/WHOLE EXOME SEQUENCING SERVICES

Our key features include

WES/WGS key features

Support with experimental design and selection of appropriate workflow dependent on analysis needs.

WES/WGS key features

Experienced in processing a wide range of sample types with options for low input and degraded samples.

WES/WGS key features

End-to-end solutions for extraction, sample QC, library preparation, sequencing and bioinformatics analysis.

WES/WGS key features

Advanced analysis offering includes custom visuals and publication ready figures for improved data interpretation.

Service highlights

Our pipelines are built using state-of-the-art analysis tools for germline, somatic, structural variant and copy number analysis and annotation. We offer standard and custom workflows to support variant calling across different species.

Service highlights
  • Detailed data quality, alignment and coverage stats.
Service highlights
  • Distribution of base changes for SNVs.
Service highlights
  • Circos plots for SNPs, Indels, CNVs and SV representation for selected genes.
Service highlights
  • Lollipop plots showing variants for genes.
Service highlights
  • Explore mutation signatures.

Resources

White papers and technical resources

Resource Video
Video
WES/WGS Report Walkthrough
QC report
QC report
Whole-genome Sequencing/Whole-exome QC Report
Whitepaper
Whitepaper
Denovo Genome Assembly Solutions at MedGenome

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how to order

Starting a project with MedGenome

MedGenome's customer portal allows for easy sample submission and sample tracking during lab processing. Using our portal ensures data QC, raw data and interactive analysis reports are delivered securely.

Our process is simple

Request a quote Request a quote
We create your project file We create your project
Upload sample details Upload sample details
Submit documents and ship samples Submit documents and ship samples
We process and analyze your samples We process and analyze your samples
Your data is delivered to you Your data is delivered to you

News

Featured articles

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MedGenome appoints Martin Dewhurst as Chairman of Advisory Board
Conference

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MedGenome achieves 10x Genomics Certified Service provider qualification for single cell sequencing
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MedGenome to Exhibit Proprietary Sequencing and Informatics Solutions at the AACR 2023
Investment

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MedGenome ties-up with Emmes to bridge gaps in rare diseases
Research Grant

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MedGenome, in collaboration with PacBio, announces a de novo genome assembly and annotation grant
Vaccine

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Gallbladder cancer vaccine candidates identified

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