NGS Research

Our wide range of end-to-end next generation sequencing research services are performed on the latest Illumina platforms in our laboratory located in Silicon Valley, CA. We generate and analyze large variety of genomic and transcriptomic sequencing data to deliver biological insights that benefit your research program. We provide standard and customizable bioinformatic workflows and support our clients with our expertise to deeply interrogate data and identify relevant features to their studies.

Discover Your Service

Library preparation services using inputs from all NGS applications

Applications Offered
Illumina, Takara, Kapa & Others

  • Whole Genome, Exome & Targeted Sequencing
  • Epigenetic Sequencing
  • Metagenomic Sequencing
  • Transcriptome Sequencing
  • Single Cell Sequencing
  • TCR & BCR Sequencing

Sequencing Platforms
Illumina Solutions

  • NovaSeq
  • HiSeq X
  • HiSeq 4000
  • HiSeq 2500
  • MiSeq

Analysis & Visualization
MedGenome & Other Solutions

  • De Novo Assembly
  • Variant calling, annotation and interpretation
  • Gene expression, pathway analysis, gene fusion detection, splicing
  • Neoepitope prediction and prioritization
  • Tumor microenvironment analysis

Why Choose MedGenome

 

BioFX Bioinformatics Service

  • Streamlined pipeline for fast & scalable analysis
  • Customized reporting
  • Interactive reports
  • Publication-ready figures
  • Improve data interpretation with support from MedGenome's team of experts

 

Ordering and Data Delivery

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

 

MedGenome Customer Portal


Portal Walkthrough
Navigating & Exploring FAQ Section

Order Walkthrough
Sample Manifest Upload & Printing Shipping Documents

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