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
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.

Request a Quote