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Plus, get free data analysis for projects with 12 or more samples!


50x Coverage (5 Gb)

from $220/Sample

Germline Variant Discovery
Disease Genotyping

100x Coverage (10 Gb)

from $260/Sample

Somatic Mutation Discovery
Tumor/Normal Sequencing

≥200x Coverage (20+ Gb)

from $340/Sample

Low Frequency Mutation Detection
Tumor Mutational Burden Analysis

Features and Benefits
  • Ph.D.-level support throughout project
  • Data quality exceeding Illumina® benchmarks
  • U.S.-based sequencing
  • Agilent SureSelect chemistry provides uniform exome coverage

"Excellent data quality, effective communication, flexibility, and regular updates. I wish every CRO had such a high level of customer service."

Principal Scientist    

Major Pharmaceutical Company   

Get Promo Code

For technical support questions, please contact our Next Generation Sequencing team

+1 (908) 222-0711 ext. 1 |  NGS@genewiz.com

*Terms & Conditions: 44% off list price for human exome sequencing (research use only) with Value package. Advertised starting price is based on library preparation and sequencing of 20 genomic DNA samples on one lane of the Illumina® HiSeq™ with 2x150 bp configuration (~5 Gb/sample) and Value package turnaround time (starting at ≤30 business days). Free Standard DNA Analysis package, which includes mapping and SNP/INDEL discovery, for projects with 12 or more samples. Promo is for U.S.-based sequencing only. Additional charges for nucleic acid extraction and/or data analysis will apply. Institutions with contract pricing are excluded. Valid for NGS quotes issued by December 31, 2019. Promotion is not retroactive and cannot be combined with any other offerings. Terms and conditions are subject to change at any time without notice. Other restrictions may apply.