Precision whole genome sequencing – all within two weeks
Cost-effective whole genome sequencing on Illumina NovaSeqTM X Plus and Ultima UG 100TM
Illumina NovaSeqTM X Plus and Ultima UG 100TM
Highly accurate short read sequencing that produces data for clinical and research applications
High quality services in a CLIA-certified, CAP-accredited lab
Ensure data quality with QA oversight, all performed with CLIA-trained personnel in a CLIA-certified lab with CLIA-qualified equipment
Wet and dry lab expertise
Inocras accepts multiple sample types (somatic and germline) with optional DNA extraction, library prep, or sequencing-only services. We return data to you as flexible raw data files (FASTQ, BAM, CRAM, etc), curated data files (typically VCF) or an Inocras Dx product report.
Submit a request
Thank you for your interest in partnering with us to advance your genomic research. Please fill out and submit this form and we will get in touch with you within 48 hours to address your project needs. We look forward to working with you.
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