
Supported access to Ultima sequencing through the applications lab.
Technology Access Program combines access to Ultima's sequencer fleet with application specialists and bioinformatics support. Researchers can obtain sequencing and tailored analysis through one service rather than operating the instrumentation themselves.
The program accommodates several sample and library inputs and supplies CRAM or FASTQ output for downstream tools. Consultation and continuing technical support accompany the sequencing workflow, including assistance with interpretation and subsequent experiments.
Technology Access Program provides a project-based route to Ultima sequencing through the provider's own applications laboratory. The described service starts with research requirements and sample preparation before technicians conduct sequencing and quality-control checks.
The resulting data and analysis are delivered online, and the laboratory continues to support interpretation and integration into research workflows. Ultima also maintains a Certified Service Provider network as a separate route to sequencing services.
Prospective Technology Access Program customers discuss sequencing needs with an Ultima Genomics sales specialist through the provider's inquiry form. The specialist's stated remit includes pricing questions, application support, and potential sequencing projects.
The program begins with consultation on project objectives and application-specific data requirements. That inquiry process connects the requested sequencing work with specialist guidance before the customer submits samples to the in-house laboratory.
Technology Access Program lets researchers commission sequencing projects using Ultima Genomics' in-house applications laboratory and sequencer fleet. Its workflow includes consultation, sample submission, sequencing, quality control, analysis, delivery, and continuing technical support.
Supported inputs include extracted DNA and RNA, native Ultima libraries, and existing libraries. The program covers whole-genome and single-cell sequencing, proteomics, and rare-event detection applications, with results delivered in formats such as CRAM and FASTQ.