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Fully customizable, end-to-end workflows executed by independent verified labs. Guided RFQ design, capability-matched routing and blind competing quotes — tailored to your samples and research goals.
Our services
Compare sample requirements, library chemistries, sequencing platforms and analysis deliverables across verified providers — submit one RFQ, receive competing quotes.
Sequence microbial, plant and animal genomes for assembly or resequencing.
Characterise microbial communities in mixed samples.
Measure gene expression or study transcript isoforms.
Profile DNA methylation with methods suited to your study.
Sequence individual DNA fragments for confirmation and identification.
Submit prepared libraries for sequencing on a compatible platform.
Request analysis with sequencing or use an existing dataset for a standalone project.
Validated platforms & instrument partners
The Gateway advantage
Run genomic, transcriptomic, epigenomic and proteomic assays under a single RFQ — no batch drift from fragmented vendors.
Your RFQ goes only to facilities whose platforms, sample types and service categories actually fit the work.
Credentials, equipment claims and track record checked against Syntax criteria before any provider can quote.
Validated workflows for FFPE blocks, long-term archived specimens and fresh material — including low-input down to picogram scale.
Our RFQ workflows
Every project follows a standardized, tracking-validated flow designed to preserve sample integrity and guarantee transparent delivery.
Step 1
Capture organism, sample count, requested output, analysis type, deadline and attachments in one guided form.
Step 2
The RFQ is routed to approved providers whose registered capabilities match your requirements.
Step 3
Providers submit pricing, taxes, turnaround, platforms and exclusions — invisible to each other.
Step 4
Compare side-by-side, select an offer, then track sample handoff through the status pipeline.
Step 5
Results land in your private project channel; raw genomic data stays at the lab or moves via secure links.
Bioinformatics
Every service can pair with one of three analysis packages — specify the tier in your RFQ and providers quote accordingly.
Best for teams running their own downstream analysis.
Best for teams that want results interpreted for them.
Best for novel, custom, or multi-omic study designs.
Included with every tier
FASTQ files
Sequencer QC report
Alignment files (BAM)
Processed results tables
Publication-ready figures
Secure delivery — SFTP, AWS or Google Cloud
Resources & programs
FAQs
Answers on RFQs, blind quoting, samples, turnaround and data handling. Still unsure? Talk to our team.
Share your samples and goals — a doctoral-level scientist responds within one business day with a study plan and competing blind quotes.
Administered by Syntax of Life Private Limited
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