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Sanger Sequencing

High-accuracy Sanger (dideoxy) sequencing for plasmid verification, PCR-product confirmation, mutation screening and difficult templates — the gold standard for single-gene validation, delivered with fast turnaround and free re-runs on QC failures.

What we offer

Single- & double-pass reads up to ~1,000 bp

GC-rich, hairpin & difficult templates

96-well plate high-throughput processing

Free reaction QC and re-runs

What you receive

Raw FASTQ data with QC reports

Reference-aligned BAM / CRAM files

Annotated variant calls (VCF)

De novo / hybrid assembly contigs

Coverage & quality metrics dashboard

Publication-ready summary report

Workflow

Sample & QC

Extraction, QC and library prep under documented, standardised protocols.

Sequencing / Processing

Calibrated runs and pipelines on validated platforms.

Bioinformatics

HPC-backed assembly, alignment, variant calling and annotation.

Report & Insight

Publication-ready reports, with a dedicated project manager throughout.

Frequently asked

We accept tissue, whole blood, cell pellets, extracted DNA/RNA and a range of environmental and microbial samples. Our team advises on collection and shipping for each project.

Specifications

MethodSanger (dideoxy)

Read lengthUp to ~1,000 bp

FormatSingle tube · 96-well

Turnaround2 – 4 days

Get a tailored quote

Tell us your sample type, scope and timelines — we'll respond within one business day.

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