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Whole Genome Sequencing

Comprehensive sequencing of an entire genome — capturing coding and non-coding regions, structural variants and SNPs at base-pair resolution. Delivered on Illumina short-read, PacBio HiFi and Oxford Nanopore long-read platforms, with hybrid assembly for the most complete, contiguous genomes.

What we offer

Short, long & hybrid read strategies

De novo & reference-based assembly

SNP, indel & structural-variant calling

30x–100x+ configurable coverage

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

PlatformsIllumina · PacBio · ONT

Read strategyShort / Long / Hybrid

Coverage30x – 100x+

Sample inputTissue · Blood · Cells

Turnaround3 – 6 weeks

Get a tailored quote

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

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