From sample to result.

Human whole-genome sequencing at 30x coverage, 100 Gb nominal output; delivers raw sequencing reads (FASTQ), with bioinformatics available as a separate service.

Mouse whole-genome sequencing at 30x mean coverage; delivers BAM/CRAM and VCF.

Human whole-genome sequencing at 30x coverage, 120 Gb robust output with additional depth margin; delivers raw sequencing reads (FASTQ), with bioinformatics available as a separate service.

Low-pass human whole-genome sequencing at 5x coverage; delivers raw sequencing reads (FASTQ), cost-efficient for GWAS-scale work.

Human whole-genome sequencing at 50x mean coverage for improved rare-variant sensitivity.

Human whole-genome sequencing at 100x deep coverage for tumour-normal and low-allele-fraction analysis.

WGS library preparation only, delivering sequencing-ready libraries without sequencing.

Whole-exome sequencing at 60x mean on-target coverage for research use.

Whole-exome sequencing at 60x mean on-target coverage with diagnostic-grade coverage guarantees.

Whole-exome sequencing at 120x mean on-target coverage for high-sensitivity and somatic applications.

Targeted methylome sequencing via hybrid capture at 250x coverage, covering around 3.9 million CpG sites.

Total RNA sequencing with ribosomal RNA depletion at around 50 million paired-end reads; captures coding and non-coding RNA.

mRNA sequencing with polyA selection at around 15 million paired-end reads; cost-efficient expression screening.

mRNA sequencing with polyA selection at around 30 million paired-end reads; standard depth for differential expression.

Small RNA sequencing for microRNA, snoRNA and piRNA profiling.

Genome-wide DNA methylation profiling across more than 935,000 CpG sites; bisulfite conversion included.

EPIC v2 genome-wide methylation profiling with a prioritised 10-working-day turnaround.

Targeted methylation screening across a curated set of roughly 285,000 clinically relevant CpG sites.

Standalone bisulfite conversion of genomic DNA for downstream methylation workflows.

Sequence alignment plus copy-number variant detection; delivers BAM/CRAM and CNV calls.

Sequence alignment plus SNV and indel calling; delivers BAM/CRAM and an annotated VCF.

Combined variant and copy-number analysis; delivers an annotated VCF together with CNV calls.

Microbiome data analysis for 16S amplicon data; delivers taxonomy and diversity metrics.

RNA-seq alignment with expression quantification; delivers FPKM/TPM tables.

RNA-seq alignment with expression quantification and RNA variant calling.

DNA extraction bundled with a downstream analysis service; includes RNase digestion.

Standalone DNA extraction delivering genomic DNA with a QC report.

Gel purification of PCR products with quality control of size and concentration.

RNA extraction with discounted bulk pricing; includes DNase digestion and RIN QC.

Standard RNA extraction with DNase digestion and RIN quality control.

DNA extraction from buccal swab samples; typical yield 0.5-5 ug.

DNA extraction from 200 ul buffy coat; typical yield 3-10 ug.

DNA extraction from 600 ul buffy coat for higher yield.

DNA extraction from small-volume saliva samples (under 600 ul).

DNA extraction from 200 ul EDTA whole blood; typical yield 5-10 ug.

DNA extraction from 2 ml EDTA whole blood; typical yield 30-80 ug.

DNA extraction from 5 ml EDTA whole blood for high yield.

DNA extraction from 7 ml EDTA whole blood; high yield for demanding workflows.

DNA extraction from 10 ml EDTA whole blood; maximum yield for biobanking.

RNA extraction service with RIN quality control included.

DNA extraction from 4 ml saliva; higher yield suitable for sequencing input.

DNA extraction from stool samples; standard input for microbiome sequencing.

DNA extraction from 400 ul EDTA whole blood.

DNA extraction from a dried blood spot (DBS).

DNA sequencing library preparation from 100-200 ng input, ready for Illumina sequencing.

Stranded mRNA sequencing library preparation with polyA selection.

Total RNA sequencing library preparation with ribosomal RNA depletion.

Tagmentation-based sequencing library preparation from as little as 1 ng input.

Hybrid-capture library preparation for targeted panels with UMI-based error correction.

Directional bacterial RNA library preparation with bacterial rRNA depletion.

Whole-transcriptome gene-level expression profiling; available for human, mouse and rat.

Whole-transcriptome gene-level expression profiling with a low-input protocol for FFPE or sub-nanogram samples.

Exon-level expression profiling covering coding and long non-coding transcripts; human, mouse and rat.

Exon-level expression profiling with a low-input protocol for FFPE or limited-material samples.

High-resolution human transcript- and exon-level expression profiling with extensive splice-variant coverage.

Human Transcriptome Array 2.0 profiling with a low-input protocol for limited clinical material.

Classic gene-level expression profiling of around 47,000 transcripts; comparable to historical GEO datasets.

Gene-level expression profiling with exon coverage for human, mouse or rat (Gene 1.0/2.0 ST).

Gene-level human expression profiling in a 96-well format with express turnaround.

Profiling of mature microRNAs and other small RNAs across all miRBase species.

High-throughput whole-transcript expression profiling in a 96-well plate format.

Classic rat whole-genome expression profiling with around 31,000 probe sets.

Exon-level gene expression profiling for mouse and rat with cross-species comparability.

Exon-level plant gene expression profiling for rice and Arabidopsis.

Classic Arabidopsis genome expression profiling covering around 22,500 genes.

Genome-wide SNP genotyping on the Global Screening Array with multi-disease and pharmacogenomic content.

Global Screening Array genotyping with added psychiatric risk-marker content.

Genome-wide genotyping on the Global Diversity Array with broad ethnic representation and pharmacogenomic content.

Genome-wide SNP genotyping on the Infinium Global Screening Array (GSA-24+MD).

High-throughput Axiom SNP genotyping in a 384-well plate format; content depends on the chosen panel.

Axiom SNP genotyping in a 96-well plate format; content depends on the chosen panel.

Axiom SNP genotyping in a 96-well mini format for smaller sample batches.

Multiplex-PCR genotyping for targeted SNP panels; cost-efficient for defined marker sets.

Illumina Infinium SNP genotyping with external quality control for regulated workflows.

Illumina Infinium SNP genotyping for research workflows.

High-resolution molecular karyotyping with around 750,000 markers; detects CNVs, ROH and mosaicism.

High-density molecular karyotyping with around 2.67 million markers for clinical-grade resolution.

CytoScan 750K molecular karyotyping as a full service including DNA isolation from blood or buffy coat.

CytoScan HD molecular karyotyping as a full service including DNA isolation from blood or buffy coat.

Low-resolution molecular karyotyping on an Illumina 700K microarray; delivers the GenomeStudio project and raw idat data.

Low-resolution molecular karyotyping with a basic report: karyogram chromosome plot, cnvPartition analysis (500 kb cut-off) and molecular sex determination.

Low-resolution molecular karyotyping with a full report: basic report plus hot-spot CNV analysis.

16S rRNA V3-V4 amplicon sequencing for microbial community profiling at genus to species level.

16S rRNA V4 amplicon sequencing for microbial community profiling with high throughput.

Shotgun metagenomic sequencing delivering taxonomic and functional community profiles.

Standard quantitative PCR, priced per reaction; delivers Cq values, optionally absolute quantification.

SARS-CoV-2 detection by RT-qPCR; delivers a qualitative result with Cq values.

TaqMan SNP genotyping using IDT assays, priced per sample.

TaqMan SNP genotyping using Thermo Fisher assays, priced per sample.