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Sequencing and analysis, matched to your research question.
Every service is a complete project, from design review to figures, backed by the 100% Complete Project Guarantee.
One quote. No add-ons.
Free design review
Method, depth and platform checked before you spend.
Kit and courier paid
Sample kit, courier and customs paperwork, organised by us.
QC before library prep
Multi-level QC, with the result before we spend your money.
Sample rescue
Recovery pipelines for low-input, degraded and FFPE material.
Custom library prep
Protocol and platform chosen for your question.
Custom analysis
Built around your hypothesis by our own team.
Figures and Methods
Publication-quality figures and a written Methods section.
Reviewer re-analysis
Included whenever reviewers ask for something different.
Complications at €0
The 100% Complete Project Guarantee, in every quote.
Eight services, one way of working.
16S, ITS & 18S amplicon sequencing
Find out which bacteria, fungi or other organisms live in your samples and how communities differ between groups. Reads one marker gene, so many samples fit the budget.
Shotgun metagenomics
Sequence all the DNA in a sample to name microbes down to species, see which gene functions they carry and rebuild genomes. Spike-ins turn percentages into cell counts.
RNA sequencing
Measure how active every gene is, compare your groups and see which biological pathways the changed genes belong to.
Whole-genome & exome sequencing
Read a whole genome or all protein-coding genes, find the variants and get a short, classified list of the ones that could matter.
De novo genome assembly
Build a genome for an organism that has none, from long reads, with checks for completeness, contamination and species identity.
DNA methylation
Measure DNA methylation at single CpG sites and find the regions and promoters that gained or lost methylation between your groups.
ddRAD & SNP genotyping
Read the same small part of the genome in every individual to find SNP markers, then analyse population structure, diversity and relatedness, or design a SNP array.
Bioinformatics only
Already have sequencing data? We check it, analyse it around your question and deliver figures, tables and a Methods section.
Platform-neutral. We choose the instrument for your question.
We often price the same project on two platforms side by side, so you choose with the numbers in front of you.
| Platform | Instruments we run projects on | Configurations we use | Best for |
|---|---|---|---|
| Illumina | NovaSeq X Plus · NovaSeq 6000 · NextSeq 2000 · NextSeq 1000 · MiSeq | PE150 on 25B lanes · XLEAP-SBS chemistry · P1 600-cycle 2×300 bp | Amplicon, shotgun, RNA-seq, genomes, exomes, methylation, genotyping |
| Oxford Nanopore | PromethION · GridION · MinION | Whole flow cells (~60 Gb) or multiplexed at 18 Gb+ | Long-read and hybrid genome assembly, methylation from native DNA |
| PacBio | Revio · Sequel II / IIe | HiFi reads on SMRT Cells | Accurate, contiguous genome assemblies, species identification, methylation from native DNA |
Not sure which service fits?
Describe the question and the samples. We recommend a method, including when a cheaper one is enough.
- info@ngsalytics.com Projects, samples and invoices
What to put in your first email
- What your samples are, and how many you have
- The question you want the data to answer
- Your deadline: a paper, a grant or a reviewer
- Anything unusual: low input, FFPE, low biomass