Shotgun Metagenomics — Nuclyra
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Service · Bioinformatics Pipeline

Shotgun Metagenomics

Shotgun metagenomic pipelines that resolve taxonomic composition and functional potential straight from raw community DNA — no primer bias, no cultivation required.

Who this is for

TYPICAL CLIENT

A microbiome researcher who needs function, not just who’s there

Usually a microbiome researcher, environmental genomics lab or applied microbiology team who needs both taxonomic composition and functional gene content from a complex community sample — something a 16S-only approach can’t deliver.

What you walk away with

Six concrete deliverables, not a slide deck.

This is exactly what transfers to you at the end of this Shotgun Metagenomics engagement.

QC & host-read removal

Raw reads quality-filtered and screened against a host genome (e.g. human) to remove contaminating reads before analysis.

Taxonomic profiling report

Community composition resolved to species level using k-mer and marker-gene based classification.

Functional annotation

Gene and pathway abundance profiling to characterize the community’s functional, not just taxonomic, potential.

MAG assembly & binning

Metagenome-assembled genomes recovered and binned where samples support de novo assembly.

Diversity & abundance reports

Alpha and beta diversity metrics with per-sample and per-group comparison figures.

Full documentation & handoff session

Written documentation plus a recorded walkthrough so your team can operate the pipeline independently.

What's included

What this service includes

Taxonomic profiling

Species-level community composition using Kraken2/MetaPhlAn-based classification against curated reference databases.

Functional profiling

Gene family and pathway abundance estimated with HUMAnN-based functional annotation.

Assembly & MAG binning

De novo metagenome assembly with genome binning and quality assessment for recovered MAGs.

Diversity & statistical analysis

Alpha/beta diversity and group-wise statistical comparison delivered as publication-ready figures.

In practice

What this looks like in a real engagement

Three concrete examples of the kind of work this service covers.

Gut microbiome cohort study

Stool metagenomes from a clinical cohort profiled for taxonomic shifts and functional pathway differences between groups.

Environmental / soil metagenome survey

Soil or water community samples profiled to characterize microbial diversity across an environmental gradient.

Antimicrobial resistance gene screening

A community sample screened against curated AMR gene databases to quantify resistance gene abundance.

Why it matters

Why shotgun sequencing answers questions 16S profiling can’t.

16S rRNA sequencing tells you who is likely present, at genus level, with primer bias baked in. Shotgun metagenomics sequences all the DNA in a sample, so you get species and strain-level resolution and — critically — the functional gene content that actually explains what the community is doing.

We build shotgun pipelines that pair taxonomic and functional profiling by default, with optional assembly when a sample has enough depth to recover meaningful metagenome-assembled genomes.

Shotgun metagenomics workflow from soil and water sampling through sequencing to taxonomic and functional profiling
How we deliver it

How an engagement runs

Four stages, from sample intake to delivery.

Stage 01 — QC

QC & host removal

Reads are quality-filtered and screened to remove host or contaminant sequences.

Stage 02 — Profile

Taxonomic & functional profiling

Community composition and gene/pathway abundance are profiled in parallel.

Stage 03 — Assemble

Assembly & binning

Where depth supports it, reads are assembled and binned into draft metagenome-assembled genomes.

Stage 04 — Analyze & handoff

Diversity analysis & hand off

Diversity statistics and figures are generated, documented and delivered.

Tooling

What we build it with

Kraken2MetaPhlAnHUMAnNMEGAHITMetaBAT2NextflowCheckMQIIME2
Knowing which species are present tells you a story; knowing what genes they carry tells you what the community is actually doing.
Questions we get

Before you reach out

Shotgun sequencing profiles all DNA in a sample for species/strain-level and functional resolution; 16S targets one marker gene for genus-level composition at lower cost.

Typically 5–10 million reads per sample for taxonomic and functional profiling; deeper sequencing (20M+) is recommended if MAG assembly is a goal.

Yes — AMR gene screening against curated databases is available as part of the functional annotation step.

Let’s talk

Have community samples waiting on a functional answer?

Send us your sample type and research question — we’ll tell you honestly whether shotgun or 16S is the right sequencing strategy.