16S rRNA — Nuclyra
Loading Nuclyra…
Service · Bioinformatics Pipeline

16S rRNA

16S rRNA amplicon pipelines for microbial community profiling — from raw reads to taxonomy, diversity metrics and publication-ready figures.

Who this is for

TYPICAL CLIENT

A lab that needs fast, cost-effective community composition, not full functional profiling

Usually a microbiome researcher, clinical microbiologist or environmental scientist who needs a reliable read on bacterial community composition across many samples, without the cost or turnaround time of shotgun sequencing.

What you walk away with

Six concrete deliverables, not a slide deck.

This is exactly what transfers to you at the end of this 16S rRNA engagement.

Primer trimming & quality filtering

Reads trimmed to your primer set and quality-filtered before any taxonomic inference.

ASV inference

Amplicon sequence variants inferred with DADA2 or QIIME2, giving exact sequence resolution instead of clustered OTUs.

Taxonomic classification

ASVs classified against a curated 16S reference database down to the finest resolvable taxonomic level.

Alpha & beta diversity analysis

Within- and between-sample diversity metrics with ordination plots for group comparison.

Differential abundance testing

Statistical testing to identify taxa that differ significantly between your defined sample groups.

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

Primer-aware quality filtering

Reads trimmed and filtered against your specific 16S primer set and target hypervariable region.

ASV inference (DADA2/QIIME2)

Exact amplicon sequence variants inferred instead of coarser OTU clustering, for finer taxonomic resolution.

Taxonomic classification

Classification against curated 16S databases (SILVA, Greengenes2) down to genus or species level where resolvable.

Diversity & statistical analysis

Alpha/beta diversity and differential abundance testing delivered as figures your team can use directly.

In practice

What this looks like in a real engagement

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

Gut microbiome intervention study

Pre/post samples from a dietary or therapeutic intervention profiled for shifts in community composition.

Soil or environmental 16S survey

Environmental samples across sites or seasons profiled to characterize bacterial community differences.

Clinical dysbiosis screening

Patient samples screened for taxonomic markers associated with a defined clinical condition.

Why it matters

Why 16S is still the right first question for a lot of microbiome work.

Not every project needs shotgun-level functional resolution. When the question is “how does community composition differ between these groups,” 16S rRNA sequencing answers it quickly, at lower cost, and at a scale — hundreds of samples — that makes shotgun sequencing impractical.

We build 16S pipelines around ASV inference rather than older OTU clustering, so results are directly comparable across studies and reference databases without re-processing.

16S rRNA structure and sequence diagram from a bacterial cell showing the 30S and 50S ribosomal subunits
How we deliver it

How an engagement runs

Four stages, from sample intake to delivery.

Stage 01 — Trim

Primer trim & filter

Reads are trimmed to the primer set and quality-filtered before variant inference.

Stage 02 — Infer

ASV inference

Amplicon sequence variants are inferred and a feature table is built across all samples.

Stage 03 — Classify

Taxonomic classification

ASVs are classified against a curated reference database to the finest resolvable level.

Stage 04 — Analyze & handoff

Diversity analysis & hand off

Diversity statistics and comparison figures are generated, documented and delivered.

Tooling

What we build it with

DADA2QIIME2SILVAGreengenes2NextflowphyloseqMultiQCvegan
At species-comparison scale across hundreds of samples, 16S still gets you a reliable answer faster than shotgun ever will.
Questions we get

Before you reach out

V3–V4 is the most common choice for general bacterial profiling; we can advise based on your organism of interest and existing study comparability.

We use ASV inference by default (via DADA2) since it resolves exact sequence variants and stays comparable across studies, unlike similarity-clustered OTUs.

The pipeline is built for batch processing — we’ve run cohorts from a handful of samples up to several hundred in a single batch.

Let’s talk

Have a cohort waiting on a community composition answer?

Send us your sample count and study design — we’ll tell you honestly whether 16S gives you the resolution this study needs.