16S / ITS amplicon
ASV-resolved profiling of bacterial, archaeal, or fungal communities from marker-gene surveys—higher resolution than legacy OTUs.
From raw reads to a clear picture of a microbial community. We run 16S/ITS amplicon and shotgun metagenomics pipelines—profiling who is there and what they can do, assembling genomes, and testing what shifts between groups—and hand back tables and figures documented for publication and review.
Metagenomics turns sequencing reads from a microbial community into a picture of its membership and function—which taxa are present, in what proportions, what they can do, and how that shifts between conditions. The hard part is rarely running a single tool; it is removing host and contaminant reads correctly, choosing amplicon or shotgun methods matched to your samples, handling compositional data with the right statistics, and documenting every decision so the result survives peer review.
We build and run that workflow for you. Whether you have a 16S amplicon survey of a hundred samples or shotgun data you want assembled into genomes, we take it through QC, profiling, diversity, and differential-abundance analysis using established, peer-reviewed tools—never opaque in-house black boxes—and return results with the tool versions and parameters recorded for full reproducibility.
One service spanning microbiome analysis end to end—from amplicon surveys to assembled genomes, taxonomy to function.
ASV-resolved profiling of bacterial, archaeal, or fungal communities from marker-gene surveys—higher resolution than legacy OTUs.
Species- and strain-level community composition from whole-metagenome reads, with relative-abundance estimation.
Gene-family and pathway abundance from shotgun data to move beyond “who is there” to “what can they do.”
De novo assembly and genome binning to recover metagenome-assembled genomes, with completeness and contamination QC.
Alpha- and beta-diversity, ordination, and compositional-aware tests for taxa that shift between groups.
Antimicrobial-resistance and virulence-gene profiling from reads or assemblies against curated reference databases.
Strain tracking, SNV-level resolution within species, and comparative genomics across recovered genomes.
Community gene expression to capture which functions are active—not just present—and how activity changes.
A transparent, best-practice sequence—each step chosen for your data and question and documented in the final report. Nothing is a black box.
Steps are adapted to your design: 16S vs. shotgun, high- vs. low-biomass, profiling only vs. assembly and MAGs. We confirm the plan with you before any compute begins.
Read QC, adapter and quality trimming, and removal of host and contaminant reads before profiling.
Tools: FastQC · MultiQC · fastp · KneadData
For amplicon: primer removal and ASV inference. For shotgun: quality-filtered reads ready for classification.
Tools: DADA2 · cutadapt · QIIME2
Taxonomy assigned against a curated reference—genus-level for amplicon, species and strain for shotgun.
Tools: QIIME2 · Kraken2 · Bracken · MetaPhlAn
For shotgun studies, de novo assembly and genome binning recover MAGs, with completeness and contamination checks.
Tools: MEGAHIT · MetaBAT2 · CheckM · GTDB-Tk
Gene-family and pathway abundance, plus AMR and virulence screening where the study calls for it.
Tools: HUMAnN3 · eggNOG · CARD
Alpha- and beta-diversity, ordination, and compositional-aware tests for taxa and functions that shift between groups.
Tools: phyloseq · vegan · ANCOM-BC · MaAsLin2
Feature and taxonomy tables, publication-quality figures, a QC report, and reproducible methods with every tool version.
Tools: ggplot2 · MultiQC · versioned methods manifest
We select from the field's standard toolkit rather than forcing every dataset through one pipeline. A representative set of what we work with:
A profile is only as good as the reference behind it. We build on the community's authoritative, versioned databases.
There is no single best method—only the right one for your question, samples, and budget. A quick orientation; we will help you decide.
| Dimension | 16S / ITS amplicon | Shotgun metagenomics | Metatranscriptomics |
|---|---|---|---|
| Measures | Who is there (marker gene) | Who is there & what they can do | What the community is doing |
| Resolution | Genus, sometimes species | Species & strain level | Active genes & pathways |
| Functional info | Inferred only | Gene & pathway content | Expressed function |
| Relative cost | Lowest; robust to host DNA | Higher; more data & compute | Higher; RNA handling required |
| Best suited to | Large surveys, low-biomass samples | Function, strains, MAG recovery | Activity & regulation questions |
Not just a feature table dropped in a folder—every output you need to interpret, publish, and reproduce the work.
Every pipeline follows documented best practices—correct host and contaminant removal, negative-control checks for low-biomass samples, and compositional-aware statistics—so differences between groups are real, not artifacts of uneven depth or contamination. We report read losses and rarefaction transparently. Each run records its tool versions, parameters, and reference database builds.
The practical payoff: your methods section writes itself, a reviewer can re-run the analysis, and a result from today can be reproduced a year from now. We will also tell you honestly when a design or sample size won't support the conclusion you're after.
What researchers and project leads most often ask before starting a microbiome project.
Tell us your organism, data type, and question—we'll scope it honestly, including if a different design would serve you better.