Genomics

Running genomics workflows at scale shouldn’t require managing cloud infrastructure or writing complex scripts. Yet for many researchers, turning raw sequencing data into actionable results can be a time-consuming, technical challenge.

Camber simplifies this process by providing a cloud-based environment with built-in support for tools and pipelines commonly used in genomics. With Camber, you can run workflows using Nextflow—a popular and reproducible workflow language—directly from the command line or through the web interface.

Upload your data, choose or customize a workflow, and execute powerful genomic analyses in minutes—not days. Whether you’re doing variant calling, methylation profiling, or RNA-seq, Camber helps you spend more time on the science and less on setup.

Browse the examples below to see how easy it is to get started with your own genomic workflows:

Variant Calling

Detects genetic variants from whole genome or targeted sequencing data across any species with a reference genome

[nextflow cpu]

Metagenomic Profiling

Process short and long sequencing reads for metagenomic analysis, including QC, taxonomy, assembly, and annotation

[nextflow cpu]

Methylation Sequencing

Processes bisulfite sequencing data for DNA methylation analysis, performing read alignment, QC, and reporting

[nextflow cpu]

RNA Sequencing

Process RNA sequencing data to perform QC, alignment, and quantification, producing a gene expression matrix

[nextflow cpu]