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For Developers

Define serverless bioinformatics workflows using plain Python & deploy associated no-code interfaces with single command.

For Biologists

Access our suite of pre-built, optimized workflows designed to address common bioinformatics challenges.

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Bring your own workflow

Latch providers a robust development toolkit that allows developers to upload an existing pipeline written in Snakemake, Nextflow, or Python. Key benefits of the Latch SDK:
  • Instant no-code interfaces for accessibility and publication.
  • Containerization and versioning of every registered change.
  • Reliable and scalable managed cloud infrastructure.
  • Automatically run workflows on top of folders in Latch Data.

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Get Started with the Latch SDK

Create a new workflow with our Python SDK

The fastest way to get started-ideal for those with ad-hoc scripts to create a workflow.

Upload a Nextflow pipeline

Create GUIs from Nextflow projects with minimal added boilerplate & code.

Upload a Snakemake pipeline

Integrate your existing Snakemake pipelines with Latch, and easily create a GUI.

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Out-of-the-box Verified Workflows

Latch offers ready-to-use Verified for a variety of common assays, including bulk RNA-seq, scRNA-seq, AlphaFold, ColabFold, and more. These Verified Workflows are developed using the Latch Python SDK by Latch engineers and have been used by top 10 pharmaceutical companies and hundreds of biotech firms to enhance their research and discovery efforts. Examples of Latch Verified Workflows:

Bulk RNA-seq

Perform alignment and quantification on Bulk RNA-Sequencing reads.

DESeq2 (Differential Expression)

Estimate variance-mean dependence in count data from high-throughput sequencing assays.

Pathway Enrichment Analysis

Use differential expression contrast data to calculate the gene ontology and pathways for the most significant genes.

AlphaFold

Generate highly accurate protein structures predictions.

ColabFold

The ColabFold version of AlphaFold2 is optimized for extremely fast predictions on small proteins.

CRISPResso2

Analysis of deep sequencing data for rapid and intuitive interpretation of genome editing experiments.