Bioinformatics Through
Natural Conversation

Transform complex genomics data into biological insights without writing a single line of code. Pipette understands your research goals and executes comprehensive analyses automatically.

70+
Bioinformatics tools
100%
No-Code Interface
24h
Early Access
Free
During Beta

Research-Grade Analysis Without Programming

Professional bioinformatics tools with the simplicity of natural language

Quality Control & Preprocessing

Automatic adapter trimming, quality filtering, and contamination screening with comprehensive QC reports.

"Check quality of my RNA-seq samples and remove adapters"

Statistical Analysis

DESeq2, edgeR, and limma pipelines with automatic batch effect correction and multiple testing adjustment.

"Find genes differentially expressed between treatment and control"

Visualization Suite

Publication-quality heatmaps, volcano plots, PCA, t-SNE, and UMAP with customizable parameters.

"Create a heatmap of top 50 variable genes"

Pathway & Network Analysis

GSEA, GO enrichment, KEGG pathway mapping, and protein interaction networks with STRING.

"What biological pathways are enriched in upregulated genes?"

Multi-Omics Integration

Combine RNA-seq, ChIP-seq, ATAC-seq, and proteomics data with MOFA or mixOmics.

"Integrate my RNA-seq with ATAC-seq peaks"

Reproducible Reports

Auto-generated methods sections with software versions and parameters. Export as notebooks.

"Generate methods section for my analysis"

Comprehensive Analysis Pipelines

Trusted workflows with validated tools and publication-ready outputs

RNA-seq Analysis

Differential expression, transcript quantification, splicing analysis, and fusion detection.

Tools: STAR, Salmon, DESeq2, rMATS
"Compare treated vs. control samples"

Single-Cell RNA-seq

Cell clustering, annotation, trajectory inference, and RNA velocity analysis.

Tools: Seurat, Scanpy, scVelo
"Identify cell populations and trajectories"

ChIP/ATAC-seq

Peak calling, motif discovery, chromatin accessibility, and differential binding.

Tools: MACS2, DiffBind, HOMER
"Find regulatory regions in disease tissue"

Variant Calling

SNP/Indel discovery, variant annotation, and functional prediction.

Tools: GATK, VEP, SnpEff
"Call variants and predict effects"

GWAS Analysis

Association testing, population stratification, and polygenic risk scores.

Tools: PLINK, GCTA, FINEMAP, rMVP
"Identify loci linked to phenotype"

Alternative Splicing

Detect differential splicing events, isoform switching, and splice junction analysis.

Tools: rMATS, STAR, Salmon
"Find splicing changes between conditions"

Frequently Asked Questions

Everything you need to know about using Pipette.bio

What is Pipette.bio?

Pipette.bio is a conversational AI agent for bioinformatics. It comes pre-loaded with open-source tools for NGS, genomics, and transcriptomics. You can analyze data and generate reproducible results without coding.

Where is my data stored?

Your files are uploaded to your private S3 bucket and processed in a secured environment. All data remains confidential and isolated.

How is reproducibility ensured?

Every analysis records its full data lineage: inputs, parameters, software versions, and outputs. You can download complete scripts to reproduce results.

Do I need to install anything?

No. Pipette runs entirely in your browser. Just log in, upload your data, and start your analysis through natural conversation.