Skip to main content
Workflow templates are pre-built analysis pipelines curated by the Biomni Lab team. They help you get started quickly with common bioinformatics tasks.

Using a Template

From the Chat Input

Click the + Workflow button in the chat input area to browse available templates:
  1. Click + Workflow next to the chat input
  2. Browse templates by category or search
  3. Click a template to see its description and requirements
  4. Click Use Template to apply it
  5. Provide the required input files when prompted

From Suggested Templates

When you start a new task, relevant workflow templates appear in the chat area based on common use cases:
  1. Click on a template to see what it does
  2. Click Use Template to apply it
  3. Provide the required input files when prompted

Template Examples

RNA-seq Differential Expression

Performs full RNA-seq analysis from raw reads:
  1. Quality control with FastQC
  2. Alignment with STAR
  3. Quantification with featureCounts
  4. Differential expression with DESeq2
  5. Visualization with volcano plots and heatmaps
Required inputs: Paired-end FASTQ files, sample metadata

Single-cell Clustering

Analyzes single-cell RNA-seq data:
  1. Quality filtering
  2. Normalization and scaling
  3. Dimensionality reduction (PCA, UMAP)
  4. Clustering
  5. Marker gene identification
Required inputs: Count matrix or 10x Genomics output

Variant Calling

Identifies genetic variants from sequencing data:
  1. Alignment to reference genome
  2. Mark duplicates
  3. Base quality recalibration
  4. Call variants with GATK
  5. Variant annotation with VEP
Required inputs: FASTQ files, reference genome