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Biomni provides access to a curated collection of biomedical databases, analysis tools, and software packages. Browse the Resources panel in the sidebar to explore what’s available.

Databases

Curated biomedical databases for reference data and annotations:
DatabaseDescriptionUse Cases
UniProtProtein sequences and functional annotationsProtein lookup, sequence retrieval, functional annotation
NCBI GeneGene-centric information across speciesGene IDs, symbols, descriptions, orthologs
PDBProtein 3D structuresStructure retrieval, visualization, docking prep
KEGGPathway and genome informationPathway mapping, enrichment analysis
GOGene Ontology annotationsFunctional classification, enrichment analysis
EnsemblGenome browser and annotationGenome coordinates, transcript info, variants
dbSNPSingle nucleotide polymorphismsSNP lookup, variant annotation
ClinVarClinical variant interpretationsPathogenicity, clinical significance
RefSeqReference sequencesTranscript and protein sequences
GEOGene expression datasetsPublic expression data, sample metadata
Database queries are cached for faster subsequent lookups. Results are refreshed weekly to ensure up-to-date information.

Alignment Tools

Tools for mapping sequencing reads to reference genomes:
ToolBest ForSpeedMemory
STARRNA-seq alignment, splice-awareFastHigh (30GB+)
Bowtie2DNA-seq, ChIP-seqFastLow
BWA-MEMDNA-seq, whole genomeFastMedium
HISAT2RNA-seq, low memoryMediumLow
Minimap2Long reads (PacBio, ONT)Very fastLow

When to Use Which Aligner

  • RNA-seq: Use STAR for best splice junction detection, HISAT2 for lower memory
  • DNA-seq/WGS: Use BWA-MEM for accuracy, Bowtie2 for speed
  • ChIP-seq: Bowtie2 with default settings
  • Long reads: Minimap2 for PacBio or Oxford Nanopore

Variant Calling Tools

Tools for identifying genetic variants:
ToolVariant TypesUse Case
GATK HaplotypeCallerSNPs, indelsGermline variants, best practices pipeline
GATK Mutect2SNPs, indelsSomatic variants (tumor/normal)
BCFtoolsSNPs, indelsFast variant calling, manipulation
FreeBayesSNPs, indels, MNPsHaplotype-based calling
DeepVariantSNPs, indelsDeep learning-based, high accuracy

RNA-seq Analysis

Packages for gene expression analysis:
PackageLanguageBest For
DESeq2RDifferential expression, small sample sizes
edgeRRDifferential expression, larger datasets
limma-voomRMicroarray and RNA-seq
featureCountsCLIRead counting, fast
HTSeqPythonRead counting, flexible
SalmonCLITranscript quantification, fast
kallistoCLITranscript quantification, pseudoalignment

Single-Cell Analysis

Tools for single-cell RNA-seq:
ToolLanguageFeatures
SeuratRComprehensive scRNA-seq, integration
ScanpyPythonScalable analysis, visualization
Cell RangerCLI10x Genomics data processing
scVIPythonDeep learning, batch correction
Monocle3RTrajectory analysis, pseudotime

Structural Biology

Tools for protein structure analysis:
ToolDescriptionGPU
AlphaFoldProtein structure predictionYes
ColabFoldFast AlphaFold with MSA serverYes
PyMOLMolecular visualizationNo
AutoDock VinaMolecular dockingNo
RoseTTAFoldStructure predictionYes
GPU-accelerated tools run on HPC infrastructure. Structure predictions for large proteins may take 30-60 minutes.

Visualization

Packages for creating figures and plots:
PackageLanguageBest For
ggplot2RPublication-ready plots, grammar of graphics
matplotlibPythonGeneral purpose, customizable
seabornPythonStatistical visualizations
plotlyR/PythonInteractive plots
ComplexHeatmapRAdvanced heatmaps, annotations

Reference Genomes

Pre-indexed reference genomes available:
OrganismAssemblies
HumanGRCh38 (hg38), GRCh37 (hg19)
MouseGRCm39 (mm39), GRCm38 (mm10)
RatmRatBN7.2
ZebrafishGRCz11
DrosophilaBDGP6
C. elegansWBcel235
YeastR64
E. coliK-12 MG1655
For organisms not listed, you can provide your own reference FASTA file. Biomni will index it automatically.

Requesting New Resources

Don’t see a tool you need? Request it:
  1. Click the chat icon in the bottom-right corner
  2. Describe the tool and your use case
  3. Our team evaluates requests weekly
Popular requests are prioritized for addition.