AI-NATIVE BIOLOGY WORKSPACE

Model life.Decode disease.

MindCell brings virtual cell modeling, disease phenotype intelligence, and specialized biomedical AI into one agent-orchestrated research environment.

  • + Agent-routed
  • + Model-aware
  • + Traceable
Detailed virtual cell modelA living cell with a nucleus, mitochondria, endoplasmic reticulum, Golgi apparatus, lysosomes, ribosomes, and animated molecular signals.MITOCHONDRIAATP flux 8.42CELL STATEvector 12,842PERTURBATIONshift +0.73
LIVE IN-SILICO RESPONSE
06organelles modeled
SCROLL TO DISCOVER
AI-NATIVE DRUG DISCOVERY

From AI disease modeling
to drug discovery.

Build a computable disease model across organism, cell, and molecule—then use the same biological model to screen interventions and identify therapeutic targets.

01Build the disease modelPHENOTYPE · CELL · MECHANISM
Comparison of a healthy brain and a brain affected by Alzheimer's diseaseLAYER / 01 RESOLVED
Organism

Disease phenotype

Resolve the anatomical and functional signatures that distinguish disease from health.

Comparison of a healthy neuron and a degenerating neuronLAYER / 02 RESOLVED
Cell

Cellular phenotype

Trace tissue-level change to the cell states, morphology, and functions that drive it.

Diagram of amyloid precursor protein processing and amyloid beta productionLAYER / 03 RESOLVED
Molecule

Molecular mechanism

Connect cellular dysfunction to actionable pathways, proteins, and molecular events.

02Turn the model into discoveryMODEL · SCREEN · PRIORITIZE
STAGE 01MODEL
MODELACTIVE

AI disease modeling

Build a computable disease model from multimodal phenotype and patient evidence.

+ MULTIMODAL+ CAUSAL
STAGE 02SCREEN
HIT02

Cellular drug screening

Run in-silico perturbations and prioritize compounds by phenotype rescue, not proxy alone.

+ PERTURB+ RANK
STAGE 03TARGET

Target identification

Surface intervention points linked to mechanism, predicted response, and supporting evidence.

+ MECHANISM+ EVIDENCE
OUTPUTMechanism-linked therapeutic hypotheses

Traceable from phenotype to target.

FOUNDATION MODELS, ONE WORKSPACE

The model hub for living systems.

Run proven biological AI models through one research interface. MindCell routes your question to the right specialist, keeps inputs and outputs together, and makes every result traceable.

MindCellModel HubROUTED BY AI

AlphaFold 3

Complex structure

Boltz

Structure & affinity

OmegaFold

Single-sequence folding

OpenFold

Open structure platform

DiffDock

Molecular docking

RFdiffusion

Generative design

ProteinMPNN

Sequence design

ProGen2

Protein generation

ESM

Protein language model

Evo 2

Genomic language model

RiNALMo

RNA language model

Uni-Mol

Molecular foundation model

MindCell research blog

Ideas, methods, and evidence.

View all blogs →
01

How to Map Protein Aggregation Propensity with Aggrescan3D and a PDB Structure

Static Aggrescan3D 1.0.2 analysis of the official RCSB Protein Data Bank structure 2GB1 produced finite scores for all 56 residues of chain A. The minimum score was −3.5629, the maximum was 1.1983, and the arithmetic mean was −1.4135875. The highest-scoring residue was valine A:21 at 1.1983; methion

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02

How to Align PDB Protein Structures with PyMOL and Interpret RMSD Correctly

PyMOL 3.1.0 aligned the official RCSB/PDBe 1D3Z ubiquitin NMR structure as the mobile object to the official RCSB 1UBQ X-ray ubiquitin structure as the target. The exact cmd.align return was [0.39735108613967896, 449, 5, 1.2869186401367188, 602, 381.0, 76]: refined RMSD 0.397351 Å across 449 atom pa

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03

How to Reconstruct Ancestral DNA Sequences with ancseq and IQ-TREE

The validated workflow selected the IQ-TREE model from the supplied alignment, rooted the analysis with AVR-Mgk5GE162, reconstructed 13 ancestral records, and produced all six required final deliverables. The sorted state table contained 68,807 bytes of explicit state probabilities; intermediate IQ-

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04

How to Annotate and Number an Antibody Light Chain with ANARCI and Kabat

ANARCI recognized a human kappa light chain spanning residues 0–106. The retained HMM score was 197.0 with an e-value of 1.6 × 10⁻61, and the assigned germlines were IGKV1-1201 and IGKJ101. Both the Kabat-numbered CSV and the HMM evidence table passed semantic validation. This result passed native e

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05

How to Estimate Aqueous Solubility from SMILES with the ESOL Model

The model predicted logS values of −0.0424460527 for ethanol, −1.9325820263 for benzene, and −2.3143366025 for octanol. The expected ordering ethanol benzene octanol was recovered, and the output retained molecular weight, LogP, rotatable bonds, aromatic proportion, SMILES, and units. This result pa

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RESEARCH COLLABORATION

COSINX

Build models with us.

For research partnerships, scientific collaboration, and MindCell enquiries, contact our team directly.

research@cosinx.com