Work backward from target compounds and candidates
Connect disease context, existing data, imaging, omics, and structural indicators to define the efficacy, toxicity, and mechanism conditions to explore.
Integrate Analysis System IAS
IAS is not a replacement for every point tool. It is a web-based workflow layer that brings fragmented research data, analysis procedures, review records, and report creation into the same context.

IAS does not replace modality-specific tools. It connects experiment-level data, analysis, review, and reporting into one decision surface.
Organize imaging, flow, genomics, mass spectrometry, and molecular structure outputs by experiment.
Handle modality-specific analysis methods in the same workspace and reduce manual handoffs.
Tie multiple assay results into one research decision so comparison and interpretation move faster.
Carry analysis history, checks, and report creation toward reproducible final outputs.
IAS organizes target compounds, candidate drugs, hypotheses, evaluation metrics, and next conditions so analysis results can shape simulation and experimental planning before the next run.
Beyond improving analysis accuracy, interpretation, and reporting efficiency, IAS raises experiment-design quality and shortens the research cycle from candidate discovery to wet validation.
Connect disease context, existing data, imaging, omics, and structural indicators to define the efficacy, toxicity, and mechanism conditions to explore.
Feed promising conditions, comparison groups, and measurement parameters into the next in silico review or wet-lab plan so trial order becomes clearer.
Screen out lower-promise conditions earlier and focus experiments, checks, and reviews where they matter, reducing effort in both analysis work and wet-lab research.
NEW FEATURE
Helping researchers summarize, interpret, and draft reports from complex analysis results through natural language instructions.
LifeAnalytics IAS now supports ChatGPT and LifeAnalytics' proprietary generative AI application. Using research data, analysis history, experiment records, analysis summaries, and report context, IAS helps researchers summarize, interpret, create reports, and draft scientific manuscripts from complex life science analysis results.
IAS supports multiple analysis areas including image analysis, gene analysis, flow cytometry, mass spectrometry, molecular structure analysis, spatial multi-layer multi-omics analysis, and integrated analysis.

IAS centrally manages representative research data such as image analysis, flow cytometry, next generation sequencing, molecular structure, and mass spectrometry in the cloud.
Visualization, alignment, assembly, and annotation of DNA and protein sequences.
Acquisition, processing, and analysis of mass spectrometry data, including metabolomics.
High-accuracy prediction of 3D protein structure from amino acid sequences.
AI-assisted discussion reports based on individual analysis results.
Image analysis for cells and tissue sections, including 3D, Timelapse, HCS, and pathology.
Flow cytometry analysis such as SPADE, U-MAP, and dot plots.
IAS specification details
Handle imaging, flow cytometry, genomics, mass spectrometry, molecular structure, and integrated analysis in one research workbench.
IAS is not a single image-analysis application or a collection of isolated point tools. It brings imaging, flow cytometry, genomics, mass spectrometry, molecular structure analysis, integrated analysis, and data management into one research workbench experience.
IAS AI output does not guarantee clinical diagnosis. Interpretation of pathology images, medical images, genomics, molecular structure, and mass-spec results should be combined with specialist review, raw-data inspection, standard methods, and external validation.
Each card summarizes inputs, outputs, and review points at a practical evaluation level.
Long model inventories are grouped by purpose so readers can see how each model is used and what should be checked before interpreting outputs.
IAS imaging modes cover Tissue, Cell, Material, Semicon, Animal, and ML workflows so teams can choose models by purpose.
TissueNet, Foxp3 Spatial, Foxp3 DAB Spatial, Ki67-Br, Pathology, CT/MRI Segment, Spatial Omics, TissueNT2, Thyroid, and Lymph support tissue segmentation, ROI quantification, positivity review, spatial distribution, and multi-channel statistics.
Cyto, Cyto2, SAM, 2Dtracker, 3Dtimelapse, Nuclei, Nucleus01, Confluency, CM-CellCycle, LiveCell, CP, CPx, TN1-3, LC1-4, Single Cell Protein, 3DVD, LFcell02, and CellPaintingV3 support cell segmentation, tracking, morphology profiling, localization, and state review.
Pore Analysis, Layer, Microridge, Mfiber1, Mfiber2, Wafer, Mouse Dynamics Tracking, and Pixel Classification support pore, layer, ridge, fiber, wafer, animal motion, and user-defined pixel-classification reviews.
Pathology mode combines local pathology processing, ROI editing, vision-language assistance, visual similarity, and nuclei/cell segmentation support.
OpenSlide, tifffile, OpenCV, and LAB/HSV/RGB Magic Wand support tissue masks, tile heatmaps, overlays, and color-space ROI editing.
Qwen2.5-VL + LoRA assist, ResNet152 visual similarity, and DeepLIIF biomarker support help generate descriptions, hypotheses, similar-image candidates, and biomarker-support summaries.
checkpoint-gated tumor segmentation, StarDist H&E nuclei, Cellpose-SAM service, and InstanSeg service provide candidate segmentation for tumor regions, nuclei, and cells.
This is not a diagnostic function. Outputs are research and review support for specialist-led pathology review.
IAS connects FCS input, compensation, QC, gates, embedding, clustering, statistics, and reporting.
Compensation, spectral unmixing, PeacoQC, DataQC, doublet checks, and margin checks help review spillover, spectral overlap, abnormal events, flow-rate drift, doublets, and margin events.
Gate editor, Boolean gates, UMAP, t-SNE, opt-SNE, and viSNE help preserve manual thresholds and inspect high-dimensional cytometry data.
FlowSOM, SPADE, CITRUS, population statistics, and marker summaries support population comparison, MFI review, figures, and reports.
Embeddings are visualizations; interpretation should be checked against marker expression and manual gates.
IAS organizes sequence similarity, alignment, variants, single-cell analysis, reference mapping, and multi-omics evidence by experiment.
BLAST, MSA, Phylogeny, CRISPR, QC & Alignment, Variant Calling, Joint Genotyping, and Annotation connect sequence review to variant and annotation review.
Genome Browser and Single-cell Async support genomic-region inspection, variants, gene models, normalization, HVG, PCA, clustering, UMAP, and marker detection.
Harmony, scGPT, cell annotation capability checks, and Multi-Omics connect batch correction, reference mapping, cell-type annotation candidates, expression, variants, phenotypes, and other modes.
Check genome build, QC, depth, population frequency, labeled references, batch effects, missingness, and unit alignment.
IAS connects raw/mzML/mgf/wiff inputs to peak features, identification, quantification, QC, database matching, reports, and multi-omics.
MS-DIAL, XCMS, MZmine, MS-FINDER, MS-CleanR, LipidSearch, and LipidBlast outputs are organized for candidate review and quantification.
MaxQuant, Proteome Discoverer, FragPipe, Mascot, Byonic, Spectronaut, DIA-NN, OpenSWATH, Prosit, SCiLS Lab, Cardinal, MSiReader, METASPACE, and OpenMSI outputs can be reviewed as part of the same workflow.
MRM/SRM/PRM, MRMProbs, DeepNovo, Spec2Vec, MS2DeepScore, AlphaPept, mixOmics, MOFA(+), DIABLO, and OmicsNet outputs can be tied back to research decisions.
AI candidates should be verified with database matching, standards, MS/MS evidence, FDR, QC, blanks, and batch correction.
IAS helps review the path from Sequence/PDB/Ligand to structure prediction, docking, MD, validation, and reports.
Monomer and complex structure prediction, public structure retrieval, and pLDDT/PAE review are handled as review inputs.
GNINA, AutoDock-family, LightDock path, OpenMM, and mdtraj support binding-pose candidates, scores, binding-site review, RMSD/RMSF, interactions, and solvent-condition review.
Validation quality checks, reports, function annotation, spectrum prediction, knowledge graph, QM, and FEP scaffolds help organize quality and extension candidates.
Check confidence, pLDDT/PAE, protonation, box, charge, ligand preparation, force field, solvent, temperature, and simulation length.
IAS connects imaging, genomics, mass spec, flow cytometry, molecular structure, and reports around a consistent sample ID.
sample ID and provenance mapping connect sample IDs, experiments, files, and preprocessing history across modes.
compute-statistics, random-effects meta-analysis, and cross-modal review connect effect sizes, confidence intervals, heterogeneity, imaging features, gene expression, metabolites, and population ratios.
Gen Report, report history, evidence maturity, DB Manage, and Sample DB help preserve report context, input history, file references, mode estimation, and re-analysis paths.
For clinical research support, keeping the same sample ID across Imaging, Genomics, MassSpec, and FlowCyto is critical.
Support functions reduce uncertainty during analysis by connecting operation guidance, knowledge search, ROI questions, and help dialogs.
Support Chat connects operation guidance, inquiry handoff, knowledge search, and AI-answer support for Imaging, Genomics, FlowCyto, Molecular, MassSpec, and Integrate.
Patho Chat combines ROI crops, feature extraction, similarity candidates, and Qwen-family LLM support to provide finding candidates, differential candidates, and suggested checks under pathology-specialist review.
Q&A icons and Help screens reduce operation mistakes through tooltips, Quick Start, Help dialogs, shortcut explanations, and Support Chat / Patho Chat visibility controls.
Patho Chat does not replace pathology review. Outputs are confirmation support and hypothesis-generation support for selected ROIs.
Your target data, analysis problem, and evaluation timing do not need to be fully organized. We can review the appropriate analysis modes and implementation path with you.
Demo consultationAnalytical methods for fundamental research are unified so researchers can work in the same environment with reproducible workflows.

We support additional proprietary AI and analysis features tailored to your goals, helping automate the entire research process.


Manage data, analysis, and reports in one web system.

Use the same analysis platform in collaborative and remote environments without local installation.

Smoothly proceed with questions and checks during analysis work.

Designed for compatibility with data management, leak prevention, and regulatory needs.

Support discovery of notable points from images and analysis results.

Supports integration of many data formats used in research settings.
Specialized analysis procedures can be shared more easily, improving reproducibility in remote collaboration.
Central management of multiple data formats reduces the time required for analysis and reporting.
Instead of a long extension list, representative formats are grouped by research workflow and data type. For formats not shown here, share example files, instrument names, and desired outputs.
Please contact us for formats not listed above.

Support data management that considers regulatory requirements such as 21 CFR Part 11.

Visualization tools help researchers inspect analysis results intuitively.

Support report and manuscript draft creation from analysis results.

Connect analysis, management, and reporting to improve the entire lab workflow.
Each card separates the input data, the outputs IAS organizes, and the research decision it supports. Flow Cytometry, NGS, Molecular Structure, and MassSpec are treated as first-class analysis modes alongside Imaging.

Image analysis and Cell Painting
Extract morphology, organelle, and cluster features from cell images and connect them with disease context and known compound tendencies.

Immune cells, cell therapy, and quality control
Organize FCS gating, population ratios, and abnormal population comparisons for cell therapy, immune analysis, and reporting workflows.

Genomics, RNA-seq, and clinical research
Bring sequence outputs, variant candidates, expression changes, and sample context into a single review surface with other assay results.

Proteins, materials, and structural evaluation
Manage 3D structures, segmented regions, features, and candidate models so structural differences and regions of interest are easier to compare.
Metabolites, quality evaluation, and component comparison
Manage spectra, peaks, sample conditions, and comparison groups to support component review, quality differences, and reporting.