Unlock the full potential of your medical and biological data with
our expert curation services. From radiological imaging to spatial
omics, our tailored solutions deliver organized, annotated, and
high-quality datasets to drive precise diagnostics, accelerate
research, and power innovative discoveries.
Our spatial curation services organize spatial omics data,
preserving molecular and tissue context to reveal critical
biological patterns.
What we do
Normalize and align spatial data, preserving tissue coordinates.
Annotate molecular features and tissue regions (e.g., tumor
boundaries).
Integrate with single-cell or bulk omics for comprehensive
insights.
Optimize data for spatial analysis and visualization platforms.
Applications
Study tissue architecture in cancer, neurobiology, or
development.
Identify spatially restricted disease markers for targeted
therapies.
Enhance drug development with tissue-specific molecular
insights.
Single-Cell Annotation
We process and annotate single-cell omics data (e.g., scRNA-seq)
to reveal cellular diversity, supporting advanced research in
biology and personalized medicine.
What we do
Clean and normalize raw data to remove noise and artifacts.
Annotate cell types using reference atlases like the Human Cell
Atlas.
Integrate datasets across experiments for multi-dimensional
analysis.
Format data for visualization tools like t-SNE or UMAP.
Applications
Uncover cellular diversity in immunology, cancer, and
development.
Identify disease-specific cellular markers for therapeutic
targets.
Support personalized medicine with patient-specific profiles.
Pathology Image Annotation
Our annotation services label histological and cytological images
with precision, transforming microscopy data into actionable
insights for diagnostics and research.
What we do
Preprocess whole-slide images for clarity and consistency.
Label cell types, tissue structures, and pathological changes.
Use standardized ontologies like SNOMED CT for interoperability.
Link images with clinical metadata for contextual analysis.
Applications
Improve diagnostic accuracy for cancer and other diseases.
Enable AI tools for automated pathology analysis.
Accelerate research in biomarker discovery and drug development.
Bulk Annotation
Comprehensive Analysis of Bulk Sequencing Data
We organize and analyze bulk sequencing data (e.g., RNA-seq,
DNA-seq) to deliver structured datasets for large-scale genomic
research.
What we do
Clean, align, and normalize raw sequencing data.
Annotate genes, variants, or functional elements using standard
databases.
Validate data for accuracy and reproducibility.
Format datasets for downstream analytical pipelines.
Applications
Identify disease-associated genes or pathways in genomic
studies.
Support population-level research on genetic diversity.
Enable drug discovery through molecular target identification.
ATAC-Seq Annotation
Tailored Processing for Chromatin Accessibility Studies
Our ATAC-Seq curation services process and annotate data to enable
precise studies of chromatin accessibility and gene regulation.
What we do
Filter, align, and normalize ATAC-Seq data to remove noise.
Annotate accessible chromatin regions (e.g., promoters,
enhancers).
Integrate with transcriptomic or epigenomic data for
comprehensive analysis.
Format data for tools like ChIP-Seq or motif analysis.
Applications
Study gene regulation in development or disease.
Identify epigenetic changes in cancer or neurological disorders.
Support drug development targeting regulatory elements.
Contact Us
Office4445 Eastgate Mall, Suite 200, San Diego, California 92121, USA.
Introduction
What we do
Applications
