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
