Strand’s scRNA Portal
This portal is your gateway to meticulously collected single-cell RNA sequencing data empowering precision research.
This platform offers harmonized single-cell RNA sequencing datasets focused on complex diseases with significant unmet clinical needs, including Ulcerative Colitis, Alzheimer’s Disease, and Frontotemporal Dementia.
Samples
2200 +
Cell Types
100 +
Cells
18M +
Your Data Partner for accessible scRNA sequencing data
We curate publicly available datasets and offer custom curation for datasets of your interest. We harness datasets from public repositories and harmonize them using internationally recognized ontologies and controlled vocabularies to enhance data usability for downstream applications. Each dataset has been curated from NCBI’s GEO platform.
Our mission is to facilitate innovative research by providing accessible, high-quality data that drives precision insights and advances our understanding of complex diseases.
Key features
01
Curation Requests
Submit a dataset of your choice for curation by our expert curation team.
MAKE A REQUEST
02
Datasets
Meticulous metadata curation and harmonization in 3 disease areas, with over 80+ metadata fields spanning 3 levels of curation.
03
Metadata Visualization
Uncover hidden patterns, correlations and trends in the metadata using charts and graphs in various formats.
Metadata Curation
This is a disease-focused portal solving a key challenge in dataset acquisition for biomedical research. We artfully extract datasets from public repositories using customized keywords.
Data is standardized and harmonized using internationally recognized ontologies and vocabularies.
We offer extensive metadata curation with 80+ metadata fields spanning 3 levels of curation: study, experiment, and sample. We can customize metadata fields as needed to provide the right inputs for your research.
The search feature on our portal helps users browse using specific keywords. There are 26 filters to help narrow down to a dataset that meets your requirement.
These datasets can be combined with the Strand Bioinformatics tools that support scRNA sequencing analysis, bulk RNA sequencing and multi ‘omics analysis for valuable holistic insights.
Features of the Database
Custom Keywords To Harness Relevant Datasets
3 Levels Of Curation
80+ Metadata Fields
Standardization Using Recognised Ontologies & Vocabularies
Independent Curation & Review Process
About Strand
Strand Life Sciences is a comprehensive bioinformatics company involved in genomic and transcriptomic research. Our focus is on improving the drug discovery process and precision medicine.
Our team comprises over 300 highly trained curation scientists, software engineers, testing engineers, bioinformaticians, and clinical researchers. We have 23 years of experience in this domain.
We are a Bangalore-based company with close ties with the Bay Area and San Diego, where many of our clientele are based.
