Characterization of Signaling Pathways in Solid Tumors Using Comprehensive Genomic Profiling

Data Curation, Integration And Harmonization

Transcriptomics Data Analysis And Pipelines

Tools Enabling Data Scaling & Analytics Platforms

A Webinar on Unlocking New E3 Ligases for Targeted Protein Degradation in Cancer Therapy

Diving into Strand's Spatial Transcriptomics Pipeline

An Automated Variant Verification System To Improve Reporting Efficiency

Interpretation of neurological disorders cohort through in-house developed tool, festiVAR, showed an improved diagnostic yield: data from over 1000 Indian patients

Automation Of Time-Consuming WES Steps And Use Of LLMs

Double the Data, Double the Discovery: Hunting Publicly Available and Generated Transcriptomes

Strand’s Metadata Curation Portal: Leveraging Public Data to Drive Precision Research

Navigating Genetics of Dementia in the Indian Subcontinent

Unlocking New E3 Ligases for Targeted Protein Degradation in Cancer Therapy

Studying the Spatio-temporal Root Cell Development of Arabidopsis Using Single-Cell RNA-Seq

Solutions for Bioinformatics Analysis: scRNA-Seq Methylation/Epigenomics, CyTOF

Decoding Data Challenges in Diagnostics: Strand’s Solutions

FDA Rule on Lab Developed Tests (LDTs) for Laboratories Setting Up Molecular LDTs

Driving circRNA Analysis with Strand’s Solutions

Unlocking Untapped Potential: Addressing Current Challenges in Targeted Protein Degradation

Streamlining Germline Testing: Pipeline Development and Clinical Variant Interpretation

Comprehensive End-to-End Solutions for a Pet NGS Diagnostic

Streamline Your Data with Our Expert Wrangling Services

Engineering Excellence: Custom Solutions for Your Needs

Exploring the Hidden Patterns: Leveraging FrAnaTk for cfDNA Fragment Analysis

StrandIris: Revolutionizing Precision Oncology through Enhanced Tertiary Analysis Features

Spatial Transcriptomics: Integrating Imaging, Omics and Clinical Metadata to Enable Discovery

Showcasing Strand’s Expertise: A Closer Look at StrandOmics

Why StrandIris?

Highlighting the Expertise Behind StrandOmics: Advancing Germline and Somatic Variant Classification

Spatial Transcriptomics Data Analysis Pipeline for Research and Diagnostics

Spatial Transcriptomics Workflow for Integrated Analysis and Precise Cell-type Annotations

Decoding Ulcerative Colitis at the Cellular Level with our Single-Cell RNA Sequencing Data Curation Portal

Unlocking Insights: Seamless Data Ingestion, Harmonization, and Curation for Multiomics Datasets with Integrated Ontologies

Cloud Storage & Data Management Strategy for NovaSeq X+ Data

Optimizing Methylation Pipeline: Migration from Snakemake to Nextflow and Deployment on Seqera Platform for Efficiency and Cost Benefits

Target/Biomarker Validation from Omics Data

Strand is Spearheading Pet NGS Diagnostics

Strand’s Data Harmonization Process

Strand’s qPCR Reporting Software (PQRS)

Workflow Management Systems: Our Software Solutions using Nextflow and Snakemake

Strand-Agilent Mass Profiler Professional

Spatial Transcriptomics: Our Path to 10X Genomics Visium Certification

Somatic Variant Database Curation

Ground Truth Dataset Curation for a Major Diagnostics Company

Data Harmonization for a Big Pharmaceutical Company

A Saliva-based Liquid Biopsy Assay for Oral Cancer

Strand's qPCR Reporting Software

Provider Portal & Electronic Data Capture Portal

NGS Analysis Pipeline Development