Unseen, Yet Inherited: Why Fragile X Carrier Testing Should Be Standard in Preconception Care
- Articles, Strand RDRH
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Tumor-Normal Matched Sequencing improves the accuracy and actionability of Liquid Biopsies
- Articles, Strand Oncology
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Hybrid Sequencing: The Future of Accurate and Complete Genome Assembly
- Articles, Multiomics Services
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Single Gene, Hotspot, or CGP? Selecting the Right Molecular Test in Oncology
- Articles, Strand Oncology
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Array vs NGS Technologies for Transgenic Crop Research in Agriculture
- Articles, Multiomics Services
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Improving Hereditary Cancer Detection with NGS + Digital MLPA
- Articles, Strand Oncology
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Microarray vs. NGS for DNA Methylation Patterns:A Comparative Insight
- Articles, Multiomics Services
- Posted on
Cardiovascular Diseases in India: A Silent Genetic Threat
- Articles, Consumer Genomics
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Unmasking Silent Threats: Genetic Mutations and Sudden Cardiac Events
- Articles, Consumer Genomics
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Why is Genomics Key to the Future of Preventive Healthcare?
- Articles, Consumer Genomics
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Lung Cancer Panel – Top 5 Questions Oncologists Need to Know
- Articles, Consumer Genomics
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What is Pharmacogenomics? | फार्माकोजेनोमिक्स क्या है?
- Articles, Consumer Genomics
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dd-cfDNA — The Alphabet Soup of Transplant Rejection Detection
- Articles, Multiomics Services
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Ultrasensitive Detection of Tumour-Specific Mutations in Saliva of Patients With Oral Cavity Squamous Cell Carcinoma
- Articles, Multiomics Services
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Case Study: Patients with variants that are not officially ‘clinically actionable’
- Articles, Multiomics Services
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Recommending Targeted Therapies for Patients with Multiple Variants: A Case Study
- Articles, Multiomics Services
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StrandIRIS: Automated Interpretation of Somatic Variants in more than 500 Genes
- Articles, Multiomics Services
- Posted on
AiArthritis — Autoimmune and Auto-Inflammatory Arthritis
- Articles, Multiomics Services
- Posted on