Knowledge Hub

Exome-Plus in the Detection of Early Onset Bone Marrow Failure

Case Studies, RDRH
Posted on 5 September, 2025

Unseen, Yet Inherited: Why Fragile X Carrier Testing Should Be Standard in Preconception Care

Articles, Strand RDRH
Posted on 31 July, 2025

Sequencing

Tumor-Normal Matched Sequencing improves the accuracy and actionability of Liquid Biopsies

Articles, Strand Oncology
Posted on 23 July, 2025

Germline, Liquid Biopsy, Sequencing

Characterization of Signaling Pathways in Solid Tumors Using Comprehensive Genomic Profiling

Posters
Posted on 21 July, 2025

Oncology

Evidence-Driven Reclassification of VUS: Impact on Genetic Counseling and Surveillance

Case Studies, Oncology
Posted on 21 July, 2025

Patient Awareness Resources

Posters
Posted on 15 July, 2025

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

White Papers
Posted on 15 July, 2025

Hybrid Sequencing: The Future of Accurate and Complete Genome Assembly

Articles, Multiomics Services
Posted on 11 July, 2025

Genetics, Next Generation Sequencing (NGS)

Single Gene, Hotspot, or CGP? Selecting the Right Molecular Test in Oncology

Articles, Strand Oncology
Posted on 30 June, 2025

Next Generation Sequencing (NGS), Oncology

When BRCA Isn’t the Driver: The Case for Comprehensive Genomic Profiling

Articles, Strand Oncology
Posted on 30 June, 2025

BRCA

An analysis of likely germline events by tumor tissue testing on large somatic panels.

Publications
Posted on 29 May, 2025

Oncology

A minimal comprehensive somatic panel to aid clinical decision making in a low cost setting.

Publications
Posted on 28 May, 2025

Oncology

How Millets Talk to Fungi: A Transcriptomic Perspective

Research, Webinars
Posted on 26 May, 2025

research

Evaluating Methylation Signatures: Principles, Techniques, Targeted Methylome Panels, and Methylation Arrays

Research, Webinars
Posted on 26 May, 2025

research

Unlocking CAR T-Cell Innovation: How CITE-seq is Revolutionizing Immunotherapy Research

Research, Webinars
Posted on 26 May, 2025

research

Array vs NGS Technologies for Transgenic Crop Research in Agriculture

Articles, Multiomics Services
Posted on 9 May, 2025

Genetics, Next Generation Sequencing (NGS)

HRD Testing: From Genomic Instability to Impactful Clinical Decision-Making

Articles, Strand Oncology
Posted on 8 May, 2025

Oncology

Improving Hereditary Cancer Detection with NGS + Digital MLPA

Articles, Strand Oncology
Posted on 6 May, 2025

Understanding Autism Spectrum Disorder: From Genetics to Emerging Therapies

Articles, Strand RDRH
Posted on 25 April, 2025

rdrh

The Importance of Genetic Counseling in Cancer Genetics: A Key Tool for Prevention and Care

Articles, Strand Oncology
Posted on 4 April, 2025

Oncology

Key Insights from 1200+ Strand HRD Reports

Posters
Posted on 24 March, 2025

Oncology

Strand Life Sciences: Unlocking Millet-Fungi Symbiosis

Posters
Posted on 22 March, 2025

research

Genetics of Lynch Syndrome and Clinical Implications

Articles, Strand Oncology
Posted on 13 March, 2025

Oncology

Rare Neurometabolic Disorder: Investigating Leigh Syndrome with SURF1 Gene Mutations

Case Studies, RDRH
Posted on 23 February, 2025

The Importance of HRD Testing Over BRCA1/2 for PARP Inhibitor Therapy (Intl)

Case Studies, Oncology
Posted on 23 February, 2025

NGS for Adventitious Agent Screening

Articles, Multiomics Services
Posted on 21 February, 2025

Navigating BRCA1 VUS in High-Grade Serous Peritoneal and Endometrial Carcinomas

Case Studies, Oncology
Posted on 19 February, 2025

United by Unique: A Global Collaboration for Tailored Cancer Solutions

Strand Oncology, Webinars
Posted on 14 February, 2025

Mito Matters: The Importance of Mitochondrial DNA

Articles, Strand RDRH
Posted on 10 February, 2025

rdrh

Revealing Hidden Microbial Diversity Through NGS Technology

Research, Webinars
Posted on 31 January, 2025

research

The Transformative Impact of Next-Generation Sequencing (NGS) in Oncology

Articles, Strand Oncology
Posted on 23 January, 2025

Oncology

Microbial Mysteries: Innovative Approaches to Analysis

Articles, Multiomics Services
Posted on 8 January, 2025

research

Integrating Genomic Testing for Cancer in Gynecological Care- Advancing Preventive Cancer Screening

Strand Oncology, Webinars
Posted on 21 December, 2024

Microarray vs. NGS for DNA Methylation Patterns:A Comparative Insight

Articles, Multiomics Services
Posted on 29 November, 2024

Harnessing the Power of RNA Sequencing

Articles, Multiomics Services
Posted on 27 November, 2024

Carrier Screening – Science, Ecomic or Commerce?

Strand RDRH, Webinars
Posted on 24 November, 2024

Integrating Genomic Testing for Cancer in Gynecological Care: Endometrial Cancer

Strand Oncology, Webinars
Posted on 9 November, 2024

Navigating Fetal Health – Insights into Aneuploidy and IUGR

Strand RDRH, Webinars
Posted on 30 October, 2024

Current Approaches to Surgical Management of Breast Cancers

Strand Oncology, Webinars
Posted on 29 October, 2024

Integrating Genomic Testing Cancer in Gynecologic Care – Breast and Ovarian Cancer

Strand Oncology, Webinars
Posted on 25 October, 2024

Homologous Recombination Deficiency in Ovarian Cancer: Current Approaches and Future Prospects

Articles, Strand Oncology
Posted on 22 October, 2024

Oncology

Understanding Hereditary Testing for Risk Management

Articles, Strand Oncology
Posted on 22 October, 2024

Oncology

CME On HRD

Strand Oncology, Webinars
Posted on 15 October, 2024

Building methylation workflows for the clinic: A Strand Life Science Perspective

Research, Webinars
Posted on 10 October, 2024

research

Lethal Serpinopathy

Strand RDRH, Webinars
Posted on 5 October, 2024

Comprehensive RNA-seq Analysis in Strand NGS

Research, Webinars
Posted on 27 September, 2024

research

Fetal Autopsy- Know more on Whys & What it is

Strand RDRH, Webinars
Posted on 11 September, 2024

SMA Awareness Genetic Testing and Management in collaboration with MRDS & SMA malaysia association

Strand RDRH, Webinars
Posted on 7 September, 2024

Harnessing RNA Seq for Functional Insights

Research, Webinars
Posted on 31 August, 2024

research

5 Applications of miRNA Research: A Deeper Dive

Articles, Multiomics Services
Posted on 23 August, 2024

Prenatal Echogenic Mysteries Genetics of Brain flicks, Bright Bowel, Shiny Kidneys and Heart

Strand RDRH, Webinars
Posted on 22 August, 2024

Strand CME – Lab Capabilities with (Warith International Cancer Institute)

Strand Oncology, Webinars
Posted on 12 August, 2024

Decoding Rare Diseases with Whole Exome Sequencing

Strand RDRH, Webinars
Posted on 6 August, 2024

Role of Genetic Counselling In Pediatric Neurological Disorders with Case Studies

Strand RDRH, Webinars
Posted on 6 August, 2024

HRD Demystified

Strand Oncology, Webinars
Posted on 3 August, 2024

Webinar on IVF (World IVF Day – Genes, Gametes and Emryos)

Strand RDRH, Webinars
Posted on 25 July, 2024

Clinical Genetics in Pediatrics

Strand RDRH, Webinars
Posted on 18 July, 2024

Is it Cerebral Palsy?

Strand RDRH, Webinars
Posted on 11 July, 2024

Basics of interpretation of HPLC and Prenatal Diagnosis of Hemoglobinopathies

Strand RDRH, Webinars
Posted on 7 July, 2024

Multinational Panel Discussion: Rare Chromosome Disorders Awareness

Strand RDRH, Webinars
Posted on 29 June, 2024

Sickle Cell Anemia Awareness Day and Hemoglobinopathies: What is New for OBGYN Practitioners

Strand RDRH, Webinars
Posted on 19 June, 2024

Role of Genetics in Epilepsy

Strand RDRH, Webinars
Posted on 23 May, 2024

Decoding Rare Diseases with Whole Exome Sequencing

Strand RDRH, Webinars
Posted on 21 May, 2024

NIPS (Non-Invasive Prenatal Screening): The Use and the Misuse

Strand RDRH, Webinars
Posted on 13 May, 2024

Understanding Ovarian Cancer: Risks, Symptoms, and Prevention: Whispers Defy Numbers

Articles, Strand Oncology
Posted on 8 May, 2024

Oncology

Autism: Prevention, Therapy & Cure

Strand RDRH, Webinars
Posted on 24 April, 2024

Spinal Muscular Atrophy Awareness Month Webinar

Strand RDRH, Webinars
Posted on 26 February, 2024

Low Pass Genome Sequencing (LPGS) an NGS based Chromosomal Analysis

Strand RDRH, Webinars
Posted on 22 February, 2024

Enhancing Fetal Care: The Role of Genetic Testing

Strand RDRH, Webinars
Posted on 9 February, 2024

HRD and PARP Inhibitors: A Promising Treatment Approach

Articles, Strand Oncology
Posted on 4 February, 2024

Oncology

Cardiovascular Diseases in India: A Silent Genetic Threat

Articles, Consumer Genomics
Posted on 15 December, 2023

Unmasking Silent Threats: Genetic Mutations and Sudden Cardiac Events

Articles, Consumer Genomics
Posted on 14 December, 2023

Genetic Testing: Your Personalized Path to Wellness

Articles, Consumer Genomics
Posted on 9 November, 2023

1st Strand Connect International Panel Discussion on Therapeutic Utility of HRD in Ovarian Cancer

Strand Connect International Panel Discussion, Webinars
Posted on 29 July, 2023

Why is Genomics Key to the Future of Preventive Healthcare?

Articles, Consumer Genomics
Posted on 3 April, 2023

Chris Hemsworth & The Risk of Alzheimer’s Disease

Articles, Consumer Genomics
Posted on 27 March, 2023

Lung Cancer Panel – Top 5 Questions Oncologists Need to Know

Articles, Consumer Genomics
Posted on 27 January, 2023

What is Pharmacogenomics? | फार्माकोजेनोमिक्स क्या है?

Articles, Consumer Genomics
Posted on 20 January, 2023

Covid Treatments: New Uses of Old Pills

Articles, Multiomics Services
Posted on 1 December, 2022

Lynch syndrome: An unusual case of familial cancer unearthed

Publications
Posted on 14 April, 2022

Oncology

Don’t Blame Your Genes

Articles, Consumer Genomics
Posted on 18 March, 2022

dd-cfDNA — The Alphabet Soup of Transplant Rejection Detection

Articles, Multiomics Services
Posted on 23 February, 2022

First Successful Pig Heart Transplant

Articles, Multiomics Services
Posted on 31 January, 2022

Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families

Publications
Posted on 7 January, 2022

Cancer mRNA Vaccines

Articles, Strand Oncology
Posted on 6 January, 2022

Assessing Utility of Clinical Exome Sequencing in Diagnosis of Rare Idiopathic Neurodevelopmental Disorders in Indian Population.

Publications
Posted on 23 December, 2021

rdrh

mRNA Vaccines: Back to the Basics

Articles, Multiomics Services
Posted on 17 November, 2021

World Hepatitis Day

Articles, Multiomics Services
Posted on 5 November, 2021

Determining Cost-Optimal Next-Generation Sequencing Panels for Rare Disease and Pharmacogenomics Testing.

Publications
Posted on 8 August, 2021

rdrh

Validation of whole genome sequencing from dried blood spots

Publications
Posted on 20 April, 2021

rdrh

Targeted Sequencing Detects Variants That May Contribute to the Risk of Neuropsychiatric Disorders

Publications
Posted on 25 March, 2021

rdrh

Why Aren’t All Blue Whales Ridden with Cancer?

Articles, Strand Oncology
Posted on 15 February, 2021

Ultrasensitive Detection of Tumour-Specific Mutations in Saliva of Patients With Oral Cavity Squamous Cell Carcinoma

Articles, Multiomics Services
Posted on 14 January, 2021

Ultrasensitive detection of tumor-specific mutations in saliva of patients with oral cavity squamous cell carcinoma

Publications
Posted on 6 January, 2021

Oncology

Liquid Biopsies: Non-Invasive Cancer Detection

Articles, Strand Oncology
Posted on 5 January, 2021

Strand Life Sciences’ DNA Testing Plans

Articles, Consumer Genomics
Posted on 2 January, 2021

Landscape of clinically actionable mutations in breast cancer ‘A cohort study

Publications
Posted on 1 January, 2021

Oncology

Turning Evolution on Its Head

Articles, Multiomics Services
Posted on 31 December, 2020

Case Study: Patients with variants that are not officially ‘clinically actionable’

Articles, Multiomics Services
Posted on 18 December, 2020

Recommending Targeted Therapies for Patients with Multiple Variants: A Case Study

Articles, Multiomics Services
Posted on 9 December, 2020

Single Cell Transcriptomics

Articles, Multiomics Services
Posted on 18 November, 2020

The Story of Osimertinib

Articles, Multiomics Services
Posted on 10 November, 2020

Data Analysis in Rare Disease Diagnostics

Publications
Posted on 20 October, 2020

rdrh

Breast Cancer: Choosing Facts Over Myths

Articles, Consumer Genomics
Posted on 19 October, 2020

Lethal Cenani Lenz syndrome in two consecutive pregnancies: Further extension of phenotype from Maldives

Publications
Posted on 17 October, 2020

rdrh

Darwinian Evolution and Cancer Treatment

Articles, Multiomics Services
Posted on 8 October, 2020

Genotype-phenotype correlates of infantile-onset developmental & epileptic encephalopathy syndromes in South India: A single centre experience

Publications
Posted on 1 October, 2020

rdrh

StrandIRIS: Automated Interpretation of Somatic Variants in more than 500 Genes

Articles, Multiomics Services
Posted on 16 September, 2020

Synaptic Nuclear Envelope Protein 1 (SYNE 1) Ataxia with Amyotrophic Lateral Sclerosis-like Presentation: A Novel Synaptic Nuclear Envelope Protein 1 (SYNE 1) Gene Deletion Mutation from India

Publications
Posted on 16 July, 2020

rdrh

Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology

Publications
Posted on 6 July, 2020

Oncology

Lipoprotein Lipase Deficiency

Publications
Posted on 30 May, 2020

rdrh

AiArthritis — Autoimmune and Auto-Inflammatory Arthritis

Articles, Multiomics Services
Posted on 15 May, 2020

Development of a Low-cost NGS Test for the Evaluation of Thyroid Nodules

Publications
Posted on 20 November, 2019

Oncology

Life In The Time Of Genetic Decoding

Articles, Consumer Genomics
Posted on 10 November, 2019

Homozygous sequestosome 1 ( SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy

Publications
Posted on 16 September, 2019

rdrh

Targeted sequencing of the DMD locus: A comprehensive diagnostic tool for all mutations

Publications
Posted on 1 September, 2019

rdrh

Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2

Publications
Posted on 10 July, 2019

rdrh

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients

Publications
Posted on 8 May, 2019

rdrh

Incidental Finding of Lynch Syndrome Role of Genetic Counselling

Publications
Posted on 25 April, 2019

Oncology

Analysis of solid tumor mutation profiles in liquid biopsy

Publications
Posted on 29 August, 2018

Oncology

Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent

Publications
Posted on 11 April, 2018

rdrh

Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing

Publications
Posted on 1 April, 2018

rdrh

Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations.

Publications
Posted on 22 February, 2018

Oncology

Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia

Publications
Posted on 1 February, 2018

Genotype-Phenotype Analysis in an Indian Family Affected with Li-Fraumeni Syndrome-Role of Genetic Counselling

Publications
Posted on 4 September, 2017

Oncology

Incidental Findings in Male Breast Carcinoma: A Genetic Counseling Approach

Publications
Posted on 4 September, 2017

Oncology

A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia

Publications
Posted on 11 July, 2017

Oncology

Clinical and genetic analysis of Indian patients with NDP-related retinopathies

Publications
Posted on 10 June, 2017

rdrh

Strand Advantage test for early-line and advanced-stage treatment decisions in solid tumors

Publications
Posted on 19 January, 2017

Oncology

Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss

Publications
Posted on 22 September, 2016

rdrh

Homozygosity mapping guided next generation sequencing to identify the causative genetic variation in inherited retinal degenerative diseases

Publications
Posted on 7 July, 2016

rdrh

Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort

Publications
Posted on 1 April, 2016

Oncology

Identification of a novel glucokinase mutation in an Indian woman with GCK-MODY

Publications
Posted on 1 April, 2016

Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India

Publications
Posted on 25 February, 2016

Oncology

Recurrent  and novel  GLB1 mutations  in  India.  Gene

Publications
Posted on 10 August, 2015

Sample preparation method considerations for integrated transcriptomic and proteomic analysis of tumors

Publications
Posted on 6 August, 2015

Oncology

Release of (and lessons learned from mining) a pioneering large toxicogenomics database

Publications
Posted on 12 June, 2015

research

Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease

Publications
Posted on 2 April, 2015

Evaluation of quantitative miRNA expression platforms in the microRNA quality control (miRQC) study

Publications
Posted on 29 June, 2014

research

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge

Publications
Posted on 25 March, 2014

rdrh

Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency

Publications
Posted on 25 October, 2012

rdrh

Bortezomib enhances the efficacy of fulvestrant by amplifying the aggregation of the estrogen receptor, which leads to a proapoptotic unfolded protein response