It is a pleasure to share the new publication on the comprehensive genome-scale map of structural variants in #India from whole #genome sequences authored by Mohit Divakar et al. from @SridharSivasub3 Lab at CSIR-IGIB #IndiGen rdcu.be/c57Lg

▶️Can #SARSCoV2 and #Influenza co-infect ? Answer is possibly yes, In this recent preprint, using #genome sequencing, we prove the co-infection was due to BA.4.1 of #omicron and #Influenza A #H3N2 in a 10 year old child from #Kerala

⚠️ BREAKING: Two poultry workers test positive for H5N1 bird flu in the UK 🇬🇧

Our fresh pre-print on "An amplicon-based approach for fast and scalable genome sequencing of lumpy skin disease virus #LSDV on benchtop next-generation sequencers" with #GenePiBoxPox for analysis and interpretation of LSDV Genome, is now online. doi.org/10.21203/rs.3.…

Always a pleasure to hear Vinod Scaria speak on personal genomes to precision medicine. At Illumina genomics innovation roadshow 2023, Delhi CSIR, India CSIR-IGIB Premas Life Sciences

Vinod Scaria speaking on the power of #genomics in precision medicine at The Genomics Innovation Summit organized by Illumina Premas Life Sciences in Delhi

Series of excellent talk on Genomics, Vinod Scaria talking about personal Genomes to precision medicine at #Genomics innovation roadshow 2023 organized by Illumina Premas Life Sciences

The human Y chromosome does much more that just define the biological male of the species. We explain in The Hindu the role of Y Chr in disease, lifespan and what it means to lose the Y Chr. Vinod Scaria @SridharSivasub3 CSIR-IGIB

▶️ Scientists have been aware of cell-free DNA since 1948, but only in the last two decades, with the advent of high-throughout genomics have this knowledge been used in clincial settings. @SridharSivasub3 and I write in The Hindu today thehindu.com/sci-tech/scien…

Our latest research exploring APOE alleles in India and other populations and their implications for #Alzheimers treatment with #lecanemab is now published rdcu.be/dm0em

#Movember is round the corner. Let us talk about #ProstateCancer & #TesticularCancer and of course grow a #moustache in support.

Exciting 3-day 🧬Bioinformatics training at #Mizoram University, Aizawl, with young scientists, Fostering knowledge exchange and collaboration. Empowering the next wave of bioinformatics enthusiasts! with Bani Jolly Anindyajit Banerjee Karkinos Healthcare

We at Karkinos Healthcare conducted an insightful 3-day whole exome sequencing analysis workshop at Mizoram University, amid Aizawl's beauty. Emphasising on reciprocal nature of teaching and learning, covered several key concepts from the basics of NGS to somatic variant calling.

"On World Cancer Day, at #Karkinos Healthcare, we stand united in the fight against cancer, dedicating our efforts to illuminate the path of hope through innovative diagnostics, compassionate care, and unwavering support. Karkinos Healthcare

Reflecting on #WorldCancerDay – a call to embrace early detection, harness #genomics for tailored treatments, and strive for equitable healthcare, breaking barriers in the battle against cancer. Karkinos Healthcare

This #WorldCancerDay, let's also reflect on Henrietta Lacks' story, emphasizing the need for inclusive, accessible, and affordable cancer care, a powerful reminder for informed consent and equitable access to the benefits of scientific research.

Every child deserves a future filled with laughter, dreams, & endless possibilities. Today, we stand together to raise awareness and support for children fighting cancer. Together, we can light up their world with hope and healing. #ChildhoodCancerAwareness #FightWithCourage

🗺️ #BirdFlu / Influenza A H5N1. Bird, Cattle and Human infections. What we know and what we don't . Should we be worried ? A short🧵with explainer .

1-2 in 1000 children suffer from hearing loss at birth, significantly contributed by genetic defects in over a dozen genes. Gene therapy could offer them a promise for sound future. RAHUL BHOYAR and I write in The Hindu Read the full text here epaper.thehindu.com/ccidist-ws/th/…

Hearing loss affects 1-2 in every 1000 newborns, often due to genetic defects in numerous genes. Gene therapy may hold promise for these children offering hope for their auditory future. Vinod Scaria and I discuss this in The Hindu Read the full article: epaper.thehindu.com/ccidist-ws/th/…