Adarsh Prasannakumar
@adarshpp
Genomic Medicine, Human Genetics and Bioinformatics | LIFE ✨
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#Amrita Vishwa Vidyapeetham has once again emerged as the 7th best #university in the #NIRF Rankings 2024 by Government of #India announced today by Hon. @EduMinOfIndia Shri @dpradhanbjp. We express our heartfelt gratitude to our dear students, parents, faculty, alumni, & all.
MAHE has secured the 4th position in the National Institutional Ranking Framework (NIRF) 2024 in the University category, marking an impressive leap of two places from last year. Kudos to everyone who contributed to this success! #MAHE #NIRF2024 #TopUniversity #mahemanipal
Updated my metro list! Chennai Metro takes the 5th spot, joining Kochi, Hyderabad, Delhi, and Bangalore Metro! Which city will be next? #MetroList #ChennaiMetro #UrbanTransport @ChennaiMetRail
Everyday is a new adventure, where you face and welcome new challenges as guests, who are uninvited!
Proud to have concluded my tenure at Kasturba Medical College's Dept. of Medical Genetics. Deeply grateful for the growth in bioinformatics, genomics, & human genetics. Thank you, colleagues, for the invaluable support! @kmc_manipal @GeneticsManipal
We are committed to the cause of families with rare genetic disorders @GeneticsManipal @kmc_manipal @BhatVivekananda @pe_radhakrishna @PUpadhyai @ShaliniSNayak1 @MAHE_Manipal
The 10,000 Genome Project led by CCMB, @IGIBSocial, @FollowDbtNibmg and @CBR_IISc with 16 other institutes is now completed! This is a key milestone towards finding Indian population specific genetic variants & working towards more effective healthcare. thehindu.com/sci-tech/scien…
Humiliating experiences can be a powerful reminder of why #RespectGoesBothWays. Treat everyone with dignity, from colleagues to interviewees. Remember, kindness is strength. #EveryInteractionMatters
"Bioinformatic analysis and interpretation is the core step in NGS-based diagnostics of rare disease" A good insight into the bioinformatics part of rare disease studies. doi.org/10.1093%2Fbib%…
academic.oup.com
Bioinformatics of germline variant discovery for rare disease diagnostics: current approaches and...
Abstract. Next-generation sequencing (NGS) has revolutionized the field of rare disease diagnostics. Whole exome and whole genome sequencing are now routin
A great achievement indeed and I am privileged to be a part of it. Congratulations to the entire team 🎉
Thrilled to share that our paper, "Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications," is now officially published in Clinical Genetics after four years of dedicated work! onlinelibrary.wiley.com/doi/full/10.11…
▶️ What can our ancestors'genomes tell us about modern health ? @sridharsivasubb and I write in @the_hindu
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