Our latest #research on a rare muscular dystrophy cases from South India (Dr A Nalini, NIMHANS) published in SpringerNature@Neurogenetics Journal. #CSIR-IGIB rdcu.be/cqZ8M link.springer.com/article/10.100…

Accurate and simple FXN-GAA repeats (Friedreich ataxia loci) estimation by long read targeted sequencing. biorxiv.org/content/10.110…

Accurate and simple FXN-GAA repeats (Friedreich ataxia loci) estimation by long read targeted sequencing. Oxford Nanopore Oxford nanopore biorxiv.org/content/10.110…

Accurate and simple FXN-GAA repeats (Friedreich ataxia loci) estimation by long read targeted sequencing. Oxford Nanopore biorxiv.org/content/10.110…

Accurate and simple FXN-GAA repeats (Friedreich ataxia loci) estimation by long read targeted sequencing. biorxiv.org/content/10.110… Every bit of lyf spent to make lives better #stopwar#WHO#NIH#scientists #worlddoctors #humanity War pandemic # save lives. Why lockdown/mask/vaxin

'I don't think there is a safe place': Kyiv residents fearful as Russian invaders close in nbcnews.com/news/world/liv… via NBC News Aren't any better things for the world to offer than just saying good luck :( #UN

Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool onlinelibrary.wiley.com/doi/full/10.10… The experience of 10 years of common genetic ataxia subtypes for ≈5600 patients’ referrals (Pan-India) received at a single center is shared herein.#IGIB

This story is special to me. Took me a long time to write. It is not just about a rare disease, but much more— relationships, love & fear. “Who din hawa hue jab paseena gulab tha. Ab itra bhi lagao toh mohabbat ki boo nahin.” Appreciation 🧵 (1) fiftytwo.in/story/off-bala…

Sometime back, Ankur Paliwal visited a home in which 3 single beds were arranged in the shape of an inverted ‘U’. Mohammad Hamid lay on the bed at the back. His wife lay to his right. Her eyes were fixed on the third bed, occupied by their son. Their story: fiftytwo.in/story/off-bala…

AddThis | Home doi.org/10.1016/j.scr.…

A rare resource for probing KIF5A function towards converging cross talks between different neurodegenrative disorders.#KIF5A#ALS#Ataxia doi.org/10.1016/j.scr.…

AddThis | Home doi.org/10.1016/j.scr.… CSIR-IGIB

Sequencing Trinucleotide GAA repeats of FXN (Friedreich ataxia), Yup upto 1000 and above using Nanopore in a cost effective way!! to Go.. academic.oup.com/braincomms/art…

New breakthrough in the fight against Friedreich’s ataxia vigyanprasar.gov.in/isw/New-breakt… #sciencetechnologynews via India Science Wire

Eid mubarak!!! عيد مبارك

Computational and experimental hunt for expansion prone tandem CNG repeats in human genomes biorxiv.org/content/10.110…

Genetic Investigation camp at hyderabad on 06/08/2023, supported by GOMED - CSIR IGIB

STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genome academic.oup.com/database/artic… CSIR-IGIB way forward for mapping Unsolved rare disorders and missing inheritance....!! new from our Lab.

Marking the completion of 10,000 genomes from 83 Indian ethnic populations, GenomeIndia project featured in Nature Genetics GenomeIndia was launched in 2020 as a consortia of 20 institutes converging their expertise to undertake this task... read more nature.com/articles/s4158…