kavita pandhare

Happy to share BRCAIndica, our endeavour in making ACMG-AMP pathogenicity classifications available for over 10,000 BRCA1/2 variants. @vinodscaria @anu_iris @kavitapandhare link.springer.com/article/10.100…

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. @vinodscaria and I discuss this in @the_hindu Read the full article: epaper.thehindu.com/ccidist-ws/th/…

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. @RcBHOYAR and I write in @the_hindu Read the full text here epaper.thehindu.com/ccidist-ws/th/…

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 @karkinoshealth

Glad to contribute towards establishment of the country's first state-of-art Next-generation sequencing laboratory at @MoHmv Maldives. Thanks to WHO Maldives and MoHmv Maldives WHO India and a super energetic Maldives Team @WHOSEARO with @SridharSivasub3 @vinodscaria @bani_jolly

🆕Here is a First Report on Current #lumpyskindisease Outbreak, In India. Genetic and Phylogenetic analysis of the LSD Viral Isolate from the Current LSD Outbreak in India Suggest a Distinct Lineage of the Virus. @vinodscaria @bani_jolly @SridharSivasub3 👇biorxiv.org/content/10.110…

Announcing the #IndiGen HLA Allele frequency resource enabling researchers, clinicians and immunologists. The resource provides frequencies of high, medium and low resolution HLA allele frequencies in India clingen.igib.res.in/HLA/

"Alone we are Rare together we are Strong" on this Rare Disease Day I stand with Rare. #ICareforRare #WeAreCSIR #RareDisease #RareDiseaseDay #Genomics #GUaRDIAN

Pleased to share the BGvar resource publication, now online in Transfusion Medicine. BGvar is a comprehensive repository of human blood group alleles and antigens built in collaboration with @QUT. Read more at doi.org/10.1111/tme.12…

The ESC resource publication is now online in @NAR_Open . ESC is one of the most comprehensive collections of evidence on SARS-CoV-2 immune escape variants. Read more at academic.oup.com/nar/advance-ar…

The motivation has been the concept of #Genomic #Beacon framework Federated discovery and sharing of genomic data ncbi.nlm.nih.gov/labs/pmc/artic… The web interface allows one to slice the data by Lineage, by State, Date-line as well as specific mutations. The #OpenAPI will come soon.

Introducing the COVID-19 Beacon Query Browser which enables search across the #COVID19 #genome sequences from #India clingen.igib.res.in/covid19genomes/ Credits: @kavitapandhare @bani_jolly

COVID-19 Genome Surveillance Dashboard is now online integrating data from #INSACOG as well as the State Genomic Initiatives of #Kerala and #Maharashtra clingen.igib.res.in/covid19genomes/ Credits: @kavitapandhare @bani_jolly and NGS & analysis team at @IGIBSocial

Explainer on L452R+E484Q : The L452 and E484 residues in the spike protein map to the receptor binding domain (teal) and overlap with residues associated with immune (antibody) escape More evidence on these mutations can also be found on the ESC database clingen.igib.res.in/esc

Check out our online resource ESC, comprising #SARSCoV2 #ImmuneEscape variants and their annotations at clingen.igib.res.in/esc/ Preprint available at biorxiv.org/content/10.110… #CSIRfightsCOVID @vinodscaria @kavitapandhare @AfraShamnath @mohamedimran_s @bani_jolly @IGIBSocial

Announcing ESC - a comprehensive resource for SARS-CoV-2 immune escape variants and their annotations. biorxiv.org/content/10.110… #CSIRfightsCOVID #ImmuneEscape #SARSCoV2 #VOC #N440K #E484K

#FAVICOV, a resource for detailed annotation of over 400 #functionally relevant #genetic variants in #SARSCoV2 from literature. Access the online resource at clingen.igib.res.in/favicov/ @vinodscaria @kavitapandhare @AfraShamnath @bani_jolly @MokshadaSethi @IGIBSocial @CSIR_IND

Check out the comprehensive compilation of #SARSCOV2 immune #escape variants at clingen.igib.res.in/esc/ #CSIRfightsCOVID19 @kavitapandhare @AfraShamnath @mohamedimran_s @bani_jolly @vinodscaria @IGIBSocial @CSIR_IND

Announcing #FAVICOV a unique resource for functionally relevant variants in #SARSCoV2 . Indexing over 430 unique variants from literature. Access at clingen.igib.res.in/favicov/ #CSIRfightsCOVID19

The completion of sequencing 1029 individuals in just 6 months is a miracle that was brought to reality by @vinodscaria @SridharSivasub3 and the wonderful team. #IndiGenomes encompasses 55,898,122 genetic variants from distinct states. academic.oup.com/nar/advance-ar…