New manuscript about BCFtools/liftover, a tool that converts genetic variants between reference genome assemblies with better support for indels and multi-allelic variants: https://t.co/NGgzm52KfJ 1/8
@kauralasoo@doctorveera The code exists, but you don't currently have permission to access it. It will be made available soon, once the repository is made public. Stay tuned! This is in accordance with company policies.
We have in town a new genotype imputation software Selphi that "significantly outperforms Beagle5.4, Minimac4 and IMPUTE5 across various metrics (...) and allele frequencies (...)"
And it comes from a commercial Bioinformatics company Omicsedge
https://t.co/KLYubka2Q5
Happy #DNADay! 🧬
#NationalDNADay is a day when you can learn more about genetics, celebrate the advances in research, and explore how it can impact their lives!
https://t.co/3FjmzF1V8K