Awesome work by @mdbakhtiari in Vineet Bafna's group to rapidly and accurately genotype variable number tandem repeats (VNTRs). Enables the discovery of eQTL elements based on those previously difficult to quantify VNTR expansion loci.
When a cancer genome carries focally amplified oncogenes, what genomic structures permit them? Can we reconstruct the amplified rearrangements, like #ecDNA and #BFB?
Oftentimes yes, we can! Out today in @NatureComms is our paper on AmpliconReconstructor. https://t.co/cvvpEwMso0
Our @biorxivpreprint on VNTRs impact on gene expression regulation in GTEx is out now! We show VNTRs are likely eQTL causal variants in many cases. Thanks to @mgymrek@bvhalldorsson@KariStefans Vineet Bafna and many others!
https://t.co/dBjlDm1NA9
Check out our paper about assembling centromeres from long error-prone reads! We present the first automated assembly of human centromere X.
https://t.co/t3yCB225rs
Check out our lab's @biorxivpreprint: A reference haplotype panel for genome-wide imputation of short tandem repeats https://t.co/tQ1LmUr0Gc awesome work by @shubsaini and @ileena_mitra #genomics#bioinformatics
iSAFE (integrated Selection of Allele Favored by Evolution) for identifying the target mutation in a selective sweep, Akbari et al. w/ Vineet Bafna of @UCSanDiego@UCSDJacobs
Compare & contrast with SWIF(r) coming soon to a tweet near you.
@naturemethods
https://t.co/fsxlOc6CcQ