Prajna Hebbar

@prajnahebbar.bsky.social

PhD Candidate, Computational Genomics Lab UC Santa Cruz.

New issue alert👉https://cell.com/cell/current On the cover: The Telomere-to-Telomere Consortium has finished the complete, diploid genome of a person. The cover is inspired by a karyotype of the chromosomes in metaphase, representing the two haplotypes as different colors.

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There are a horrifying number of computer science professors that still just "solve problems" with no thoughts. People who publish papers like: "We made an algorithm that can detect human shapes from infrared data, and even works with children behind tent covers."

I've been documenting a pair of black-capped chickadees nesting in our garden as they fly back & forth every few minutes, hunting meals. An avg clutch of 6 to 8 chickadees requires 3,000 to 5,000 feedings over the ~16 days from hatching to fledging. Most popular foods: caterpillars, moths, spiders.

A collage of 16 photos of black-capped chickadees. Each photo depicts a closeup of a single chickadee with prey in their mouth, such as a caterpillar, adult moth, other winged insect, or spider. The chickadees are small songbirds with gray-white plumage and patches of black on their heads and throats.

I’ve officially resigned as Associate Editor for Frontiers in Systems Neuroscience. It used to be a reputable journal, but became a case study in how forced automation destroys academic integrity. 👇

Happy to highlight new findings by Vanesa Getseva and Lin Poyraz about the sources of variation in germline mutation rates among humans: www.biorxiv.org/content/10.6... Joint work with Anastasia Stolyarova and @ipsitaagarwal.bsky.social. 1/n

A sibling study of variation in parental mutation rates

People are born with variable numbers of de novo germline mutations (DNMs), depending primarily on the ages of their parents. To explore additional causes, we developed an approach to call DNMs from nucleotide differences between siblings in genomic regions inherited identical by descent from both parents. Applying it to whole genome sequences from 28,985 sibling pairs of diverse genetic ancestries present in the UK Biobank and All of Us datasets, as well as 2,330 trios, we identified >800K autosomal DNMs and characterized mutation phenotypes in 27,645 sets of parents. We found subtle shifts in the mutation spectrum but no differences in total DNM rates among genetic ancestry groups, or between smokers and non-smokers. Testing for associations between parental mutation phenotypes and their burden of loss-of-function and deleterious missense variants in a set of 180 DNA repair and maintenance genes, we discovered that disruptions in REV1 and LIG1 increase germline mutation rates, and thus that rare mutator alleles segregate in population cohorts. ### Competing Interest Statement The authors have declared no competing interest. NIH, R35 GM083098

biorxiv.org

We built the first complete genome for the common marmoset, fully resolving regions that were previously missing: centromeres, acrocentric short arms, and more. A new reference genome for anyone working with marmosets. This was an awesome collaborative effort & I’m grateful to all my co-authors! 🧬

bioRxiv Genomics@biorxiv-genomic.bsky.social · 5mo ago

A Complete Genome for the Common Marmoset https://www.biorxiv.org/content/10.64898/2026.03.25.713844v1