I taught (and co-taught) a course on human population genetics from 2000-2024. Having retired, I'm now making all the course materials public: github.com/alanrogers/p... #popgen #evbio
27.11.2025 19:10 β π 256 π 92 π¬ 4 π 0@benjaminhgood.bsky.social
Assistant Professor of Applied Physics @Stanford. Theoretical biophysics, evolutionary dynamics & microbial evolution. https://bgoodlab.github.io/
I taught (and co-taught) a course on human population genetics from 2000-2024. Having retired, I'm now making all the course materials public: github.com/alanrogers/p... #popgen #evbio
27.11.2025 19:10 β π 256 π 92 π¬ 4 π 0Hot off the press! Our latest paper led by @fernpizza.bsky.social, understanding how plasmids evolve inside cells. These small, self-replicating DNA circles live inside bacteria and carry antibiotic resistance genes, but also compete with one another to replicate. 1/
www.science.org/doi/10.1126/...
Our latest paper is out with @adiop.bsky.social and @gmdouglas.bsky.social. We analyzed the extent of homologous recombination between bacterial species (introgression) and how it affects species borders (it can vary a lot depending on the approach used to classify species!). rdcu.be/eQAMf
18.11.2025 21:00 β π 60 π 44 π¬ 1 π 0Schematic diagram showing microbial strains migrating between mouse gut microbiomes.
(while the underlying biology is very different, there are some striking parallels to the migration of bacterial strains across different local gut microbiomes)
18.11.2025 15:39 β π 1 π 0 π¬ 0 π 0We think these intermediate levels of migration could be very interesting, by preserving the large-scale spatial structure of GCs, while still allowing positively selected lineages to expand across a wider range of GCs than would otherwise be possible - potentially balancing diversity & selection.
18.11.2025 15:24 β π 1 π 0 π¬ 1 π 0Schematic diagram illustrating spatial migration of B cells during affinity maturation.
We show that these local migrations follow a clock-like process @ a rate of βΌ1/50 cell divisions - roughly uniform across lineages & time. Plus, migrant B cells continue to evolve w/in their new germinal centers at similar rates, such that the largest lineages in each GC often originate from another
18.11.2025 15:24 β π 0 π 0 π¬ 1 π 0& last but not least, a new preprint led by PhD student John McEnany (w/ Ivana Cjivovic) looking @ the evolutionary dynamics within our immune system. Using spatial transcriptomics data from the tonsil, we identify a surprisingly large role for local migration of B cells during affinity maturation.
18.11.2025 15:24 β π 3 π 0 π¬ 1 π 0π’ Our Dept. of Systems Biology at Columbia University has an open tenure-track Assistant Professor position in the broad area of quantitative biology. Come join our awesome department in NYC! Please circulate.
apply.interfolio.com/177622
Suggested deadline: 12/15/2025.
@columbiasysbio.bsky.social
Understanding this effect really changed how I think about the fates of new mutations in the presence of clonal interference β and leads to a mathematical formalism that I hope will be useful in other contexts as well.
17.11.2025 14:14 β π 0 π 0 π¬ 0 π 0In this regime, invading ecotypes effectively "mortgage" their ecological advantage to increase their initial growth rate. But they eventually pay a price at higher freqs, when their ecological advantage suddenly dissipates. This echoes recent findings by P. Barrat-Charlaix & @neher.io in SI models.
17.11.2025 14:14 β π 0 π 0 π¬ 1 π 0Schematic showing how a rapidly evolving population clusters into a smaller number of distinct ecotypes, comprising individuals with similar resource uptake strategies but different genotypes & overall fitness.
We show that despite this large mutational influx, rapidly evolving pop'ns naturally cluster into a smaller # of distinct βecotypesβ, even when their genetic diversity is much larger. This non-eq analogue of competitive exclusion is driven by a dynamical priority effect that favors resident strains.
17.11.2025 14:14 β π 4 π 2 π¬ 1 π 0Schematic diagram showing an evolving ecosystem at high and low mutation rates.
Most existing models of evolving ecosystems assume that evolution occurs very slowly, so that the ecosystem can always equilibrate before the next mutation appears. Here we focus on the more empirically relevant case where ecology & evolution act on similar timescales, as often occurs for microbes.
17.11.2025 14:14 β π 0 π 0 π¬ 1 π 0Another new preprint from former PhD student Daniel Wong (now @ ENS) has been a long time in the making, and builds on our recent efforts to model eco-evolutionary feedbacks in rapidly evolving microbial populations that compete for different resources (1/n)
17.11.2025 14:14 β π 9 π 2 π¬ 1 π 0π£ New preprint from us at phagefoundry.org π£
A solid machine learning framework & to predict strain-level phage-host interactions across diverse bacterial genera from genome sequences alone. Avery Noonan from the Arkin Lab led this massive effort
www.biorxiv.org/content/10.1...
Their adaptive reversion model may provide part of the answer, but strong assumptions still needed to account for long-term optimization of ~90% of all protein coding sites. For me, this remains one of the more interesting puzzles of microbial pop gen, since it's such a common trend across species.
16.11.2025 15:26 β π 2 π 0 π¬ 0 π 0How natural selection manages to optimize such weak fitness costs in the face of all the adaptation & genetic hitchhiking we think is happening on shorter evolutionary timescales is still a major puzzle. Previous work by Paul Torrillo & @contaminatedsci.bsky.social suggests that it's not so easy!
16.11.2025 15:26 β π 5 π 0 π¬ 1 π 0Clonal dN/dS dynamics in human gut bacteria after correcting for recombination.
We use this finding to re-examine models of purifying selection & adaptive reversion in human gut bacteria. After correcting for HGT, we show that most protein-coding variants are eliminated ~10x more slowly than previously assumed. Yet they are still reliably purged on 10-100k yr timescales.
16.11.2025 15:26 β π 4 π 0 π¬ 1 π 0Schematic showing how homologous recombination can influence dN/dS between conspecific strains of bacteria.
Many studies have found that w/in-species dN/dS decays w/ the genetic distance between strains, which is often attributed to natural selection. Here Zhiru shows that a large portion of this trend can be quantitatively explained by the accumulation of horizontally transferred DNA segments over time.
16.11.2025 15:26 β π 9 π 3 π¬ 1 π 0The first is from former PhD student Zhiru Liu @zzzhiru.bsky.social (now in @bengrbm.bsky.social's group @ MSK) examining the long-term patterns of selective constraint β measured by the classical ratio of nonsynonymous to synonymous mutations (dN/dS) β within recombining populations of bacteria.
16.11.2025 15:26 β π 16 π 9 π¬ 2 π 0It's been a busy few months for our group so wanted to highlight a few other recent preprints weβve posted that I havenβt had the chance to share yet... (1/n)
16.11.2025 15:26 β π 17 π 8 π¬ 1 π 2Very happy to share our recent work @cultivarium.bsky.social on genetic tools for Ideonella sakaiensis, a (Betaproteo-)bacterium that degrades PET plastic.
We identified a plasmid vector for the strain and generated a large RB-TnSeq library, screening for genes impacting plastic degradation.
Amazing journal cover for the new Trends In Microbiology special issue on geographic diversity in microbiology
www.cell.com/trends/micro...
Kudos to our superstar grad student @sophiejwalton.bsky.social! One of the most interesting and surprising (at least to me) studies I have been involved in. Very curious to know what people think of it! @benjaminhgood.bsky.social
11.11.2025 17:37 β π 9 π 3 π¬ 0 π 0Excited to share some new work led by grad student Sophie Walton (w/ @petrovadmitri.bsky.social). We used in vitro gut communities to study how natural selection acts on strains of the same species as they compete within larger communities. Check out Sophie's thread below for details!
12.11.2025 03:43 β π 28 π 13 π¬ 0 π 1π¨ Microbiologists! We are recruiting Assistant / Associate Professors in 3 collaborative areas of our U. Pittsburgh School of Medicine.
1) MMG (my dept): fundamental research in med micro
2) Peds ID / I4Kids institute
3) Center for Vaccine Research
π to all 3 w/info: www.linkedin.com/posts/vaughn...
Now hiring a computational postdoc (evolutionary genomics, molecular evolution) in my lab at Emory University.
If youβre interested in population genetics, fitness landscapes, and viral evolution β get in touch.
faculty-emory.icims.com/jobs/151181/...
The constant barrage of terrible news on bluesky has made me feel weird about promoting papers, but people in the lab have been doing so much amazing work over the past few months that I want to share a few brief teasers/links:
10.09.2025 16:46 β π 66 π 22 π¬ 2 π 1How common are frequency dependent fitness effects?
New preprint out today π
doi.org/10.1101/2025...
Drifting into speculation: I think these data support the picture that gut microbes can spread much faster than human genes. Strong geographic barriers can be still be very important (as in the Tsimane & Hadza case) but the magnitude of this effect
stands out compared to other contemporary pop'ns.
A figure panel depicting the amount of recent strain sharing of Ruminococcus bromii strains between different human populations.
Interestingly, of the subset of species shared w/ industrialized pop'ns, some show evidence of recent transmission, while others suggest a more ancient association. Among these, the genetic isolation between Tsimane & Hadza strains was generally larger than between comparable industrialized pop'ns
17.08.2025 21:59 β π 2 π 0 π¬ 1 π 0