Rhett Rautsaw

@reptilerhett.bsky.social

All views are my own Field Applications Bioinformatic Support (FABS) Scientist @pacbio.bsky.social PostDoc: Tasmanian Devils @wsupullman.bsky.social & @usouthflorida.bsky.social PhD: 🐍 venom evolution @SnakeLabClemson

Congratulations to Sampled on its new five-year VA contract supporting the Million Veteran Program! 👏 With multiple PacBio Revio systems, Sampled is bringing scalable HiFi sequencing to one of the world’s largest research programs of its kind. Read more: https://prn.to/4y5klHq

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Benchmarking by Harvey et al. shows PacBio HiFi achieves higher indel & SV recall at 20x than ONT achieves at 60x+. 📊 Citing the right peer-reviewed data is key to a winning grant proposal. See how our literature library helps you write yours faster: https://bit.ly/4ycWZ3q

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Leveling the playing field, one long read at a time. Vega SPRQ-Nx chemistry is now shipping! Bring higher throughput, lower DNA input, shorter run times, and expanded methylation detection to your benchtop. What will you discover? Learn more: bit.ly/3TCbMoR

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T2T genomics is quickly becoming less of an endpoint and more of a starting point for discovery. A new Cell issue features 13 papers on complete diploid genome assemblies across species like humans, marmosets, horses, giraffes, and more. Explore the research: bit.ly/4wAdZiw

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Big updates coming to Vega! SPRQ-Nx chemistry drops cost per Gb by 40% with 90 Gb yield, $995 run pricing, 500 ng input minimums, 2-to-4 hour run times, and 21 CFR Part 11 compliance controls. Read the full press release to explore the full specs: bit.ly/3Rxyjmd

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Though I will not make it to #Botany2026, Doug Soltis and Jacob Landis will tag-team my talk on Monday at 2:15 pm in Population Genomics (San Ignacio)!

Evolutionary Trajectories of a Co-Occurring Mixed Cytotype Autopolyploid System, Galax urceolata  by Michelle L. Gaynor, Jacob B. Landis, Douglas E. Soltis, Stephen A. Smith, and Pamela S. Soltis
Shelly Gaynor@shellygaynor.bsky.social · 3mo ago

I was really excited to attend #Botany2026, but sadly my cat is very sick and I decided I couldn't leave her right now. I believe @jlandisbotany.bsky.social will be giving my talk. And luckily the @soltislab.bsky.social can do the workshop without me. Really sad to miss this year!

Registration is still open for our webinar on how SPRQ-Nx chemistry on Vega drives benchtop long-read sequencing performance up and costs down. Learn how lower DNA input, higher HiFi yield, and 21 CFR Part 11 support accelerate biopharma, microbiology, and more. Register: bit.ly/3RjPzLo

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The new Rapid HiFi WGS Resource Bundle is now available to accelerate your time-critical genomic research. Get instant access to four essential pieces: our latest technical note, ESHG poster, application note, and blog article. Access the resources now: bit.ly/4eYvYIp #PacBio

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Registration is open for our webinar on how SPRQ-Nx chemistry on Vega drives benchtop long-read sequencing performance up and costs down. Learn how lower DNA input, higher HiFi yield, and 21 CFR Part 11 support accelerate biopharma, microbiology, and more. Register here: bit.ly/3RjPzLo

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Huge congratulations to the All of Us Research Program on their historic data release! 🌍🧬 Thrilled to see HiFi sequencing contribute through 14K+ long read genomes. Through their participation, 747K+ individuals are making this possible. Details: bit.ly/4gOgSYr

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A new Nature Genetics piece from @radboudumc.bsky.social outlines Near-Perfect Genome Sequencing (NPGS): a framework combining long-reads, diploid assembly, pangenomes, and AI to shift from fragmented testing to a single comprehensive genomic assay. Read more here: go.nature.com/4ey5YF0 #PacBio

Near-perfect genome sequencing in medical genetics - Nature Genetics

This Perspective introduces near-perfect genome sequencing, which encompasses diploid genome assembly, pangenome references and artificial intelligence-driven variant interpretation, and proposes a ro...

go.nature.com

The FDA's new draft guidance on genome editing safety highlights why detecting large indels and chromosomal abnormalities is critical, where short-reads fall short. HiFi sequencing offers >99.9% accuracy to characterize all editing outcomes. Learn more: bit.ly/49ZpV4S

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Excited to share that I will be joining Florida State University as an Assistant Professor starting in January 2027! I’m thrilled to build my lab at FSU in the Ecology & Evolution Division within the Department of Biological Science — stay tuned! A huge thank you to my village for all the support!

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How do you navigate the traditional trade-offs in sequencing? Today, you can capture genetic variation and native methylation simultaneously in a single run without extra prep. Check out our blog to see how HiFi sequencing has rewritten the old rules: bit.ly/3RijsLN #PacBio

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If your Nanopore- based long-read data is full of noise, is it actually useful? Next in our Top 5: Why choose #PacBio HiFi over other long-read methods? The answer is 99.9% accuracy. No GC bias, no repetitive region dropouts, and reliable results for every species. Watch: bit.ly/4cBxnVp