Laurence Ettwiller
@ettwiller.bsky.social
110 followers 72 following 29 posts
Scientist working at New England Biolabs. Tweets and comments represent my personal opinion and do not necessarily reflect the opinions of New England Biolabs.
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ettwiller.bsky.social
Dream of avoiding carryover contamination in your NGS experiment?
Check out our latest preprint:
🧬 “A Novel NGS-Compatible Enzymatic Strategy Enables Carryover Contamination Removal and Enhances Sequencing Performance” www.biorxiv.org/content/10.1...
Reposted by Laurence Ettwiller
🧪⚒️Just released an episode on the dynamics of subduction zones with Claudio Faccenna. Not only do trenches roll back and move laterally, they also advance and flip polarity. But when they penetrate the viscous lower mantle they get locked in place. Enjoy listening!
The figure shows sections of P-wave tomography anomalies along the yellow lines on the map (Fukao & Obayashi, 2013), seismicity (orange dots on profiles; Engdahl et al., 1998), plate velocities (orange vectors; Argus et al., 2011), and volcanoes (cyan inverted triangles; Siebert & Simkin, 2023).  The Western Pacific and Japan subduction zones (the two most northerly zones) do not appear to penetrate the lower mantle, unlike those of Indonesia and Kermadec (north of New Zealand).  Whether a slab penetrates the lower mantle depends on factors such as the duration of subduction and the angle at which the slab reaches the 660-km discontinuity, with steeper angles favoring descent.

Becker, T and Faccenna, C. (2025), Tectonic Geodynamics, Princeton University Press Subduction zones along the west coast of the Americas.  In the podcast, Faccenna described how the slab subducting below the Andes has entered the lower mantle where its lateral movement is restricted by the higher viscosity there.  The subduction zones beneath northern South America and Central America show evidence of penetration into the lower mantle, reaching depths of 1,300 km or more.  By contrast, the younger Caribbean subduction zone does not. 

Becker, T and Faccenna, C. (2025), Tectonic Geodynamics, Princeton University Press Left: map showing seafloor ages in the western Pacific.  The back-arc basins shown appear mainly as the red and orange regions, i.e., having the youngest ages of 0 and 30 million years.  Center: more detailed seafloor age map of the Izu-Bonin-Marianas region.  Right: P-wave tomography sections along the green lines labeled A, B, and C, revealing the varying shape of the subduction zone going from north to south.

The western Pacific subduction zone is characterized by back-arc extension in the overriding plate that began within the last 30 million years (left panel).  Tomography and seismicity data show that along the Izu–Bonin region (section B1–B2), a double subduction system is present, resulting from subduction of both the Pacific Plate (to the east) and the Philippine Plate (to the west).

Becker, T and Faccenna, C. (2025), Tectonic Geodynamics, Princeton University Press The Izu–Mariana subduction system is unique in that the trench is advancing toward the overriding plate (right panel).  Bottom left: tomographic section along the red line on the map at right shows the two subducting slabs.  Top left: numerical model of single subduction and double subduction.  The double subduction simulation replicates quite a few features appearing on the tomographic section, such as the apparent flattening out of the subducting slabs between the depths of 400 and 600 km.  In a single-slab system, the trench migrates backward, whereas in a double-slab system, the rear slab drives trench advance.  The simulation also reproduces the tomographic section (bottom left, section along the red line on the map at right), which clearly shows the presence of two subducting slabs.

Faccenna, C. et al. (2018), Tectonophysics, 746, 229
Reposted by Laurence Ettwiller
biorxiv-genomic.bsky.social
A novel NGS-compatible Enzymatic Strategy Enables Carryover Contamination Removal and Enhances Sequencing Performance. https://www.biorxiv.org/content/10.1101/2025.08.01.668201v1
ettwiller.bsky.social
Read the full story & explore the data here:
www.biorxiv.org/content/10.1...

👏 This is an amazing work from Amanda DeLiberto at #NEB @nebiolabs.bsky.social

#NGS #genomics #molecularbiology #preprint #contamination #sequencing
ettwiller.bsky.social
This dual-function strategy is ideal for:
🔹 Clinical & diagnostic sequencing
🔹 Low-input or precious samples
🔹 Metagenomics
🔹 Any workflow where contamination is a problem
ettwiller.bsky.social
Implementation is simple:
➕ Add Fpg & 7-deaza-dGTP directly to your PCR mix
⏱️ Brief pre-amplification incubation
No added steps, no workflow disruption
ettwiller.bsky.social
Why is this different?
7-deaza-dGTP is accepted by high-fidelity polymerases (unlike dUTP)
Fpg cleaves 7-deaza-dG-containing contaminants
Bonus: 7-deaza-dGTP reduces GC bias and improves sequencing coverage!
ettwiller.bsky.social
Our method changes that.
We introduce a new strategy using:
✅ 7-deaza-dGTP
✅ Fpg glycosylase
Together, they provide similar carryover contamination removal as dUTP/UDG and work seamlessly in standard NGS pipelines.
ettwiller.bsky.social
Contamination between NGS runs can compromise sensitive applications—from clinical diagnostics to ancient DNA.
Until now, enzymatic solutions like dUTP/UDG had one major flaw: they're are not compatible with high-fidelity NGS workflows.
ettwiller.bsky.social
Dream of avoiding carryover contamination in your NGS experiment?
Check out our latest preprint:
🧬 “A Novel NGS-Compatible Enzymatic Strategy Enables Carryover Contamination Removal and Enhances Sequencing Performance” www.biorxiv.org/content/10.1...
ettwiller.bsky.social
(Sorry for the late reply - I was hiking the Alpine section of the GR5 trail over the past six days)
ettwiller.bsky.social
Phages containing dU can be sequenced using polymerases that tolerate dU, such as Taq or Q5U. But thermostable polymerases are not strictly required, as only the first round of amplification needs to successfully copy the dU-containing templates to allow their propagation in downstream PCR cycles.
ettwiller.bsky.social
dU containing phages have been described (for ex : PMID: 34033748, PMID: 35934259) while Mikael Skurnik's lab isolated YerA41, a Yersinia ruckeri Bacteriophage that cannot be sequenced due to bulky modifications (PMID: 32517038).
ettwiller.bsky.social
And yes- standard high-throughput sequencing misses bulky DNA modifications and those recognized as damage, like deoxyuridine (dU), because most standard protocols use high-fidelity polymerases that typically contain a dU pocket and stall at dU.
ettwiller.bsky.social
This estimate comes from metaGPA for which high-throughput sequencing of DNA resistant to cytosine deamination is compared to total viral metagenomic DNA. Of course, only DNA that can be amplified (e.g., with Q5 polymerase) is detectable.
ettwiller.bsky.social
We estimate that 2–3% of contigs from viral metagenomes originate from genomes in which all canonical cytosines (C) have been replaced by modified bases (elifesciences.org/articles/70021). And that’s just for cytosine. (data from sewage and coastal metagenomes)
Reposted by Laurence Ettwiller
erictopol.bsky.social
This is wild!
Engineering E. coli bacteria to turn plastic waste into paracetamol (Tylenol)
www.nature.com/articles/s41...
www.nature.com/articles/s41...
Reposted by Laurence Ettwiller
dijiang319.bsky.social
🧬🧫🦠 @science.org Bacterial reverse transcriptase synthesizes long poly-A–rich cDNA for antiphage defense | Science www.science.org/doi/10.1126/... #microbiology #bacteriophage #antiphage #immunity #DNA #RNAsky #RT #Cryo-EM #DRT9
Reposted by Laurence Ettwiller
plosbiology.org
The BASEL collection of E. coli #phages is limited by its host strain. @humollidorentina.bsky.social @damienpiel.bsky.social @aharms485.bsky.social &co use a modified host to add 36 new phages, revealing roles of O-antigen in recognition & R-M systems in immunity @plosbiology.org 🧪 plos.io/4jirGvX
A fanciful depiction of BASEL phages on a roadmap. Credit: Fabienne Estermann
ettwiller.bsky.social
A big shoutout to the team behind Proxi-RIMS-seq2: Weiwei Yang and Yvette Luyten from @NEBbiolabs (from my lab and Rich Roberts' lab), along with the team at @phasegenomics. Special thanks to REBASE for hosting the data.
ettwiller.bsky.social
Proxi-RIMS-seq2 applied to native microbiomes uncovers hundreds of known and novel m5C methyltransferase specificities. A collaboration between @NEBbiolabs and @phasegenomics
ettwiller.bsky.social
Proxi-RIMS-seq now enables direct study of epigenetic modifications in microbiomes using Illumina sequencing on genome-resolved microbiomes ! Learn more in our latest work with @phasegenomics:
doi.org/10.1093/nar/...
pendingpublications
Pending Publication
doi.org
Reposted by Laurence Ettwiller
Reposted by Laurence Ettwiller
saimihanma.bsky.social
Hair ice!! This is caused by a fungus in the wood. I'm always excited to find it when it gets cold.
A twig with ice growing out like hair in delicate strands