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Seppe De Winter

@seppedewinter.bsky.social
86 followers 111 following 18 posts

Post-doctoral researcher at aertslab VIB-AI KU Leuven. seppedewinter.net

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Reposted by Seppe De Winter
Alexandra P @alexanrna.bsky.social · 16/04/2026
1/ 🧬 Happy to share our new preprint on modeling cis-regulatory variation in human brain enhancers across a large Parkinson’s disease cohort: www.biorxiv.org/content/10.6... Details in the thread below:
biorxiv.org
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Seppe De Winter @seppedewinter.bsky.social · 08/04/2026
Check out our @natmethods.nature.com publication on CREsted, a user-friendly sequence-to-function framework to decipher enhancer codes and design synthetic enhancers! 🦎
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Reposted by Seppe De Winter
Hannah Dickmänken @hannahdckmnkn.bsky.social · 29/01/2026
Paper alert! 💻 How many cells do you need to train reliable deep learning models in regulatory genomics? We asked how data quality, sequencing depth, and dataset size affect training of sequence-to-function models from scATAC-seq. Out now www.nature.com/articles/s41... (details below)
nature.com
Evaluating single-cell ATAC-seq atlasing technologies using sequence-to-function modeling - Nature Communications
Generating high-quality training data for machine learning is costly. Here, authors include sequence-to-function modeling in benchmarking of custom and commercial droplet-based scATAC platforms, and r...
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Seppe De Winter @seppedewinter.bsky.social · 17/01/2026
For the motif enrichment analysis we already made use of cell type-specific ATAC peaks. So in that sense it already makes use of the data. But good suggestion to consider additional evaluations. Thank you!
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Seppe De Winter @seppedewinter.bsky.social · 17/01/2026
Thank you :). In this example we trained a new model only on PBMC scATAC-seq data using the CREsted framework.
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Reposted by Seppe De Winter
Stein Aerts @steinaerts.bsky.social · 15/01/2026
TF-MINDI is out! A new method to learn cis-regulatory codes through rich embeddings of TF binding sites. TF-MINDI decomposes motif neighbourhoods, and works downstream of any sequence-to-function deep learning model. We deeply study the enhancer code in human neural development, check out the thread
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
Check out the preprint: doi.org/10.64898/202... and the TF-MINDI package: github.com/aertslab/TF-MINDI. With @lukasmahieu.bsky.social ’s help this has become an amazing and user-friendly package, please give it a try and provide feedback.
doi.org
System-wide extraction of cis-regulatory rules from sequence-to-function models in human neural development
The genomic cis-regulatory code (CRC) underlies spatiotemporal specificity of gene expression. While sequence-to-function (S2F) models can accurately encode the CRC of transcriptional enhancers, decod...
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
I would like to thank my co-authors; @camielmannens.bsky.social for the embryo data and analysis together with @sten.linnarsson.org & Lijuan Hu. Valerie and Roel for all the experimental work. @steinaerts.bsky.social for supporting me through this long journey.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
Finally, using topic-modelling we model TFBS co-occurrences. We validate these white-box enhancer models by performing cross-species integration of our TF-MINDI results, with a zebrafish developmental S2F model, and show that the topic models can recover zebrafish floor plate-specific regions.
Top left: schematic representation of topic modeling. 1. A count matrix (heatmap) of pattern clusters instances across genomic regions is generated. 2. Topic modeling is performed. A schematic representation is shown illustrating that both topic-pattern probabilities and region-topic probabilities are simultaneously optimised in this procedure. 3. Once the model is generated now sequence can be scored by generating a new pattern-cluster by genomic region count matrix and scoring this using the topic model. 

Top right: Heatmap showing pattern-topic probabilities in organoid and embryo. Topic corresponding to floor plate cells (FP), pre-migratory neural crest (pre-mig. NC), migratory neural crest (mig. NC) and neurons (Neu) are highlighted. Under this heatmap another heatmap is shown for both organoid and embryo. This heatmap quantifies the correlation between accessibility based region topic probabilites and pattern based region topic probabilities.

Bottom left: tSNE dimensionality reduction of TF-MINDI instances from organoid, embryo and zebrafish. Instances are colored by dataset of origin and plot shows that they integrate well. TF-families are indicated with dashed lines.

bottom right top: Precision-recall curves of deepNeuralTube models, zebrafish models and pattern-topic probability models showing their accuracy of predicting floor plate specific regions in zebrafish. The pattern-topic models perform on par with the deepNeuralTube models.

bottom right bottom: Scatter plot showing that the average floor plate prediction score of the DeepNeuralTube models (x-axis) is correlated to the average floor plate pattern-region-topic probabilities (y-axis).
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
Implanting either two high affinity coordinator instances or a single coordinator instance together with 5 additional TF-MINDI TFBS is sufficient to generate new facial mesenchyme enhancers.
Left: Contribution score plot of six synthetic enhancers. Coordinator and non-coordinator instances are highlighted. Right: Bar chart showing luciferase activity of those synthetic enhancers. Plot shows that enhancers with either two high affinity coordinator instances or a single high affinity coordinator instances together with five additional instances are equally active. Enhancers containing only a single high affinity coordinator instance (and no additional binding sites) are less active.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
To test the sufficiency of the TF-MINDI extracted enhancer code rules we turn to synthetic enhancer design in facial mesenchyme cells. A homeobox-ebox dimer motif (Coordinator) has been shown to be instrumental for this cell type. TF-MINDI identified Coordinator instances at varying affinities.
tSNE dimensionality reduction of facial mesenchyme TF-MINDI seqlets colored based on TF-family. The coordinator instances are circled and an arrow drawn to a PCA of those coordinator instances colored based on coordinator motif score. This shows that TF-MINDI captures multiple coordinator affinities. For each affinity bin a TF binding motif logo is shown.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
We validate the TF-MINDI instances using ChIP-seq data in PBMC. Showing that TF-MINDI is more accurate compared to traditional motif enrichment analysis tools.
A large tSNE dimensionality reduction showing PBMC TF-MINDI seqlets colored based on TF-family. This is surrounded by four smaller tSNE dimensionality reductons colored based on TF-ChIP-seq Z-score. Showing specific enrichment of TFs in TF binding sites annotated to the family of that TF. Bottom right shows ROC curve, comparing TF-MINDi based prediction of ChIP-seq signal with motif enrichment based prediction (cisTarget). This shows that TF-MINDI is more accurate.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
Counting the number of TFBS instances across cell type-specific peaks reveals cell type-specific regulators in the form of a code-table. Similar codes are obtained for the organoid and embryo and we link instances to TFs based on cell type-specific TF-expression.
Figure showing three panels. Top: code table for organoid (left) and embryo (right). On the y-axis different TF-families; on the x-axis different cell type-specific regions. And a dotplot, where the dotsize represents the average number of instances of a TF-family for each cell type-specific peak and the color represents the average contribution per TF-family and cell type-specific peak. Bottom left: heatmap showing jaccard index quanitfying genomic overlap of organoid and embryo derived seqlets. Bottom right: Plot showing pearson correlation between TF-expression across cell types (x-axis) and average number of instances per cell type-specific peak (y-axis). A square is drawn whenever the pearson correlation coefficient > 0.35, and the color of the square represents the pearson correlation coefficient.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
To obtain high dimensional embeddings of S2F identified motifs, annotate TFBS across cell-type specific peaks and model TFBS co-occurrences we developed a new python package named TF-MINDI. Resulting in > 400k annotated TFBS instances across the genome (each dot in the tSNE below is one instance).
Figure showing four panels. Top left: TF-MNDI logo (pink background and yellow letters), showing the text: "Transcription Factor Motif Instance Neighborhood Decomposition and Interpretation". Top right: TF-MINDI workflow. 1. seqlets are called (showing nucleotide level contribution scores and seqlets as blocks of nucleotides with high contribution). 2. Seqlets are embedded (showing, for each seqlet, a representation of a vector as a heatmap) and 3 seqlets are clustered and annotated (showing a schematic representation of a dimensionality reduction with seqlets colored based on TF-families as well as TF binding motif logos). Bottom left, tSNE dimensionality reduction of organoid seqlets colored based on TF family. Bottom right, similar tSNE dimensionality reduction for embryo seqlets.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
We tackle this challenge in human neural development. We generate two multiome atlases: on neural tube organoids and on a 4 p.c.w. human embryo. The organoids recapitulate human embryonic development strikingly well. DeepNeuralTube S2F models recover most known cell type-specific TF binding motifs.
Two UMAP dimensionality reductions. One for neural tube organoids and the other for human embryo. The UMAP is colored based on cell type-identity.
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Seppe De Winter @seppedewinter.bsky.social · 15/01/2026
We are thrilled to share our new pre-print: “System-wide extraction of cis-regulatory rules from sequence-to-function models in human neural development”. S2F-deeplearning models can accurately encode enhancers, yet decoding these models into human-interpretable rules remains a major challenge.
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Alexandra P @alexanrna.bsky.social · 10/09/2025
1/ First preprint from @jdemeul.bsky.social lab 🥳! We present our new multi-modal single-cell long-read method SPLONGGET (Single-cell Profiling of LONG-read Genome, Epigenome, and Transcriptome)! www.biorxiv.org/content/10.1...
ikea-style logo of splongget
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Niklas Kempynck @niklaskemp.bsky.social · 21/05/2025
Check out our work on evaluating methods for predicting in vivo cell enhancer activity in the mouse cortex! Combined, scATAC peak specificity and sequence-based CREsted predictions gave the best predictive performance, aiming to advance genetic tool design for cell targeting in the brain.
cell.com
Evaluating methods for the prediction of cell-type-specific enhancers in the mammalian cortex
Johansen et al. report the results of a community challenge to predict functional enhancers targeting specific brain cell types. By comparing multi-omics machine learning approaches using in vivo data...
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Reposted by Seppe De Winter
Stein Aerts @steinaerts.bsky.social · 21/05/2025
One thousand candidate enhancers tested in vivo in the mouse brain! A massive resource and oh so useful as validation set for genome-wide enhancer prediction methods. Super fun to be involved in one of the papers: ‘the prediction challenge paper’ by Nelson&Niklas et al www.cell.com/cell-genomic...
cell.com
Evaluating methods for the prediction of cell-type-specific enhancers in the mammalian cortex
Johansen et al. report the results of a community challenge to predict functional enhancers targeting specific brain cell types. By comparing multi-omics machine learning approaches using in vivo data...
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Seppe De Winter @seppedewinter.bsky.social · 21/05/2025
Great! Thank you so much!
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Seppe De Winter @seppedewinter.bsky.social · 21/05/2025
Hi, looks very interesting! Any chance that you can share the manuscript, for example using www.springernature.com/gp/researche...?
springernature.com
SharedIt | Springer Nature | For Researchers | Springer Nature__small_youtube
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Seppe De Winter @seppedewinter.bsky.social · 24/04/2025
For those looking to read the article, it's available via this link rdcu.be/egQdA
rdcu.be
Modelling and design of transcriptional enhancers
Nature Reviews Bioengineering - Enhancers are genomic elements critical for regulating gene expression. In this Review, the authors discuss how sequence-to-function models can be used to unravel...
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Reposted by Seppe De Winter
Jacob Schreiber @jmschreiber91.bsky.social · 24/04/2025
Our preprint on designing and editing cis-regulatory elements using Ledidi is out! Ledidi turns *any* ML model (or set of models) into a designer of edits to DNA sequences that induce desired characteristics. Preprint: www.biorxiv.org/content/10.1... GitHub: github.com/jmschrei/led...
biorxiv.org
Programmatic design and editing of cis-regulatory elements
The development of modern genome editing tools has enabled researchers to make such edits with high precision but has left unsolved the problem of designing these edits. As a solution, we propose Ledi...
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Stein Aerts @steinaerts.bsky.social · 04/04/2025
Very proud of two new preprints from the lab: 1) CREsted: to train sequence-to-function deep learning models on scATAC-seq atlases, and use them to decipher enhancer logic and design synthetic enhancers. This has been a wonderful lab-wide collaborative effort. www.biorxiv.org/content/10.1...
biorxiv.org
CREsted: modeling genomic and synthetic cell type-specific enhancers across tissues and species
Sequence-based deep learning models have become the state of the art for the analysis of the genomic regulatory code. Particularly for transcriptional enhancers, deep learning models excel at decipher...
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Reposted by Seppe De Winter
Hannah Dickmänken @hannahdckmnkn.bsky.social · 04/04/2025
Our new preprint is out! We optimized our open-source platform, HyDrop (v2), for scATAC sequencing and generated new atlases for the mouse cortex and Drosophila embryo with 607k cells. Now, we can train sequence-to-function models on data generated with HyDrop v2! www.biorxiv.org/content/10.1...
Data collected with the new sequencing platform HyDrop v2 is shown. First, a schematic overview of the bead batches of the microfluidic beads is followed by a tSNE and a barplot showing the costs in comparison to 10x Genomics. 
Then, a track of mouse data (cortex) is shown together with nucleotide contribution scores in the FIRE enhancer in microglia. Here, the HyDrop and 10x based models show the same contributions. 
On the right, the Drosophila embryo collection is explained; in the paper HyDrop v2 and 10x data are compared to sciATAC data. Then, a nucleotide contribution score is also shown, whereas HyDrop v2 and 10x models show the same contribution, just as in mouse.
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Niklas Kempynck @niklaskemp.bsky.social · 03/04/2025
We released our preprint on the CREsted package. CREsted allows for complete modeling of cell type-specific enhancer codes from scATAC-seq data. We demonstrate CREsted’s robust functionality in various species and tissues, and in vivo validate our findings: www.biorxiv.org/content/10.1...
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Kaessmann Lab @kaessmannlab.bsky.social · 16/03/2025
How does gene regulation shape brain evolution? Our new preprint dives into this question in the context of mammalian cerebellum development! rb.gy/dbcxjz Led by @ioansarr.bsky.social, @marisepp.bsky.social and @tyamadat.bsky.social, in collaboration with @steinaerts.bsky.social
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Saez-Rodriguez Group @saezlab.bsky.social · 14/03/2025
📄 Update on our preprint about Gene Regulatory Net (GRN) benchmarking 📄 We have included the original and decoupled version of SCENIC+, added a new metric and two more databases. Dictys and SCENIC+ outperformed others, but still performed poorly in causal mechanistic tasks. doi.org/10.1101/2024... 👇
Performance of multimodal GRN inference methods. SCENIC+ and Dictys outperform others.
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Seppe De Winter @seppedewinter.bsky.social · 12/03/2025
Thank you! I'm glad you liked it :).
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Seppe De Winter @seppedewinter.bsky.social · 28/02/2025
We wrote a review article on modelling and design of transcriptional enhancers using sequence-to-function models. From conventional machine learning methods to CNNs and using models as oracles/generative AI for synthetic enhancer design! @natrevbioeng.bsky.social www.nature.com/articles/s44...
nature.com
Modelling and design of transcriptional enhancers - Nature Reviews Bioengineering
Enhancers are genomic elements critical for regulating gene expression. In this Review, the authors discuss how sequence-to-function models can be used to unravel the rules underlying enhancer activit...
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Aligning Science Across Parkinson's @asapresearch.parkinsonsroadmap.org · 13/02/2025
The latest Discover ASAP episode dives into "Cell Type Directed Design of Synthetic Enhancers," a study published in Nature by CRN Team Voet. They discuss how machine learning enables precise enhancer design for targeted gene expression 🧬 Watch: www.youtube.com/watch?v=Qcms...
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VIB.AI @vibai.bsky.social · 14/02/2025
KU Leuven turns 600(!) this year and is celebrating with a public event this weekend! The @steinaerts.bsky.social lab is offering guided lab tours. Want a behind-the-scenes look? All tours on Saturday are full, but you can still register for Sunday! www.kuleuven.be/600years/exp...
kuleuven.be
Explore cellular diversity with microscopy and AI: registration | KU Leuven
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VIB.AI @vibai.bsky.social · 14/02/2025
In a new study, Nikolai Hecker, Niklas Kempynck et al. in the team of @steinaerts.bsky.social explore 300 million years of brain evolution through the lens of enhancer codes. www.science.org/doi/10.1126/...
science.org
Enhancer-driven cell type comparison reveals similarities between the mammalian and bird pallium
Combinations of transcription factors govern the identity of cell types, which is reflected by genomic enhancer codes. We used deep learning to characterize these enhancer codes and devised three metr...
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Stein Aerts @steinaerts.bsky.social · 14/02/2025
This has been a fantastic adventure - to capture the genomic regulatory code underlying brain cell types (using deep learning models trained on chromatin accessibility), and then use these models to compare cell types between the bird and mammalian brain
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Niklas Kempynck @niklaskemp.bsky.social · 14/02/2025
Just very happy to have our paper out today! A big thanks to all our co-authors, and to Nikolai and @steinaerts.bsky.social for the teamwork over the past years. If you are interested in using our models for cross-species enhancer studies, check out crested.readthedocs.io/en/stable/mo... 🙂
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