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Melanie Weilert

@mlweilert.bsky.social

bioinformatics, cats, deep learning, genomics, Zeitlinger Lab ((all views are mine alone))

50 Followers  |  136 Following  |  3 Posts  |  Joined: 28.01.2025  |  1.6371

Latest posts by mlweilert.bsky.social on Bluesky

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Evolution and core processes in gene expression June 26–29, 2025 | Kansas City, Mo.

Like regulatory genomics? Don’t miss this very fun meeting! May 7 is the deadline for early registration and abstract submission www.asbmb.org/meetings-eve...

07.05.2025 01:57 β€” πŸ‘ 15    πŸ” 5    πŸ’¬ 0    πŸ“Œ 2
From the BioRxiv pre-print article "Long-range massively parallel reporter assay reveals rules of distal enhancer-promoter interactions" by Yawei Wu et al. 
Fig. 1. Design of long-range MPRA. a, Design of the enhancer landing pad and the promoter landing
pad. The enhancer landing pad contains a dual promoter driving expression of an mTagBFP fluorescent
protein and a thymidine kinase (TK) gene for counterselection, flanked by FRT and F3 sites for RMCE.
available under aCC-BY-NC 4.0 International license.
was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made
bioRxiv preprint doi: https://doi.org/10.1101/2025.04.21.649048; this version posted April 22, 2025. The copyright holder for this preprint (which
The promoter landing pad expresses the mEmerald fluorescent protein and iCaspase9 for
counterselection and is flanked by loxFAS and loxP sites for orthogonal RMCE. b-c, Workflow of
long-range MPRA. eBC: enhancer barcode; rBC: random barcode; dBC: distance barcode. A barcoded
enhancer library is integrated into pooled long-range landing pad cells through Flpase-facilitated
recombination. After counterselection with Ganciclovir, cells with successful integration are enriched.
Cells are sorted into different bins based on mScarlet fluorescence level. Genomic DNA is extracted from
each bin; barcodes are amplified and sequenced. Reporter gene expression of each enhancer at each
distance is calculated as the weighted average of fluorescence levels across bins.

From the BioRxiv pre-print article "Long-range massively parallel reporter assay reveals rules of distal enhancer-promoter interactions" by Yawei Wu et al. Fig. 1. Design of long-range MPRA. a, Design of the enhancer landing pad and the promoter landing pad. The enhancer landing pad contains a dual promoter driving expression of an mTagBFP fluorescent protein and a thymidine kinase (TK) gene for counterselection, flanked by FRT and F3 sites for RMCE. available under aCC-BY-NC 4.0 International license. was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made bioRxiv preprint doi: https://doi.org/10.1101/2025.04.21.649048; this version posted April 22, 2025. The copyright holder for this preprint (which The promoter landing pad expresses the mEmerald fluorescent protein and iCaspase9 for counterselection and is flanked by loxFAS and loxP sites for orthogonal RMCE. b-c, Workflow of long-range MPRA. eBC: enhancer barcode; rBC: random barcode; dBC: distance barcode. A barcoded enhancer library is integrated into pooled long-range landing pad cells through Flpase-facilitated recombination. After counterselection with Ganciclovir, cells with successful integration are enriched. Cells are sorted into different bins based on mScarlet fluorescence level. Genomic DNA is extracted from each bin; barcodes are amplified and sequenced. Reporter gene expression of each enhancer at each distance is calculated as the weighted average of fluorescence levels across bins.

🚨PRE-PRINT πŸ§ͺ🧬πŸ–₯οΈπŸ‘©β€πŸ”¬
Long-range massively parallel reporter assay reveals rules of distal enhancer-promoter interactions
From Barak Cohen's lab at @washu.bsky.social

Read the pre-print πŸ‘‡
doi.org/10.1101/2025...
Learn more about the research from the Cohen lab: bclab.wustl.edu

23.04.2025 20:43 β€” πŸ‘ 11    πŸ” 5    πŸ’¬ 1    πŸ“Œ 1

Our new preprint is out! Want to better visualize what your sequence-to-function profile learned? Here is PISA. It also comes in a new BPNet package, which can be used to train many genomics data sets, including MNase-seq data.

08.04.2025 13:31 β€” πŸ‘ 26    πŸ” 8    πŸ’¬ 1    πŸ“Œ 0
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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...

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...

04.04.2025 09:04 β€” πŸ‘ 109    πŸ” 39    πŸ’¬ 5    πŸ“Œ 1
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We're thrilled that Investigator @juliazeitlinger.bsky.social is co-chairing the 2025 @asbmb.bsky.social meeting in #KansasCity, which will delve into the core processes of #geneexpression from #developmental and evolutionary perspectives.

Read more: bit.ly/41Czvqy

03.03.2025 21:31 β€” πŸ‘ 8    πŸ” 3    πŸ’¬ 0    πŸ“Œ 1

This a great interdisciplinary gene expression meeting, where everyone is welcome. Please consider attending and submitting your abstract: www.asbmb.org/meetings-eve...

04.03.2025 14:10 β€” πŸ‘ 12    πŸ” 6    πŸ’¬ 0    πŸ“Œ 1

dear god

23.02.2025 14:44 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Or just rename every one to start with B. Bavocado, Bragonfruit, Bomegranate 🀭

19.02.2025 01:53 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
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Thermodynamic principles link in vitro transcription factor affinities to single-molecule chromatin states in cells The molecular details governing transcription factor (TF) binding and the formation of accessible chromatin are not yet quantitatively understood - including how sequence context modulates affinity, h...

Thermodynamic principles link in vitro transcription factor affinities to singlemolecule chromatin states in cells

www.biorxiv.org/content/10.1...

30.01.2025 17:12 β€” πŸ‘ 29    πŸ” 12    πŸ’¬ 0    πŸ“Œ 0

5 minutes on this platform and it's already clear leaving Twitter was a great call, glad to see everyone <3

29.01.2025 00:35 β€” πŸ‘ 4    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

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