Generating long deletions across the genome with pooled paired prime editing screens
Engineered deletions are a powerful probe for studying genome architecture, function, and regulation. Yet, the lack of effective methods to create them in large numbers and at multi-kilobase scale has...
New ๐งฌโ๏ธ pre-print! We show that paired prime editing can efficiently generate large deletions โ even >1 Mb โ with high precision and at scale. We use this to perform the first pooled prime deletion screen across the human genome.
๐ biorxiv.org/content/10.1...
A short thread (by Juliane Weller)๐
05.11.2025 14:17 โ ๐ 43 ๐ 19 ๐ฌ 3 ๐ 2
I have more features planned to support my work, for instance multiple constructs in one library, combinations of sub-libraries and a region type expecting variants to a base sequence, but issues and pull-requests with other bugs and suggestions are very welcome too.
13.10.2025 14:35 โ ๐ 0 ๐ 0 ๐ฌ 1 ๐ 0
Simulated tests and benchmarks and our datasets suggest the tool is generally accurate and robust as well as pretty quick. Feels like a state that could be useful more widely so a good time to share, although I do expect more bugs to come out with wider usage!
13.10.2025 14:35 โ ๐ 0 ๐ 0 ๐ฌ 1 ๐ 0
Currently position in reads, flanking patterns and full alignment can be used to extract regions and extact matching, hamming distance and (bounded) Levenshtein used to compare to your library. This lets you nicely balance match accuracy with speed for your design.
13.10.2025 14:35 โ ๐ 2 ๐ 0 ๐ฌ 1 ๐ 0
It takes in (paired) fastq/a files, a JSON expected read structure, an optional expected combinations TSV and a strategy for extracting and matching variable regions and outputs count tables against your library.
13.10.2025 14:35 โ ๐ 0 ๐ 0 ๐ฌ 1 ๐ 0
GitHub - allydunham/dnacomb: CLI tool for flexibly parsing structured sequence reads into count tables and comparing them to expected libraries
CLI tool for flexibly parsing structured sequence reads into count tables and comparing them to expected libraries - allydunham/dnacomb
We've been screening across many DNA construct structures with variable number/size of interesting regions - e.g. spacer, extension and barcode for prime editing. There wasn't a widely used tool to process these complex structured reads so I ended up developing github.com/allydunham/d....
13.10.2025 14:35 โ ๐ 6 ๐ 3 ๐ฌ 1 ๐ 0
MPRAbase a Massively Parallel Reporter Assay database
An international, peer-reviewed genome sciences journal featuring outstanding original research that offers novel insights into the biology of all organisms
MPRAbase (mprabase.ucsf.edu) , a customized database for massively parallel reporter assays (MPRAs) to easily find and download MPRA data. Amazing work by Jingjing Zhao, Fotis Baltoumas, Georgios Pavlopoulos, @vagar.bsky.social, ilias Georgakopoulos-Soares & others.
genome.cshlp.org/content/earl...
22.04.2025 20:51 โ ๐ 30 ๐ 10 ๐ฌ 0 ๐ 0
We're hiring to expand on the work to understand the human genome by engineering it!
lnkd.in/da-gitNc
10.02.2025 08:53 โ ๐ 12 ๐ 8 ๐ฌ 0 ๐ 0
Enhancer scrambling strategy
We are happy to share our enhancer scramble story, a strategy to create hundreds of stochastic deletions, inversions, and duplications within mammalian gene regulatory regions and associate these new architectures with gene expression levels ๐งต
www.biorxiv.org/content/10.1...
15.01.2025 20:32 โ ๐ 182 ๐ 77 ๐ฌ 3 ๐ 2
LinkedIn
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Does my mutation have the same impact as yours? Population genetics ๐ค ๐ฅธ ๐ค ๐คก meets single cell CRISPRi โก ! www.biorxiv.org/content/10.1... Led by Claudia Feng, Oliver Stegle, Britta Velten, @sangerinstitute.bsky.social .
02.12.2024 13:57 โ ๐ 58 ๐ 24 ๐ฌ 2 ๐ 3
Postdoc in Lars Velten's lab @crg.eu, working on gene regulation in haematopoiesis using ML techniques
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Cancer Research UK Career Development Fellow at the Wellcome Sanger Institute - gene editing - drug resistance - cancer