David Kelley
@drkbio.bsky.social
140 followers 57 following 54 posts
Making sophisticated guesses at how DNA will behave.
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drkbio.bsky.social
Will this recipe work for other organisms? We think it depends on genome size and proportion of nucleotides under selection, which drives the value of the self-supervised stage and training data scale. An exciting question for future work!
drkbio.bsky.social
This was a massive effort, driven by the incredible work of Calico intern Kuan-Hao Chao (@kuanhaochao.bsky.social
). Huge thanks to him, Majed Mohamed Magzoub, and Johannes Linder!
drkbio.bsky.social
My take: While MPRAs are powerful, they lose vital genomic context like local chromatin and post-transcriptional regulation. For modeling complex gene regulation in vivo, models trained on endogenous sequences are essential.
drkbio.bsky.social
Each wins on its “home field”:
* MPRA-trained models excel at predicting MPRA data, including variant sequences.
* Shorkie excels at predicting expression from promoters in their natural genomic context and eQTLs.
drkbio.bsky.social
How does Shorkie compare to models trained on massively parallel reporter assays (MPRAs)?
drkbio.bsky.social
This translates to variant effect prediction where Shorkie accurately predicts the impact of cis-eQTLs, outperforming alternative models at classifying influential regulatory variants.
drkbio.bsky.social
Shorkie also captures dynamic regulatory changes. Using new time-course RNA-seq data from TF inductions, we showed Shorkie can track how the importance of specific TF motifs changes over time.
drkbio.bsky.social
This pre-training strategy makes a huge difference. Shorkie substantially outperforms the same model trained from scratch, boosting gene-level expression prediction from a Pearson's R of 0.74 to 0.88.
drkbio.bsky.social
But which genomes work best? We trained on different phylogenetic levels, from close S. cerevisiae strains to the fungal kingdom. The Saccharomycetales order was the sweet spot, providing the right balance of diversity and conserved regulatory grammar for the model to learn from.
drkbio.bsky.social
Our hypothesis: Jumpstart supervised learning with self-supervision--before predicting chromatin and expression, we first asked our model to predict masked-out nucleotides across many related genomes, so it learns conserved elements like genes and their promoters.
drkbio.bsky.social
However, yeast's small genome provides limited data, making it tough for deep learning models to learn complex regulatory rules from scratch.
drkbio.bsky.social
At Calico, we've been studying S. cerevisiae for years to understand replicative aging. Along the way, we've generated rich datasets to probe its regulatory networks, which helped make this work possible.
drkbio.bsky.social
We’ve done some experiments, but the metrics aren’t conclusive, so choose your own adventure! We’ve released these models open source, open weight for all to use. github.com/calico/borzo...
borzoi-paper/extensions/prime at main · calico/borzoi-paper
Analyses related to the Borzoi paper. Contribute to calico/borzoi-paper development by creating an account on GitHub.
github.com
drkbio.bsky.social
We hypothesized that training with cell-type-specific and 3' data might make these models particularly effective for transfer to datasets with similar properties.
drkbio.bsky.social
Transfer learning has emerged as a key application for multitask sequence models like these. For more, check out another recent paper from Han Yuan, whose analysis explores various transfer strategies and shows how powerful this approach can be. www.biorxiv.org/content/10.1...
Parameter-Efficient Fine-Tuning of a Supervised Regulatory Sequence Model
DNA sequence deep learning models accurately predict epigenetic and transcriptional profiles, enabling analysis of gene regulation and genetic variant effects. While large-scale training models like E...
www.biorxiv.org
drkbio.bsky.social
Hence the name: Borzoi Prime to emphasize their 3’ expertise!
drkbio.bsky.social
Indeed, he discovered the new models better predict alternative polyadenylation and QTL variants that affect where transcripts get cleaved and polyadenylated. This key regulatory layer influences cell type-specific protein production.
drkbio.bsky.social
Drawing on his expertise and interest in isoform regulation, Johannes hypothesized that single-cell RNA-seq’s 3’ sequencing protocols might reveal additional capabilities in these models.
drkbio.bsky.social
Using single cell eQTL studies, he evaluated the cell type specific variant effect predictions and found good concordance.
drkbio.bsky.social
As cell-type-specific applications emerged, Johannes Linder took a fresh look.
drkbio.bsky.social
We trained these models in early 2023 (which is why they’re algorithmically similar to the originals), but initial metrics were underwhelming, so we shelved them.
drkbio.bsky.social
Side note—want your amazing data included in future training runs of open source, open weight models? Make and release BigWig tracks!
drkbio.bsky.social
We curated several cell atlas collections to produce pseudobulk coverage tracks. Thank you to the CZI Tabula projects and the BICCN Brain Cell Atlas for making this possible!