Pith. sign in

REVIEW 2 cited by

DiscoGen: Learning to Discover Gene Regulatory Networks

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2304.05823 v1 pith:GYDHL5ZU submitted 2023-04-12 q-bio.MN cs.LGq-bio.GN

classification q-bio.MNcs.LGq-bio.GN
keywords discoverycausaldatamethodsgenegrnsnetwork-basedneural
verification ladder T0 review T1 audit T2 compute T3 formal

Signed reviews

No signed human review yet.

0 comments
read the original abstract

Accurately inferring Gene Regulatory Networks (GRNs) is a critical and challenging task in biology. GRNs model the activatory and inhibitory interactions between genes and are inherently causal in nature. To accurately identify GRNs, perturbational data is required. However, most GRN discovery methods only operate on observational data. Recent advances in neural network-based causal discovery methods have significantly improved causal discovery, including handling interventional data, improvements in performance and scalability. However, applying state-of-the-art (SOTA) causal discovery methods in biology poses challenges, such as noisy data and a large number of samples. Thus, adapting the causal discovery methods is necessary to handle these challenges. In this paper, we introduce DiscoGen, a neural network-based GRN discovery method that can denoise gene expression measurements and handle interventional data. We demonstrate that our model outperforms SOTA neural network-based causal discovery methods.

Discussion (0). Continue with ORCID to comment.

Forward citations

Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. No Foundations without Foundations -- Why semi-mechanistic models are essential for regulatory biology

    cs.LG 2025-01 conditional novelty 6.0 of 10

    A semi-mechanistic model of CRISPR perturbation screens, built from editing, media, and waiting operations, improves gene-expression prediction when trained with an extra steady-state constraint.

  2. The Landscape of Causal Discovery Data: Grounding Causal Discovery in Real-World Applications

    cs.LG 2024-12 conditional novelty 5.0 of 10

    A systematic review showing causal discovery evaluation is still dominated by small, low-diversity datasets and structural metrics, with a curated set of realistic alternatives.

Pith tools