Evidence map›Paper›PMID 38405704›Full record

ArticlebioRxiv : the preprint server for biology2024

Evaluation and optimization of sequence-based gene regulatory deep learning models.

Abdul Muntakim Rafi, Daria Nogina, Dmitry Penzar, Dohoon Lee, Danyeong Lee, Nayeon Kim, Sangyeup Kim, Dohyeon Kim, Yeojin Shin, Il-Youp Kwak and 16 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

Abdul Muntakim RafiUniversity of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-0387-5430
Daria NoginaLomonosov Moscow State University, Moscow, Russia.ORCID 0000-0002-0593-2726
Dmitry PenzarLomonosov Moscow State University, Moscow, Russia.ORCID 0000-0001-7960-9385
Dohoon LeeSeoul National University, Seoul, South Korea.ORCID 0000-0003-2163-5489
Danyeong LeeSeoul National University, Seoul, South Korea.
Nayeon KimSeoul National University, Seoul, South Korea.ORCID 0000-0003-1222-8742
Sangyeup KimSeoul National University, Seoul, South Korea.
Dohyeon KimSeoul National University, Seoul, South Korea.
Yeojin ShinSeoul National University, Seoul, South Korea.
Il-Youp KwakChung-Ang University, Seoul, South Korea.ORCID 0000-0002-7117-7669
Georgy MeshcheryakovInstitute of Protein Research, Russian Academy of Sciences, Pushchino, Russia.
Andrey LandoYandex N. V., Moscow, Russia.
Arsenii ZinkevichLomonosov Moscow State University, Moscow, Russia.
Byeong-Chan KimChung-Ang University, Seoul, South Korea.
Juhyun LeeChung-Ang University, Seoul, South Korea.
Taein KangChung-Ang University, Seoul, South Korea.
Eeshit Dhaval VaishnavBroad Institute of MIT and Harvard, Massachusetts, United States.ORCID 0000-0003-3720-8051
Payman YadollahpourBroad Institute of MIT and Harvard, Massachusetts, United States.
Random Promoter DREAM Challenge Consortium
Sun KimSeoul National University, Seoul, South Korea.ORCID 0000-0001-5385-9546
Jake AlbrechtSage Bionetworks.
Aviv RegevBroad Institute of MIT and Harvard, Massachusetts, United States.
Wuming GongUniversity of Minnesota, Minneapolis, United States.ORCID 0000-0002-3147-4028
Ivan V KulakovskiyVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.ORCID 0000-0002-6554-8128
Pablo MeyerHealth Care & Life Sciences, IBM Research.ORCID 0000-0001-5281-4661
Carl de BoerUniversity of British Columbia, Vancouver, BC, Canada.ORCID 0000-0001-8935-5921

Funding

Advancing method benchmarking and data sharing through crowd-sourced competitions in cancer researchU24CA248265 · NCI · SAGE BIONETWORKS · PI BOUTROS, PAUL CHRISTOPHER, VARMA, SUSHEEL · 2020 to 2024
$4.1M
Learning the rules of enhancer activity to understand non-coding genetic variation in autoimmune diseaseK99HG009920 · NHGRI · BROAD INSTITUTE, INC. · PI DE BOER, CARL · 2018 to 2019
$211k
NCI NIH HHS U24 CA248265NHGRI NIH HHS K99 HG009920
6 · The paper itself

Abstract

Neural networks have emerged as immensely powerful tools in predicting functional genomic regions, notably evidenced by recent successes in deciphering gene regulatory logic. However, a systematic evaluation of how model architectures and training strategies impact genomics model performance is lacking. To address this gap, we held a DREAM Challenge where competitors trained models on a dataset of millions of random promoter DNA sequences and corresponding expression levels, experimentally determined in yeast, to best capture the relationship between regulatory DNA and gene expression. For a robust evaluation of the models, we designed a comprehensive suite of benchmarks encompassing various sequence types. While some benchmarks produced similar results across the top-performing models, others differed substantially. All top-performing models used neural networks, but diverged in architectures and novel training strategies, tailored to genomics sequence data. To dissect how architectural and training choices impact performance, we developed the

Identifiers

PMID38405704
PMCPMC10888977

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.