Evidence map›Paper›PMID 38260359›Full record

ArticlebioRxiv : the preprint server for biology2024

Detecting m6A RNA modification from nanopore sequencing using a semi-supervised learning framework.

Haotian Teng, Marcus Stoiber, Ziv Bar-Joseph, Carl Kingsford

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

4 authors.

Haotian TengComputational Biology Department, Carnegie Mellon Univeristy, Pittsburgh PA 15213, USA.ORCID 0000-0003-0337-8722
Marcus StoiberOxford Nanopore Technologies.
Ziv Bar-JosephComputational Biology Department, Carnegie Mellon Univeristy, Pittsburgh PA 15213, USA.ORCID 0000-0003-3430-6051
Carl KingsfordComputational Biology Department, Carnegie Mellon Univeristy, Pittsburgh PA 15213, USA.ORCID 0000-0002-0118-5516

Funding

Improved genomic sketching for MUMmer and metagenomicsR01HG012470 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE, MARÇAIS, GUILLAUME · 2022 to 2025
$1.7M
NHGRI NIH HHS R01 HG012470
6 · The paper itself

Abstract

Direct nanopore-based RNA sequencing can be used to detect post-transcriptional base modifications, such as m6A methylation, based on the electric current signals produced by the distinct chemical structures of modified bases. A key challenge is the scarcity of adequate training data with known methylation modifications. We present Xron, a hybrid encoder-decoder framework that delivers a direct methylation-distinguishing basecaller by training on synthetic RNA data and immunoprecipitation-based experimental data in two steps. First, we generate data with more diverse modification combinations through in silico cross-linking. Second, we use this dataset to train an end-to-end neural network basecaller followed by fine-tuning on immunoprecipitation-based experimental data with label-smoothing. The trained neural network basecaller outperforms existing methylation detection methods on both read-level and site-level prediction scores. Xron is a standalone, end-to-end m6A-distinguishing basecaller capable of detecting methylated bases directly from raw sequencing signals, enabling de novo methylome assembly.

Indexed as

Deep learninghidden Markov modelm6A RNA modificationNanopore sequencing

Identifiers

PMID38260359
PMCPMC10802372

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
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.