Evidence map›Paper›PMID 41213983›Full record

ArticleScientific reports2025

Motif caller for sequence reconstruction in motif-based DNA storage.

Parv Agarwal, Nimesh Pinnamaneni, Thomas Heinis

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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

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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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Parv AgarwalDepartment of Computing, Imperial College London, London, UK. p.agarwal23@imperial.ac.uk.
Nimesh PinnamaneniHelixworks Technologies, Cork, Ireland.
Thomas HeinisDepartment of Computing, Imperial College London, London, UK.

Funding

HORIZON EUROPE European Research Council 101115389
6 · The paper itself

Abstract

DNA data storage is rapidly emerging as a promising solution for long-term data archiving, largely due to its exceptional durability. However, the synthesis of DNA strands remains a significant bottleneck in terms of cost and speed. To address this, new methods have been developed that encode information by concatenating long data-carrying DNA sequences from pre-synthesized DNA subsequences - known as motifs - from a library. Reading back data from DNA storage relies on basecalling-the process of translating raw nanopore sequencing signals into DNA base sequences using machine learning models. These sequences are then decoded back into binary data. However, current basecalling approaches are not optimized for decoding motif-carrying DNA: they first predict individual bases from the raw signal and only afterward attempt to identify higher-level motifs. This two-step, motif-agnostic process is both imprecise and inefficient. In this paper we introduce Motif Caller, machine learning model designed to directly detect entire motifs from raw nanopore signals, bypassing the need for intermediate basecalling. By targeting motifs directly, Motif Caller leverages richer signal features associated with each motif, resulting in significantly improved accuracy. This direct approach also enhances the efficiency of data retrieval in motif-based DNA storage systems.

Indexed as

DNAInformation Storage and RetrievalNucleotide MotifsSequence Analysis, DNAAlgorithmsBase SequenceMachine LearningNanopore SequencingDNA

Identifiers

PMID41213983
PMCPMC12603312

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Registered trials

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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.