Evidence map›Paper›PMID 41083943›Full record

ArticleBMC bioinformatics2025

Prior knowledge on context-driven DNA fragmentation probabilities can improve de novo genome assembly algorithms.

Patrick Pflughaupt, Aleksandr B Sahakyan

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

2 authors.

Patrick PflughauptRadcliffe Department of Medicine, MRC WIMM Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, OX3 9DS, UK.
Aleksandr B SahakyanRadcliffe Department of Medicine, MRC WIMM Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, OX3 9DS, UK. aleksandr.sahakyan@imm.ox.ac.uk.

Funding

UK MRC, MRC Strategic Alliance Funding MC UU 12025
6 · The paper itself

Abstract

backgroundDe novo genome assembly poses challenges when dealing with highly degraded DNA samples or ultrashort sequencing reads. Probabilistic approaches have been offered to enhance the algorithms, though existing methods rely solely on expected k-meric frequencies in the assemblies, neglecting the broader sequence context that strongly influences DNA fragmentation patterns.

resultsHere, we present a proof of concept showing that prior knowledge on sequence context-driven DNA breakage propensities, through the dedicated parameterisation of k-mer assigned breakage probabilities, can be utilised to recover DNA assemblies that originate from fragmentation patterns more likely to have happened. Our approach is beneficial even for read lengths below the common ∼ 25 bp threshold of modern de novo genome assembly algorithms, and well below the threshold used for ultrashort fragments used in ancient DNA research.

conclusionsThis work could lay the groundwork for future enhanced de novo genome assembly algorithms, with improved ability to effectively assemble and evaluate ultrashort DNA fragments relevant for cell-free, ancient, and forensic DNA research.

Indexed as

AlgorithmsDNADNA FragmentationGenomeGenomicsSequence Analysis, DNAHumansDNAContigsDe novo genome assemblyDNA breakageGenome fragmentationGenome simulations

Identifiers

PMID41083943
PMCPMC12519797

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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.