Evidence map›Paper›PMID 42093749›Full record

ArticleGigaByte (Hong Kong, China)2026

Efficient downsampling of genome alignments with Rasusa.

Achmad Dimas Cahyaning Furqon, Leah W Roberts, Michael B Hall

Abstract read
In one paragraph

Article in GigaByte (Hong Kong, China), 2026. 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

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.

Achmad Dimas Cahyaning FurqonThe University of Queensland, UQ Centre for Clinical Research, QLD 4029, Herston, Australia.ORCID https://orcid.org/0009-0007-8039-1951
Leah W RobertsThe University of Queensland, UQ Centre for Clinical Research, QLD 4029, Herston, Australia.ORCID https://orcid.org/0000-0002-1024-0564
Michael B HallThe University of Queensland, UQ Centre for Clinical Research, QLD 4029, Herston, Australia.ORCID https://orcid.org/0000-0003-3683-6208

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput sequencing datasets frequently exhibit extreme read depth variation, biasing downstream analysis. Normalising coverage to a specific depth cap is important, yet existing tools rely on computationally expensive fetch-based or non-deterministic greedy algorithms. Here, we present a new coordinate-sorted sweep-line algorithm implemented in the open-source software rasusa that enforces a strict coverage cap at every genomic position. By utilising seeded random priority assignment, we achieve unbiased, reproducible read selection. The algorithm reduces runtimes by over 1,400-fold compared to legacy fetch-based methods-slashing processing from hours to mere seconds-and operates roughly four times faster than VariantBam. Furthermore, it requires only 8 MB of memory for long-read data. This provides a highly efficient, scalable, and reproducible solution for sequencing coverage normalisation.

Identifiers

PMID42093749
PMCPMC13141811

What OpenQuestion holds

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LicenceCC BY
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.