Evidence map›Paper›PMID 41262969›Full record

ArticleBioinformatics advances2025

FastGA: fast genome alignment.

Gene Myers, Richard Durbin, Chenxi Zhou

Abstract read
In one paragraph

Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Accelerating minimap2 for whole-genome alignment.Bioinformatics (Oxford, England) · 2026
    Article
  3. Adaptive Tracepoints for Pangenome Alignment Compression.bioRxiv : the preprint server for biology · 2026
    Article
  4. The complete genome of a songbird.bioRxiv : the preprint server for biology · 2025
    Article
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.

Gene MyersOkinawa Institute of Science and Technology, Onna-son, Okinawa 904-0495, Japan.ORCID https://orcid.org/0000-0002-6580-7839
Richard DurbinWellcome Sanger Institute, Hinxton CB10 1SA, United Kingdom.ORCID https://orcid.org/0000-0002-9130-1006
Chenxi ZhouDepartment of Genetics, Wellcome Sanger Institute, Cambridge CB2 3EH, United Kingdom.ORCID https://orcid.org/0000-0002-1735-2630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: FastGA finds alignments between two genome sequences more than an order of magnitude faster than previous methods that have comparable sensitivity. Its speed is due to (i) a fully Results: For example, two 2 Gbp bat genomes are compared in 2.1 min with eight threads on an Apple laptop using 5.7 GB of memory and producing 1.05 million alignments covering 60% of each genome. Our ALN format file occupies 66 MB and in just 6 s can be converted to a standard 1.03 GB PAF file. Availability and implementation: FastGA is freely available at GitHub: http://www.github.com/thegenemyers/FASTGA along with utilities for viewing inputs, intermediates, and outputs and transforming ALN files to PSL or PAF with or without CIGAR strings and common formats. There is also a utility to chain FastGA's alignments and display them in a dot-plot view in PostScript files.

Identifiers

PMID41262969
PMCPMC12624442

What OpenQuestion holds

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LicenceCC BY
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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.