BiologybioRxiv
Ranked by formulaVerdict: NotableReference mapping and whole-genome alignment yield comparable phylogenomic inferences
Reference-genome choice can introduce mapping bias when sequencing data are analysed against a heterospecific genome, but it remains unclear how strongly this bias affects species-level phylogenomic inference.
Caveats
- Preprint; not yet peer reviewed.
VerdictWorth a reader's time today.
Abstract
Reference-genome choice can introduce mapping bias when sequencing data are analysed against a heterospecific genome, but it remains unclear how strongly this bias affects species-level phylogenomic inference. We tested this across Ursidae using nine species spanning approximately 20 million years of divergence, including the extinct giant short-faced bear (Arctodus simus). We independently mapped the same sequencing datasets to four reference genomes spanning a broad range of evolutionary distances and compared these with two assembly-based whole-genome-alignment approaches. We developed PhyloSlide to analyse all treatments consistently, offering a streamlined pipeline for sliding-window phylogenomics. Using this approach, we found that mapping reference choice strongly affected sequence recovery, with missing data generally increasing with evolutionary distance. Nonetheless, all six treatments recovered an identical species-tree topology and highly similar gene and site concordance factors. Relative divergence-time estimates were also largely consistent between approaches. Together, these findings demonstrate that mapping sequencing reads from multiple species to a shared reference genome can yield phylogenomic inferences comparable to whole-genome alignment, despite substantial reference-dependent sequence loss across millions of years of evolutionary divergence.
The editor's rubric
- Leverage3 / 5
- A method or resource many groups across the field will adopt within a year.
- Magnitude2 / 5
- Solid incremental gain on a meaningful problem.
- Evidence3 / 5
- Solid: multiple benchmarks or cohorts, ablations, fair baselines, released code or data.
- Novelty2 / 5
- A new combination of known ideas.
- Trajectory3 / 5
- A clear path to scale.
- Stakes3 / 5
- Meaningful benefit to many people within a few years.
Editor’s rationale
Heuristic triage from title and abstract text only, not a reading of the paper. Cues found: breadth (wide range, many tasks); verification (multiple benchmarks, independent replication); stakes (global scale, prevention or cure).
How the score was computed
Desks place stronger verdicts first, then use this score to order work within the same verdict.
- Merit
- 5.3 / 10
- Adjusted merit
- 4.5 / 10
- Attention
- 0%
- Freshness
- 88%