Evidence map›Paper›PMID 41383407›Full record

ArticleBioinformatics advances2025

ntRoot: computational inference of human ancestry at scale from genomic data.

René L Warren, Lauren Coombe, Johnathan Wong, Parham Kazemi, Inanc Birol

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

René L WarrenCanada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, V5Z 4S6, Canada.ORCID https://orcid.org/0000-0002-9890-2293
Lauren CoombeCanada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, V5Z 4S6, Canada.ORCID https://orcid.org/0000-0002-7518-2326
Johnathan WongCanada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, V5Z 4S6, Canada.ORCID https://orcid.org/0000-0002-1687-8972
Parham KazemiCanada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, V5Z 4S6, Canada.ORCID https://orcid.org/0000-0002-2126-5644
Inanc BirolCanada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, V5Z 4S6, Canada.ORCID https://orcid.org/0000-0003-0950-7839

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Ancestry information is essential to large cohort studies but is often unavailable or inconsistently measured. For studies involving genome sequencing, existing ancestry prediction methods are constrained by computational demands and complex input requirements. Efficient, scalable approaches are needed to infer ancestry directly from sequencing data while maintaining accuracy and reproducibility. Results: We present ntRoot, a computationally lightweight method for inferring human super-population-level ancestry from whole genome assemblies or short or long sequencing data. Utilizing a reference-guided, alignment-free single nucleotide variant detection framework, ntRoot employs a succinct Bloom filter to efficiently query diverse genomic inputs against a variant reference panel with known genotypes and ancestry. Demonstrated on over 600 human genome samples, including complete genomes, draft assemblies, and 280 independently generated samples, ntRoot accurately predicts geographic labels and shows high concordance with traditional methods such as ADMIXTURE ( Availability: ntRoot is freely available on GitHub (https://github.com/bcgsc/ntroot).

Identifiers

PMID41383407
PMCPMC12695050

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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.