Evidence map›Paper›PMID 33585906›Full record

ArticleGenome biology and evolution2021

A Chromosome-Painting-Based Pipeline to Infer Local Ancestry under Limited Source Availability.

Ludovica Molinaro, Davide Marnetto, Mayukh Mondal, Linda Ongaro, Burak Yelmen, Daniel John Lawson, Francesco Montinaro, Luca Pagani

Abstract readEvaluation Study
In one paragraph

Article in Genome biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
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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

8 authors.

Ludovica MolinaroEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Davide MarnettoEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Mayukh MondalEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Linda OngaroEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Burak YelmenEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Daniel John LawsonMedical Research Council Integrative Epidemiology Unit, Department of Population Health Sciences, Bristol Medical School, University of Bristol, United Kingdom.
Francesco MontinaroEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.
Luca PaganiEstonian Biocentre, Institute of Genomics, University of Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contemporary individuals are the combination of genetic fragments inherited from ancestors belonging to multiple populations, as the result of migration and admixture. Isolating and characterizing these layers are crucial to the understanding of the genetic history of a given population. Ancestry deconvolution approaches make use of a large amount of source individuals, therefore constraining the performance of Local Ancestry Inferences when only few genomes are available from a given population. Here we present WINC, a local ancestry framework derived from the combination of ChromoPainter and NNLS approaches, as a method to retrieve local genetic assignments when only a few reference individuals are available. The framework is aided by a score assignment based on source differentiation to maximize the amount of sequences retrieved and is capable of retrieving accurate ancestry assignments when only two individuals for source populations are used.

Indexed as

Chromosome PaintingGenomicsHumansInheritance PatternsLeast-Squares AnalysisSoftwareadmixtureChromoPainterlocal ancestryNNLS

Identifiers

PMID33585906
PMCPMC8085126

What OpenQuestion holds

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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.