Evidence map›Paper›PMID 41025923›Full record

ArticleBriefings in bioinformatics2025

OligoY pipeline for full Y chromosome painting.

Isabela Almeida, Henry A B Bruno, Eduardo Guimarães Dupim, Mara Maria L Santana Pinheiro, Antonio Bernardo Carvalho, Maria D Vibranovski

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

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5 · Who and what money

Authors and funding

6 authors.

Isabela AlmeidaDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, 05508-090 SP, Brazil.ORCID 0000-0001-9995-782X
Henry A B BrunoDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, 05508-090 SP, Brazil.ORCID 0000-0002-0595-2671
Eduardo Guimarães DupimDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, 05508-090 SP, Brazil.ORCID 0000-0003-2540-7184
Mara Maria L Santana PinheiroDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, 05508-090 SP, Brazil.ORCID 0000-0002-6417-0637
Antonio Bernardo CarvalhoDepartment of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-902 RJ, Brazil.ORCID 0000-0001-8959-6469
Maria D VibranovskiDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, 05508-090 SP, Brazil.ORCID 0000-0001-8313-9726

Funding

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro CNE2018Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/08028-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/20844-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/10559-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/14878-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/13517-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/14607-6Wellcome TrustWellcome Trust 207486/Z/17/Z
6 · The paper itself

Abstract

The Y chromosome's unique structure poses challenges for cytogenetic studies, especially in designing probes for FISH Oligopaint labeling experiments (Fluorescence in situ hybridization). The standard protocol for designing probes for these experiments discards repetitive sequences to avoid off-target hybridization. Given the highly repetitive nature of the Y chromosome, assemblies often remain fragmented, leaving significant regions incompletely sequenced, unprobed, and poorly understood. Among these, the remaining nonrepetitive sequences are usually insufficient to design probes and efficiently perform FISH Oligopaint assays, since they do not cover most regions of the chromosome. This limitation hinders comprehensive cytogenetic studies, which are crucial not only for understanding the Y chromosome's role in genetics but also for broader applications in evolutionary biology, medicine, and conservation. Here, we introduce a new computational pipeline to design full chromosome fluorescent labeling probes for the Y chromosome of any species of interest. Based on open-source tools, the OligoY pipeline increases the amount of contigs assigned to the Y chromosome from the reference genome assembly, and effectively uses repetitive sequences unique to the target chromosome to design probes. Throughout its steps, the pipeline gives the user the autonomy to choose parameters, maximizing the overall efficiency of cytogenetic experiments. After extensive in silico and in situ testing and validation with the human and Drosophila melanogaster genomes, we show for the first time a pipeline for FISH Oligopaint probe design that significantly increases previous Y chromosome staining with no off-target signal.

Indexed as

Chromosome PaintingChromosomes, Human, YIn Situ Hybridization, FluorescenceSoftwareY ChromosomeAnimalsHumansMalecytogeneticsFISH OligopaintheterochromatinY chromosome

Identifiers

PMID41025923
PMCPMC12481694

What Socratic 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 Socratic graph.