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Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results
Present-day publications on human genes primarily feature genes that already appeared in many publications prior to completion of the Human Genome Project in 2003. These patterns persist despite the subsequent adoption of high-throughput technologies, which routinely identify novel genes associated...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002660/ https://www.ncbi.nlm.nih.gov/pubmed/36909550 http://dx.doi.org/10.1101/2023.02.28.530483 |
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author | Richardson, Reese AK Navarro, Heliodoro Tejedor Nunes Amaral, Luis A Stoeger, Thomas |
author_facet | Richardson, Reese AK Navarro, Heliodoro Tejedor Nunes Amaral, Luis A Stoeger, Thomas |
author_sort | Richardson, Reese AK |
collection | PubMed |
description | Present-day publications on human genes primarily feature genes that already appeared in many publications prior to completion of the Human Genome Project in 2003. These patterns persist despite the subsequent adoption of high-throughput technologies, which routinely identify novel genes associated with biological processes and disease. Although several hypotheses for bias in the selection of genes as research targets have been proposed, their explanatory powers have not yet been compared. Our analysis suggests that understudied genes are systematically abandoned in favor of better-studied genes between the completion of -omics experiments and the reporting of results. Understudied genes are similarly abandoned by studies that cite these -omics experiments. Conversely, we find that publications on understudied genes may even accrue a greater number of citations. Among 45 biological and experimental factors previously proposed to affect which genes are being studied, we find that 35 are significantly associated with the choice of hit genes presented in titles and abstracts of -omics studies. To promote the investigation of understudied genes we condense our insights into a tool, find my understudied genes (FMUG), that allows scientists to engage with potential bias during the selection of hits. We demonstrate the utility of FMUG through the identification of genes that remain understudied in vertebrate aging. FMUG is developed in Flutter and is available for download at fmug.amaral.northwestern.edu as a MacOS/Windows app. |
format | Online Article Text |
id | pubmed-10002660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100026602023-03-11 Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results Richardson, Reese AK Navarro, Heliodoro Tejedor Nunes Amaral, Luis A Stoeger, Thomas bioRxiv Article Present-day publications on human genes primarily feature genes that already appeared in many publications prior to completion of the Human Genome Project in 2003. These patterns persist despite the subsequent adoption of high-throughput technologies, which routinely identify novel genes associated with biological processes and disease. Although several hypotheses for bias in the selection of genes as research targets have been proposed, their explanatory powers have not yet been compared. Our analysis suggests that understudied genes are systematically abandoned in favor of better-studied genes between the completion of -omics experiments and the reporting of results. Understudied genes are similarly abandoned by studies that cite these -omics experiments. Conversely, we find that publications on understudied genes may even accrue a greater number of citations. Among 45 biological and experimental factors previously proposed to affect which genes are being studied, we find that 35 are significantly associated with the choice of hit genes presented in titles and abstracts of -omics studies. To promote the investigation of understudied genes we condense our insights into a tool, find my understudied genes (FMUG), that allows scientists to engage with potential bias during the selection of hits. We demonstrate the utility of FMUG through the identification of genes that remain understudied in vertebrate aging. FMUG is developed in Flutter and is available for download at fmug.amaral.northwestern.edu as a MacOS/Windows app. Cold Spring Harbor Laboratory 2023-10-31 /pmc/articles/PMC10002660/ /pubmed/36909550 http://dx.doi.org/10.1101/2023.02.28.530483 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Richardson, Reese AK Navarro, Heliodoro Tejedor Nunes Amaral, Luis A Stoeger, Thomas Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title | Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title_full | Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title_fullStr | Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title_full_unstemmed | Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title_short | Meta-Research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
title_sort | meta-research: understudied genes are lost in a leaky pipeline between genome-wide assays and reporting of results |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002660/ https://www.ncbi.nlm.nih.gov/pubmed/36909550 http://dx.doi.org/10.1101/2023.02.28.530483 |
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