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The status of the human gene catalogue

Scientists have been trying to identify all of the genes in the human genome since the initial draft of the genome was published in 2001. Over the intervening years, much progress has been made in identifying protein-coding genes, and the estimated number has shrunk to fewer than 20,000, although th...

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Autores principales: Amaral, Paulo, Carbonell-Sala, Silvia, De La Vega, Francisco M., Faial, Tiago, Frankish, Adam, Gingeras, Thomas, Guigo, Roderic, Harrow, Jennifer L, Hatzigeorgiou, Artemis G., Johnson, Rory, Murphy, Terence D., Pertea, Mihaela, Pruitt, Kim D., Pujar, Shashikant, Takahashi, Hazuki, Ulitsky, Igor, Varabyou, Ales, Wells, Christine A., Yandell, Mark, Carninci, Piero, Salzberg, Steven L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornell University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055485/
https://www.ncbi.nlm.nih.gov/pubmed/36994150
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author Amaral, Paulo
Carbonell-Sala, Silvia
De La Vega, Francisco M.
Faial, Tiago
Frankish, Adam
Gingeras, Thomas
Guigo, Roderic
Harrow, Jennifer L
Hatzigeorgiou, Artemis G.
Johnson, Rory
Murphy, Terence D.
Pertea, Mihaela
Pruitt, Kim D.
Pujar, Shashikant
Takahashi, Hazuki
Ulitsky, Igor
Varabyou, Ales
Wells, Christine A.
Yandell, Mark
Carninci, Piero
Salzberg, Steven L.
author_facet Amaral, Paulo
Carbonell-Sala, Silvia
De La Vega, Francisco M.
Faial, Tiago
Frankish, Adam
Gingeras, Thomas
Guigo, Roderic
Harrow, Jennifer L
Hatzigeorgiou, Artemis G.
Johnson, Rory
Murphy, Terence D.
Pertea, Mihaela
Pruitt, Kim D.
Pujar, Shashikant
Takahashi, Hazuki
Ulitsky, Igor
Varabyou, Ales
Wells, Christine A.
Yandell, Mark
Carninci, Piero
Salzberg, Steven L.
author_sort Amaral, Paulo
collection PubMed
description Scientists have been trying to identify all of the genes in the human genome since the initial draft of the genome was published in 2001. Over the intervening years, much progress has been made in identifying protein-coding genes, and the estimated number has shrunk to fewer than 20,000, although the number of distinct protein-coding isoforms has expanded dramatically. The invention of high-throughput RNA sequencing and other technological breakthroughs have led to an explosion in the number of reported non-coding RNA genes, although most of them do not yet have any known function. A combination of recent advances offers a path forward to identifying these functions and towards eventually completing the human gene catalogue. However, much work remains to be done before we have a universal annotation standard that includes all medically significant genes, maintains their relationships with different reference genomes, and describes clinically relevant genetic variants.
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spelling pubmed-100554852023-03-30 The status of the human gene catalogue Amaral, Paulo Carbonell-Sala, Silvia De La Vega, Francisco M. Faial, Tiago Frankish, Adam Gingeras, Thomas Guigo, Roderic Harrow, Jennifer L Hatzigeorgiou, Artemis G. Johnson, Rory Murphy, Terence D. Pertea, Mihaela Pruitt, Kim D. Pujar, Shashikant Takahashi, Hazuki Ulitsky, Igor Varabyou, Ales Wells, Christine A. Yandell, Mark Carninci, Piero Salzberg, Steven L. ArXiv Article Scientists have been trying to identify all of the genes in the human genome since the initial draft of the genome was published in 2001. Over the intervening years, much progress has been made in identifying protein-coding genes, and the estimated number has shrunk to fewer than 20,000, although the number of distinct protein-coding isoforms has expanded dramatically. The invention of high-throughput RNA sequencing and other technological breakthroughs have led to an explosion in the number of reported non-coding RNA genes, although most of them do not yet have any known function. A combination of recent advances offers a path forward to identifying these functions and towards eventually completing the human gene catalogue. However, much work remains to be done before we have a universal annotation standard that includes all medically significant genes, maintains their relationships with different reference genomes, and describes clinically relevant genetic variants. Cornell University 2023-03-24 /pmc/articles/PMC10055485/ /pubmed/36994150 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Amaral, Paulo
Carbonell-Sala, Silvia
De La Vega, Francisco M.
Faial, Tiago
Frankish, Adam
Gingeras, Thomas
Guigo, Roderic
Harrow, Jennifer L
Hatzigeorgiou, Artemis G.
Johnson, Rory
Murphy, Terence D.
Pertea, Mihaela
Pruitt, Kim D.
Pujar, Shashikant
Takahashi, Hazuki
Ulitsky, Igor
Varabyou, Ales
Wells, Christine A.
Yandell, Mark
Carninci, Piero
Salzberg, Steven L.
The status of the human gene catalogue
title The status of the human gene catalogue
title_full The status of the human gene catalogue
title_fullStr The status of the human gene catalogue
title_full_unstemmed The status of the human gene catalogue
title_short The status of the human gene catalogue
title_sort status of the human gene catalogue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055485/
https://www.ncbi.nlm.nih.gov/pubmed/36994150
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