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A Biomedically Enriched Collection of 7000 Human ORF Clones
We report the production and availability of over 7000 fully sequence verified plasmid ORF clones representing over 3400 unique human genes. These ORF clones were derived using the human MGC collection as template and were produced in two formats: with and without stop codons. Thus, this collection...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211400/ https://www.ncbi.nlm.nih.gov/pubmed/18231609 http://dx.doi.org/10.1371/journal.pone.0001528 |
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author | Rolfs, Andreas Hu, Yanhui Ebert, Lars Hoffmann, Dietmar Zuo, Dongmei Ramachandran, Niro Raphael, Jacob Kelley, Fontina McCarron, Seamus Jepson, Daniel A. Shen, Binghua Baqui, Munira M. A. Pearlberg, Joseph Taycher, Elena DeLoughery, Craig Hoerlein, Andreas Korn, Bernhard LaBaer, Joshua |
author_facet | Rolfs, Andreas Hu, Yanhui Ebert, Lars Hoffmann, Dietmar Zuo, Dongmei Ramachandran, Niro Raphael, Jacob Kelley, Fontina McCarron, Seamus Jepson, Daniel A. Shen, Binghua Baqui, Munira M. A. Pearlberg, Joseph Taycher, Elena DeLoughery, Craig Hoerlein, Andreas Korn, Bernhard LaBaer, Joshua |
author_sort | Rolfs, Andreas |
collection | PubMed |
description | We report the production and availability of over 7000 fully sequence verified plasmid ORF clones representing over 3400 unique human genes. These ORF clones were derived using the human MGC collection as template and were produced in two formats: with and without stop codons. Thus, this collection supports the production of either native protein or proteins with fusion tags added to either or both ends. The template clones used to generate this collection were enriched in three ways. First, gene redundancy was removed. Second, clones were selected to represent the best available GenBank reference sequence. Finally, a literature-based software tool was used to evaluate the list of target genes to ensure that it broadly reflected biomedical research interests. The target gene list was compared with 4000 human diseases and over 8500 biological and chemical MeSH classes in ∼15 Million publications recorded in PubMed at the time of analysis. The outcome of this analysis revealed that relative to the genome and the MGC collection, this collection is enriched for the presence of genes with published associations with a wide range of diseases and biomedical terms without displaying a particular bias towards any single disease or concept. Thus, this collection is likely to be a powerful resource for researchers who wish to study protein function in a set of genes with documented biomedical significance. |
format | Text |
id | pubmed-2211400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22114002008-01-30 A Biomedically Enriched Collection of 7000 Human ORF Clones Rolfs, Andreas Hu, Yanhui Ebert, Lars Hoffmann, Dietmar Zuo, Dongmei Ramachandran, Niro Raphael, Jacob Kelley, Fontina McCarron, Seamus Jepson, Daniel A. Shen, Binghua Baqui, Munira M. A. Pearlberg, Joseph Taycher, Elena DeLoughery, Craig Hoerlein, Andreas Korn, Bernhard LaBaer, Joshua PLoS One Research Article We report the production and availability of over 7000 fully sequence verified plasmid ORF clones representing over 3400 unique human genes. These ORF clones were derived using the human MGC collection as template and were produced in two formats: with and without stop codons. Thus, this collection supports the production of either native protein or proteins with fusion tags added to either or both ends. The template clones used to generate this collection were enriched in three ways. First, gene redundancy was removed. Second, clones were selected to represent the best available GenBank reference sequence. Finally, a literature-based software tool was used to evaluate the list of target genes to ensure that it broadly reflected biomedical research interests. The target gene list was compared with 4000 human diseases and over 8500 biological and chemical MeSH classes in ∼15 Million publications recorded in PubMed at the time of analysis. The outcome of this analysis revealed that relative to the genome and the MGC collection, this collection is enriched for the presence of genes with published associations with a wide range of diseases and biomedical terms without displaying a particular bias towards any single disease or concept. Thus, this collection is likely to be a powerful resource for researchers who wish to study protein function in a set of genes with documented biomedical significance. Public Library of Science 2008-01-30 /pmc/articles/PMC2211400/ /pubmed/18231609 http://dx.doi.org/10.1371/journal.pone.0001528 Text en Rolfs et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rolfs, Andreas Hu, Yanhui Ebert, Lars Hoffmann, Dietmar Zuo, Dongmei Ramachandran, Niro Raphael, Jacob Kelley, Fontina McCarron, Seamus Jepson, Daniel A. Shen, Binghua Baqui, Munira M. A. Pearlberg, Joseph Taycher, Elena DeLoughery, Craig Hoerlein, Andreas Korn, Bernhard LaBaer, Joshua A Biomedically Enriched Collection of 7000 Human ORF Clones |
title | A Biomedically Enriched Collection of 7000 Human ORF Clones |
title_full | A Biomedically Enriched Collection of 7000 Human ORF Clones |
title_fullStr | A Biomedically Enriched Collection of 7000 Human ORF Clones |
title_full_unstemmed | A Biomedically Enriched Collection of 7000 Human ORF Clones |
title_short | A Biomedically Enriched Collection of 7000 Human ORF Clones |
title_sort | biomedically enriched collection of 7000 human orf clones |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211400/ https://www.ncbi.nlm.nih.gov/pubmed/18231609 http://dx.doi.org/10.1371/journal.pone.0001528 |
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