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Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies
BACKGROUND: The cell line BT-474 is a popular cell line for studying the biology of cancer and developing novel drugs. However, there is no complete, published genome sequence for this highly utilized scientific resource. In this study we sought to provide a comprehensive and useful data set for the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748558/ https://www.ncbi.nlm.nih.gov/pubmed/26865974 http://dx.doi.org/10.1186/s13742-016-0113-x |
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author | Ciotlos, Serban Mao, Qing Zhang, Rebecca Yu Li, Zhenyu Chin, Robert Gulbahce, Natali Liu, Sophie Jia Drmanac, Radoje Peters, Brock A. |
author_facet | Ciotlos, Serban Mao, Qing Zhang, Rebecca Yu Li, Zhenyu Chin, Robert Gulbahce, Natali Liu, Sophie Jia Drmanac, Radoje Peters, Brock A. |
author_sort | Ciotlos, Serban |
collection | PubMed |
description | BACKGROUND: The cell line BT-474 is a popular cell line for studying the biology of cancer and developing novel drugs. However, there is no complete, published genome sequence for this highly utilized scientific resource. In this study we sought to provide a comprehensive and useful data set for the scientific community by generating a whole genome sequence for BT-474. FINDINGS: Five μg of genomic DNA, isolated from an early passage of the BT-474 cell line, was used to generate a whole genome sequence (114X coverage) using Complete Genomics’ standard sequencing process. To provide additional variant phasing and structural variation data we also processed and analyzed two separate libraries of 5 and 6 individual cells to depths of 99X and 87X, respectively, using Complete Genomics’ Long Fragment Read (LFR) technology. CONCLUSIONS: BT-474 is a highly aneuploid cell line with an extremely complex genome sequence. This ~300X total coverage genome sequence provides a more complete understanding of this highly utilized cell line at the genomic level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13742-016-0113-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4748558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47485582016-02-11 Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies Ciotlos, Serban Mao, Qing Zhang, Rebecca Yu Li, Zhenyu Chin, Robert Gulbahce, Natali Liu, Sophie Jia Drmanac, Radoje Peters, Brock A. Gigascience Data Note BACKGROUND: The cell line BT-474 is a popular cell line for studying the biology of cancer and developing novel drugs. However, there is no complete, published genome sequence for this highly utilized scientific resource. In this study we sought to provide a comprehensive and useful data set for the scientific community by generating a whole genome sequence for BT-474. FINDINGS: Five μg of genomic DNA, isolated from an early passage of the BT-474 cell line, was used to generate a whole genome sequence (114X coverage) using Complete Genomics’ standard sequencing process. To provide additional variant phasing and structural variation data we also processed and analyzed two separate libraries of 5 and 6 individual cells to depths of 99X and 87X, respectively, using Complete Genomics’ Long Fragment Read (LFR) technology. CONCLUSIONS: BT-474 is a highly aneuploid cell line with an extremely complex genome sequence. This ~300X total coverage genome sequence provides a more complete understanding of this highly utilized cell line at the genomic level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13742-016-0113-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-09 /pmc/articles/PMC4748558/ /pubmed/26865974 http://dx.doi.org/10.1186/s13742-016-0113-x Text en © Ciotlos et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Data Note Ciotlos, Serban Mao, Qing Zhang, Rebecca Yu Li, Zhenyu Chin, Robert Gulbahce, Natali Liu, Sophie Jia Drmanac, Radoje Peters, Brock A. Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title | Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title_full | Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title_fullStr | Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title_full_unstemmed | Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title_short | Whole genome sequence analysis of BT-474 using complete Genomics’ standard and long fragment read technologies |
title_sort | whole genome sequence analysis of bt-474 using complete genomics’ standard and long fragment read technologies |
topic | Data Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748558/ https://www.ncbi.nlm.nih.gov/pubmed/26865974 http://dx.doi.org/10.1186/s13742-016-0113-x |
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