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DSMNC: a database of somatic mutations in normal cells
Numerous non-inherited somatic mutations, distinct from those of germ-line origin, occur in somatic cells during DNA replication per cell-division. The somatic mutations, recording the unique genetic cell-lineage ‘history’ of each proliferating normal cell, are important but remain to be investigate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323907/ https://www.ncbi.nlm.nih.gov/pubmed/30380071 http://dx.doi.org/10.1093/nar/gky1045 |
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author | Miao, Xuexia Li, Xi Wang, Lifei Zheng, Caihong Cai, Jun |
author_facet | Miao, Xuexia Li, Xi Wang, Lifei Zheng, Caihong Cai, Jun |
author_sort | Miao, Xuexia |
collection | PubMed |
description | Numerous non-inherited somatic mutations, distinct from those of germ-line origin, occur in somatic cells during DNA replication per cell-division. The somatic mutations, recording the unique genetic cell-lineage ‘history’ of each proliferating normal cell, are important but remain to be investigated because of their ultra-low frequency hidden in the genetic background of heterogeneous cells. Luckily, the recent development of single-cell genomics biotechnologies enables the screening and collection of the somatic mutations, especial single nucleotide variations (SNVs), occurring in normal cells. Here, we established DSMNC: a database of somatic mutations in normal cells (http://dsmnc.big.ac.cn/), which provides most comprehensive catalogue of somatic SNVs in single cells from various normal tissues. In the current version, the database collected ∼0.8 million SNVs accumulated in ∼600 single normal cells (579 human cells and 39 mouse cells). The database interface supports the user-friendly capability of browsing and searching the SNVs and their annotation information. DSMNC, which serves as a timely and valuable collection of somatic mutations in individual normal cells, has made it possible to analyze the burdens and signatures of somatic mutations in various types of heterogeneous normal cells. Therefore, DSMNC will significantly improve our understanding of the characteristics of somatic mutations in normal cells. |
format | Online Article Text |
id | pubmed-6323907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63239072019-01-10 DSMNC: a database of somatic mutations in normal cells Miao, Xuexia Li, Xi Wang, Lifei Zheng, Caihong Cai, Jun Nucleic Acids Res Database Issue Numerous non-inherited somatic mutations, distinct from those of germ-line origin, occur in somatic cells during DNA replication per cell-division. The somatic mutations, recording the unique genetic cell-lineage ‘history’ of each proliferating normal cell, are important but remain to be investigated because of their ultra-low frequency hidden in the genetic background of heterogeneous cells. Luckily, the recent development of single-cell genomics biotechnologies enables the screening and collection of the somatic mutations, especial single nucleotide variations (SNVs), occurring in normal cells. Here, we established DSMNC: a database of somatic mutations in normal cells (http://dsmnc.big.ac.cn/), which provides most comprehensive catalogue of somatic SNVs in single cells from various normal tissues. In the current version, the database collected ∼0.8 million SNVs accumulated in ∼600 single normal cells (579 human cells and 39 mouse cells). The database interface supports the user-friendly capability of browsing and searching the SNVs and their annotation information. DSMNC, which serves as a timely and valuable collection of somatic mutations in individual normal cells, has made it possible to analyze the burdens and signatures of somatic mutations in various types of heterogeneous normal cells. Therefore, DSMNC will significantly improve our understanding of the characteristics of somatic mutations in normal cells. Oxford University Press 2019-01-08 2018-10-31 /pmc/articles/PMC6323907/ /pubmed/30380071 http://dx.doi.org/10.1093/nar/gky1045 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Miao, Xuexia Li, Xi Wang, Lifei Zheng, Caihong Cai, Jun DSMNC: a database of somatic mutations in normal cells |
title | DSMNC: a database of somatic mutations in normal cells |
title_full | DSMNC: a database of somatic mutations in normal cells |
title_fullStr | DSMNC: a database of somatic mutations in normal cells |
title_full_unstemmed | DSMNC: a database of somatic mutations in normal cells |
title_short | DSMNC: a database of somatic mutations in normal cells |
title_sort | dsmnc: a database of somatic mutations in normal cells |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323907/ https://www.ncbi.nlm.nih.gov/pubmed/30380071 http://dx.doi.org/10.1093/nar/gky1045 |
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