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Decoding cell lineage from acquired mutations using arbitrary deep sequencing
Because mutations are inevitable, the genome of each cell in a multicellular organism becomes unique and therefore encodes a record of its ancestry. Here we couple arbitrary single primer PCR with “next generation” DNA sequencing in order to catalog mutations and deconvolve the phylogeny of cultured...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248619/ https://www.ncbi.nlm.nih.gov/pubmed/22120468 http://dx.doi.org/10.1038/nmeth.1781 |
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author | Carlson, Cheryl A Kas, Arnold Kirkwood, Robert Hays, Laura E Preston, Bradley D Salipante, Stephen J Horwitz, Marshall S |
author_facet | Carlson, Cheryl A Kas, Arnold Kirkwood, Robert Hays, Laura E Preston, Bradley D Salipante, Stephen J Horwitz, Marshall S |
author_sort | Carlson, Cheryl A |
collection | PubMed |
description | Because mutations are inevitable, the genome of each cell in a multicellular organism becomes unique and therefore encodes a record of its ancestry. Here we couple arbitrary single primer PCR with “next generation” DNA sequencing in order to catalog mutations and deconvolve the phylogeny of cultured mouse cells. This study helps pave the way toward construction of retrospective cell fate maps based on mutations accumulating in genomes of somatic cells. |
format | Online Article Text |
id | pubmed-3248619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-32486192012-07-01 Decoding cell lineage from acquired mutations using arbitrary deep sequencing Carlson, Cheryl A Kas, Arnold Kirkwood, Robert Hays, Laura E Preston, Bradley D Salipante, Stephen J Horwitz, Marshall S Nat Methods Article Because mutations are inevitable, the genome of each cell in a multicellular organism becomes unique and therefore encodes a record of its ancestry. Here we couple arbitrary single primer PCR with “next generation” DNA sequencing in order to catalog mutations and deconvolve the phylogeny of cultured mouse cells. This study helps pave the way toward construction of retrospective cell fate maps based on mutations accumulating in genomes of somatic cells. 2011-11-27 /pmc/articles/PMC3248619/ /pubmed/22120468 http://dx.doi.org/10.1038/nmeth.1781 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Carlson, Cheryl A Kas, Arnold Kirkwood, Robert Hays, Laura E Preston, Bradley D Salipante, Stephen J Horwitz, Marshall S Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title | Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title_full | Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title_fullStr | Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title_full_unstemmed | Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title_short | Decoding cell lineage from acquired mutations using arbitrary deep sequencing |
title_sort | decoding cell lineage from acquired mutations using arbitrary deep sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248619/ https://www.ncbi.nlm.nih.gov/pubmed/22120468 http://dx.doi.org/10.1038/nmeth.1781 |
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