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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...

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Autores principales: Carlson, Cheryl A, Kas, Arnold, Kirkwood, Robert, Hays, Laura E, Preston, Bradley D, Salipante, Stephen J, Horwitz, Marshall S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
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.
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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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