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Chromosome-scale shotgun assembly using an in vitro method for long-range linkage
Long-range and highly accurate de novo assembly from short-read data is one of the most pressing challenges in genomics. Recently, it has been shown that read pairs generated by proximity ligation of DNA in chromatin of living tissue can address this problem, dramatically increasing the scaffold con...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772016/ https://www.ncbi.nlm.nih.gov/pubmed/26848124 http://dx.doi.org/10.1101/gr.193474.115 |
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author | Putnam, Nicholas H. O'Connell, Brendan L. Stites, Jonathan C. Rice, Brandon J. Blanchette, Marco Calef, Robert Troll, Christopher J. Fields, Andrew Hartley, Paul D. Sugnet, Charles W. Haussler, David Rokhsar, Daniel S. Green, Richard E. |
author_facet | Putnam, Nicholas H. O'Connell, Brendan L. Stites, Jonathan C. Rice, Brandon J. Blanchette, Marco Calef, Robert Troll, Christopher J. Fields, Andrew Hartley, Paul D. Sugnet, Charles W. Haussler, David Rokhsar, Daniel S. Green, Richard E. |
author_sort | Putnam, Nicholas H. |
collection | PubMed |
description | Long-range and highly accurate de novo assembly from short-read data is one of the most pressing challenges in genomics. Recently, it has been shown that read pairs generated by proximity ligation of DNA in chromatin of living tissue can address this problem, dramatically increasing the scaffold contiguity of assemblies. Here, we describe a simpler approach (“Chicago”) based on in vitro reconstituted chromatin. We generated two Chicago data sets with human DNA and developed a statistical model and a new software pipeline (“HiRise”) that can identify poor quality joins and produce accurate, long-range sequence scaffolds. We used these to construct a highly accurate de novo assembly and scaffolding of a human genome with scaffold N50 of 20 Mbp. We also demonstrated the utility of Chicago for improving existing assemblies by reassembling and scaffolding the genome of the American alligator. With a single library and one lane of Illumina HiSeq sequencing, we increased the scaffold N50 of the American alligator from 508 kbp to 10 Mbp. |
format | Online Article Text |
id | pubmed-4772016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47720162016-03-15 Chromosome-scale shotgun assembly using an in vitro method for long-range linkage Putnam, Nicholas H. O'Connell, Brendan L. Stites, Jonathan C. Rice, Brandon J. Blanchette, Marco Calef, Robert Troll, Christopher J. Fields, Andrew Hartley, Paul D. Sugnet, Charles W. Haussler, David Rokhsar, Daniel S. Green, Richard E. Genome Res Method Long-range and highly accurate de novo assembly from short-read data is one of the most pressing challenges in genomics. Recently, it has been shown that read pairs generated by proximity ligation of DNA in chromatin of living tissue can address this problem, dramatically increasing the scaffold contiguity of assemblies. Here, we describe a simpler approach (“Chicago”) based on in vitro reconstituted chromatin. We generated two Chicago data sets with human DNA and developed a statistical model and a new software pipeline (“HiRise”) that can identify poor quality joins and produce accurate, long-range sequence scaffolds. We used these to construct a highly accurate de novo assembly and scaffolding of a human genome with scaffold N50 of 20 Mbp. We also demonstrated the utility of Chicago for improving existing assemblies by reassembling and scaffolding the genome of the American alligator. With a single library and one lane of Illumina HiSeq sequencing, we increased the scaffold N50 of the American alligator from 508 kbp to 10 Mbp. Cold Spring Harbor Laboratory Press 2016-03 /pmc/articles/PMC4772016/ /pubmed/26848124 http://dx.doi.org/10.1101/gr.193474.115 Text en © 2016 Putnam et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Method Putnam, Nicholas H. O'Connell, Brendan L. Stites, Jonathan C. Rice, Brandon J. Blanchette, Marco Calef, Robert Troll, Christopher J. Fields, Andrew Hartley, Paul D. Sugnet, Charles W. Haussler, David Rokhsar, Daniel S. Green, Richard E. Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title | Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title_full | Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title_fullStr | Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title_full_unstemmed | Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title_short | Chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
title_sort | chromosome-scale shotgun assembly using an in vitro method for long-range linkage |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772016/ https://www.ncbi.nlm.nih.gov/pubmed/26848124 http://dx.doi.org/10.1101/gr.193474.115 |
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