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Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly
BACKGROUND: De novo reference assemblies that are affordable, practical to produce, and of sufficient quality for most downstream applications, remain an unattained goal for many taxa. Insects, which may yield too little DNA from individual specimens for long-read sequencing library construction and...
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/PMC4779211/ https://www.ncbi.nlm.nih.gov/pubmed/26944054 http://dx.doi.org/10.1186/s12864-016-2531-7 |
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author | Love, R. Rebecca Weisenfeld, Neil I. Jaffe, David B. Besansky, Nora J. Neafsey, Daniel E. |
author_facet | Love, R. Rebecca Weisenfeld, Neil I. Jaffe, David B. Besansky, Nora J. Neafsey, Daniel E. |
author_sort | Love, R. Rebecca |
collection | PubMed |
description | BACKGROUND: De novo reference assemblies that are affordable, practical to produce, and of sufficient quality for most downstream applications, remain an unattained goal for many taxa. Insects, which may yield too little DNA from individual specimens for long-read sequencing library construction and often have highly heterozygous genomes, can be particularly hard to assemble using inexpensive short-read sequencing data. The large number of insect species with medical or economic importance makes this a critical problem to address. RESULTS: Using the assembler DISCOVAR de novo, we assembled the genome of the African malaria mosquito Anopheles arabiensis using 250 bp reads from a single library. The resulting assembly had a contig N50 of 22,433 bp, and recovered the gene set nearly as well as the ALLPATHS-LG AaraD1 An. arabiensis assembly produced with reads from three sequencing libraries and much greater resources. DISCOVAR de novo appeared to perform better than ALLPATHS-LG in regions of low complexity. CONCLUSIONS: DISCOVAR de novo performed well assembling the genome of an insect of medical importance, using simpler sequencing input than previous anopheline assemblies. We have shown that this program is a viable tool for cost-effective assembly of a modestly-sized insect genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2531-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4779211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47792112016-03-06 Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly Love, R. Rebecca Weisenfeld, Neil I. Jaffe, David B. Besansky, Nora J. Neafsey, Daniel E. BMC Genomics Research Article BACKGROUND: De novo reference assemblies that are affordable, practical to produce, and of sufficient quality for most downstream applications, remain an unattained goal for many taxa. Insects, which may yield too little DNA from individual specimens for long-read sequencing library construction and often have highly heterozygous genomes, can be particularly hard to assemble using inexpensive short-read sequencing data. The large number of insect species with medical or economic importance makes this a critical problem to address. RESULTS: Using the assembler DISCOVAR de novo, we assembled the genome of the African malaria mosquito Anopheles arabiensis using 250 bp reads from a single library. The resulting assembly had a contig N50 of 22,433 bp, and recovered the gene set nearly as well as the ALLPATHS-LG AaraD1 An. arabiensis assembly produced with reads from three sequencing libraries and much greater resources. DISCOVAR de novo appeared to perform better than ALLPATHS-LG in regions of low complexity. CONCLUSIONS: DISCOVAR de novo performed well assembling the genome of an insect of medical importance, using simpler sequencing input than previous anopheline assemblies. We have shown that this program is a viable tool for cost-effective assembly of a modestly-sized insect genome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2531-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-05 /pmc/articles/PMC4779211/ /pubmed/26944054 http://dx.doi.org/10.1186/s12864-016-2531-7 Text en © Love 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 | Research Article Love, R. Rebecca Weisenfeld, Neil I. Jaffe, David B. Besansky, Nora J. Neafsey, Daniel E. Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title | Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title_full | Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title_fullStr | Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title_full_unstemmed | Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title_short | Evaluation of DISCOVAR de novo using a mosquito sample for cost-effective short-read genome assembly |
title_sort | evaluation of discovar de novo using a mosquito sample for cost-effective short-read genome assembly |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779211/ https://www.ncbi.nlm.nih.gov/pubmed/26944054 http://dx.doi.org/10.1186/s12864-016-2531-7 |
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