IntroMap: a signal analysis based method for the detection of genomic introgressions

Abstract Background Breeding programs often rely on marker-assisted tests or variant calling of next generation sequence (NGS) data to identify regions of genomic introgression arising from the hybridization of two plant species. In this paper we present IntroMap, a bioinformatics pipeline for the s...

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Main Authors: Daniel J. Shea, Motoki Shimizu, Namiko Nishida, Eigo Fukai, Takashi Abe, Ryo Fujimoto, Keiichi Okazaki
Format: Article
Language:English
Published: BMC 2017-12-01
Series:BMC Genetics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12863-017-0568-5
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spelling doaj-c7983957c89a44a390af61b27e3200992020-11-25T03:17:13ZengBMCBMC Genetics1471-21562017-12-0118111210.1186/s12863-017-0568-5IntroMap: a signal analysis based method for the detection of genomic introgressionsDaniel J. Shea0Motoki Shimizu1Namiko Nishida2Eigo Fukai3Takashi Abe4Ryo Fujimoto5Keiichi Okazaki6Laboratory of Plant Breeding, Graduate School of Science and Technology, Niigata UniversityIwate Biotechnology Research CenterGraduate School of Agricultural Science, Kobe UniversityLaboratory of Plant Breeding, Graduate School of Science and Technology, Niigata UniversityDepartment of Computer Science, Graduate School of Science and Technology, Niigata UniversityGraduate School of Agricultural Science, Kobe UniversityLaboratory of Plant Breeding, Graduate School of Science and Technology, Niigata UniversityAbstract Background Breeding programs often rely on marker-assisted tests or variant calling of next generation sequence (NGS) data to identify regions of genomic introgression arising from the hybridization of two plant species. In this paper we present IntroMap, a bioinformatics pipeline for the screening of candidate plants through the application of signal processing techniques to NGS data, using alignment to a reference genome sequence (annotation is not required) that shares homology with the recurrent parental cultivar, and without the need for de novo assembly of the read data or variant calling. Results We show the accurate identification of introgressed genomic regions using both in silico simulated genomes, and a hybridized cultivar data set using our pipeline. Additionally we show, through targeted marker-based assays, validation of the IntroMap predicted regions for the hybrid cultivar. Conclusions This approach can be used to automate the screening of large populations, reducing the time and labor required, and can improve the accuracy of the detection of introgressed regions in comparison to a marker-based approach. In contrast to other approaches that generally rely upon a variant calling step, our method achieves accurate identification of introgressed regions without variant calling, relying solely upon alignment.http://link.springer.com/article/10.1186/s12863-017-0568-5Plant breedingInterspecific hybridizationIntrogressionSignal analysis
collection DOAJ
language English
format Article
sources DOAJ
author Daniel J. Shea
Motoki Shimizu
Namiko Nishida
Eigo Fukai
Takashi Abe
Ryo Fujimoto
Keiichi Okazaki
spellingShingle Daniel J. Shea
Motoki Shimizu
Namiko Nishida
Eigo Fukai
Takashi Abe
Ryo Fujimoto
Keiichi Okazaki
IntroMap: a signal analysis based method for the detection of genomic introgressions
BMC Genetics
Plant breeding
Interspecific hybridization
Introgression
Signal analysis
author_facet Daniel J. Shea
Motoki Shimizu
Namiko Nishida
Eigo Fukai
Takashi Abe
Ryo Fujimoto
Keiichi Okazaki
author_sort Daniel J. Shea
title IntroMap: a signal analysis based method for the detection of genomic introgressions
title_short IntroMap: a signal analysis based method for the detection of genomic introgressions
title_full IntroMap: a signal analysis based method for the detection of genomic introgressions
title_fullStr IntroMap: a signal analysis based method for the detection of genomic introgressions
title_full_unstemmed IntroMap: a signal analysis based method for the detection of genomic introgressions
title_sort intromap: a signal analysis based method for the detection of genomic introgressions
publisher BMC
series BMC Genetics
issn 1471-2156
publishDate 2017-12-01
description Abstract Background Breeding programs often rely on marker-assisted tests or variant calling of next generation sequence (NGS) data to identify regions of genomic introgression arising from the hybridization of two plant species. In this paper we present IntroMap, a bioinformatics pipeline for the screening of candidate plants through the application of signal processing techniques to NGS data, using alignment to a reference genome sequence (annotation is not required) that shares homology with the recurrent parental cultivar, and without the need for de novo assembly of the read data or variant calling. Results We show the accurate identification of introgressed genomic regions using both in silico simulated genomes, and a hybridized cultivar data set using our pipeline. Additionally we show, through targeted marker-based assays, validation of the IntroMap predicted regions for the hybrid cultivar. Conclusions This approach can be used to automate the screening of large populations, reducing the time and labor required, and can improve the accuracy of the detection of introgressed regions in comparison to a marker-based approach. In contrast to other approaches that generally rely upon a variant calling step, our method achieves accurate identification of introgressed regions without variant calling, relying solely upon alignment.
topic Plant breeding
Interspecific hybridization
Introgression
Signal analysis
url http://link.springer.com/article/10.1186/s12863-017-0568-5
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