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Identifying crossover locations in an Arabidopsis thaliana Ler x Col/Ler backcross F1 population using genotyping by sequencing for male-specific crossover map

ABSTRACT: Identifying crossover locations in an Arabidopsis thaliana Ler x Col/Ler backcross F1 population using genotyping by sequencing for male-specific crossover map

PROVIDER: PRJEB60397 | ENA |

REPOSITORIES: ENA

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Dataset's files

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			Action	DRS
	ERR10960400_1.fastq.gz	Fastqsanger.gz
	ERR10960400_2.fastq.gz	Fastqsanger.gz
	ERR10960401_1.fastq.gz	Fastqsanger.gz
	ERR10960401_2.fastq.gz	Fastqsanger.gz
	ERR10960402_1.fastq.gz	Fastqsanger.gz

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Identifying crossover locations in an Arabidopsis thaliana Col/Ler x Ler backcross F1 population using genotyping by sequencing for female-specific crossover map

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Identifying crossover locations in an Arabidopsis thaliana Ler x Col/Ler backcross F1 population using genotyping by sequencing for male-specific crossover map

Project description:Genomic DNA from 96 Ler x Col/Ler backcross F1 population was extracted using CTAB and used to generate sequencing libraries as described (Rowan et al; Yelina et al), with the following modifications. DNA was extracted from 3 rosette leaves of 5 week old plants and 150 ng of DNA used as input for each library. DNA shearing was carried out for 20 minutes at 37°C with 0.4U of DNA Shearase (Zymo research). The barcoded adapters used for library construction are listed in Rowan et al. Each set of 96 libraries was sequenced on one lane of an Illumina NextSeq500 instrument (300-cycle Mid Output run). Sequencing data was analysed to identify crossovers as previously reported, using the TIGER pipeline.

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Project description:Genomic DNA from 96 Col/Ler x Ler backcross F1 population was extracted using CTAB and used to generate sequencing libraries as described (Rowan et al; Yelina et al), with the following modifications. DNA was extracted from 3 rosette leaves of 5 week old plants and 150 ng of DNA used as input for each library. DNA shearing was carried out for 20 minutes at 37°C with 0.4U of DNA Shearase (Zymo research). The barcoded adapters used for library construction are listed in Rowan et al. Each set of 96 libraries was sequenced on one lane of an Illumina NextSeq500 instrument (300-cycle Mid Output run). Sequencing data was analysed to identify crossovers as previously reported, using the TIGER pipeline.

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