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Targeted parallel sequencing of large genetically-defined genomic regions for identifying mutations in Arabidopsis.


ABSTRACT: Large-scale genetic screens in Arabidopsis are a powerful approach for molecular dissection of complex signaling networks. However, map-based cloning can be time-consuming or even hampered due to low chromosomal recombination. Current strategies using next generation sequencing for molecular identification of mutations require whole genome sequencing and advanced computational devises and skills, which are not readily accessible or affordable to every laboratory. We have developed a streamlined method using parallel massive sequencing for mutant identification in which only targeted regions are sequenced. This targeted parallel sequencing (TPSeq) method is more cost-effective, straightforward enough to be easily done without specialized bioinformatics expertise, and reliable for identifying multiple mutations simultaneously. Here, we demonstrate its use by identifying three novel nitrate-signaling mutants in Arabidopsis.

SUBMITTER: Liu KH 

PROVIDER: S-EPMC3348062 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

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Targeted parallel sequencing of large genetically-defined genomic regions for identifying mutations in Arabidopsis.

Liu Kun-Hsiang KH   McCormack Matthew M   Sheen Jen J  

Plant methods 20120330


Large-scale genetic screens in Arabidopsis are a powerful approach for molecular dissection of complex signaling networks. However, map-based cloning can be time-consuming or even hampered due to low chromosomal recombination. Current strategies using next generation sequencing for molecular identification of mutations require whole genome sequencing and advanced computational devises and skills, which are not readily accessible or affordable to every laboratory. We have developed a streamlined  ...[more]

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