Caenorhabditis elegans mutant allele identification by whole-genome sequencing
- 1 August 2008
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature Methods
- Vol. 5 (10), 865-867
- https://doi.org/10.1038/nmeth.1249
Abstract
Identifying the molecular lesions in mutants isolated in forward genetic screens can be a laborious process. A proof-of-principle study in Caenorhabditis elegans now shows that this can be achieved rapidly by whole-genome deep sequencing. Identification of the molecular lesion in Caenorhabditis elegans mutants isolated through forward genetic screens usually involves time-consuming genetic mapping. We used Illumina deep sequencing technology to sequence a complete, mutant C. elegans genome and thus pinpointed a single-nucleotide mutation in the genome that affects a neuronal cell fate decision. This constitutes a proof-of-principle for using whole-genome sequencing to analyze C. elegans mutants.This publication has 8 references indexed in Scilit:
- Whole-genome sequencing and variant discovery in C. elegansNature Methods, 2008
- Genetic Screens forCaenorhabditis elegansMutants Defective in Left/Right Asymmetric Neuronal Fate SpecificationGenetics, 2007
- Whole-genome re-sequencingCurrent Opinion in Genetics & Development, 2006
- Rapid single nucleotide polymorphism mapping in C. elegansBMC Genomics, 2005
- A transcriptional regulatory cascade that controls left/right asymmetry in chemosensory neurons ofC. elegansJournal of Bone and Joint Surgery, 2003
- Genomic mapping by fingerprinting random clones: A mathematical analysisGenomics, 1988
- The genetics of Caenorhabditis elegans.1974
- THE GENETICS OF CAENORHABDITIS ELEGANSGenetics, 1974