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|Title:||Exome versus transcriptome sequencing in identifying coding region variants||Authors:||Ku, C.-S.
|Issue Date:||Apr-2012||Citation:||Ku, C.-S., Wu, M., Cooper, D.N., Naidoo, N., Pawitan, Y., Pang, B., Iacopetta, B., Soong, R. (2012-04). Exome versus transcriptome sequencing in identifying coding region variants. Expert Review of Molecular Diagnostics 12 (3) : 241-251. ScholarBank@NUS Repository. https://doi.org/10.1586/erm.12.10||Abstract:||The advent of next-generation sequencing technologies has revolutionized the study of genetic variation in the human genome. Whole-genome sequencing currently represents the most comprehensive strategy for variant detection genome-wide but is costly for large sample sizes, and variants detected in noncoding regions remain largely uninterpretable. By contrast, whole-exome sequencing has been widely applied in the identification of germline mutations underlying Mendelian disorders, somatic mutations in various cancers and de novo mutations in neurodevelopmental disorders. Since whole-exome sequencing focuses upon the entire set of exons in the genome (the exome), it requires additional exome-enrichment steps compared with whole-genome sequencing. Although the availability of multiple commercial exome-enrichment kits has made whole-exome sequencing technically feasible, it has also added to the overall cost. This has led to the emergence of transcriptome (or RNA) sequencing as a potential alternative approach to variant detection within protein coding regions, since the transcriptome of a given tissue represents a quasi-complete set of transcribed genes (mRNAs) and other noncoding RNAs. A further advantage of this approach is that it bypasses the need for exome enrichment. Here we discuss the relative merits and limitations of these approaches as they are applied in the context of variant detection within gene coding regions. © 2012 Expert Reviews Ltd.||Source Title:||Expert Review of Molecular Diagnostics||URI:||http://scholarbank.nus.edu.sg/handle/10635/108846||ISSN:||14737159||DOI:||10.1586/erm.12.10|
|Appears in Collections:||Staff Publications|
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