ENHANCING GENETIC MERIT OF DAIRY CATTLE THROUGH GENOME SELECTION AND ANALYSIS
Title: Quality assessment parameters for EST-derived SNPs from catfish
| Wang, Shaolin - AUBURN UNIV |
| Sha, Zhenxia - AUBURN UNIV |
| Liu, Hong - AUBURN UNIV |
| Xu, Peng - AUBURN UNIV |
| Somridhavej, Benjaporn - AUBURN UNIV |
| Peatmen, Eric - AUBURN UNIV |
| Kucuktas, Huseyin - AUBURN UNIV |
| Liu, Zhanjiang - AUBURN UNIV |
Submitted to: Biomed Central (BMC) Genomics
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: September 10, 2008
Publication Date: September 30, 2008
Citation: Wang, S., Sha, Z., Sonstegard, T.S., Liu, H., Xu, P., Somridhavej, B., Peatmen, E., Kucuktas, H., Liu, Z. 2008. Quality assessment parameters for EST-derived SNPs from catfish. Biomed Central (BMC) Genomics. 30(9):450.
Interpretive Summary: SNPs are most abundant, codominantly inherited, and sequence-tagged markers. They are highly adaptable to large-scale automated genotyping, and therefore, are most suitable for association studies and applicable to comparative genome analysis. However, discovery of SNPs requires genome sequencing efforts through whole genome sequencing or deep sequencing of reduced representation libraries. Such genome resources are not yet available for many species including catfish. A large resource of ESTs is to become available in catfish allowing identification of large number of SNPs, but reliability of EST-derived SNPs are relatively low because of sequencing errors. This project was designed to answer some of the questions relevant to quality assessment of EST-derived SNPs.
Two factors were found to be most significant for validation of EST-derived SNPs: the contig size and the minor allele sequence frequency. The larger the contigs were, the greater the validation rate although the validation rate was reasonably high when the contig sizes were equal to or larger than four with the minor allele sequence being represented at least twice in the contigs. Sequence quality surrounding the SNP under test is also crucially important. While these findings were not unexpected, PCR extension appeared to be limited to a very short distance, prohibiting successful genotyping when an intron was present, a surprising finding.
Stringent quality assessment measures should be used when working with EST-derived SNPs. In particular, contigs containing four or more ESTs should be used and the minor allele sequence should be represented at least twice. Genotyping primers should be designed from a single exon, completely avoiding introns. Application of such quality assessment measures, along with large resources of ESTs, should provide effective means for SNP identification in species where genome sequence resources are lacking.