Basit öğe kaydını göster

dc.contributor.authorMAASS, A.
dc.contributor.authorMUNOZ, C.
dc.contributor.authorORELLANA, A.
dc.contributor.authorDI GENOVA, A.
dc.contributor.authorAravena, Andres Octavıo
dc.contributor.authorHINRICHSEN, P.
dc.date.accessioned2021-03-05T11:43:46Z
dc.date.available2021-03-05T11:43:46Z
dc.identifier.citationMUNOZ C., DI GENOVA A., MAASS A., ORELLANA A., HINRICHSEN P., Aravena A. O. , "Vitis vinifera Genome Annotation Improvement Using Next-Generation Sequencing Technologies and NCBI Public Data", 10th International Conference on Grapevine Breeding and Genetics, New-York, Amerika Birleşik Devletleri, 1 - 05 Ağustos 2010, cilt.1046, ss.349-356
dc.identifier.othervv_1032021
dc.identifier.otherav_a99aed79-ee68-40cb-948a-9a544cb1a2d9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/113290
dc.description.abstractGrapevine (Vitis spp.) is the most widely cultivated and economically important fruit crop. Even though the genus exhibits a huge diversity present in more than 50 species, the main products are derived from Vitis vinifera whose origin is from the Southern Caucasus to central Europe. Besides, grapevine constitutes per se a model for the study of woody species. In the Southern hemisphere, Chile has become a large wine producer and the main exporter of table grapes. Our present aim is to develop a bioinformatic platform able to identify SNPs, detect splicing variants and annotate new genes, all tools that could finally give support to select traits of interest. We analyzed data from 18 Vitis species, including cultivars of V. vinifera and wild species of the Vitis genus. The data was obtained by Illumina sequencing from two RNA-seq experiments performed by Zenoni et al. (2010) and Myles et al. (2010), both available at NCBI. The first one reported data from cv. 'Corvina' while the latter from 'Pinot Noir', 'Inbred Pinot Noir' and 15 other cultivated cultivars and wild species. The sequence reads were aligned onto the 12X draft sequence of the 'Pinot Noir'-derived 40024 genome whereas the reported data was aligned onto 8X genome. The alignments were analyzed to detect alternative splicing events and expressed single nucleotide polymorphisms (SNPs). We aligned 116,665,608 reads selecting hits with at most two mismatches. Over 55% of the reads showed only one alignment to the reference genome, 19% had multiple matches and 26% of them were unmatched. Preliminary results detected 387,278 putative SNPs using a Q-score of 20, coverage over 8x and a variability of over 25%. This study will help to improve the current Vitis genome annotation as well as to increase our knowledge about Vitis phylogenetic relationships. Our next step will be to search for new genes as well as spliced variants within Vitis genus. Future perspectives involve the integration of transcriptomic and proteomic data.
dc.language.isoeng
dc.subjectFitopatoloji
dc.subjectTarım Bilimleri
dc.subjectTarımsal Bilimler
dc.subjectZiraat
dc.subjectBahçe Bitkileri
dc.subjectBitki Koruma
dc.subjectBİTKİ BİLİMLERİ
dc.subjectBitki ve Hayvan Bilimleri
dc.subjectTarım ve Çevre Bilimleri (AGE)
dc.subjectBAHÇE BİTKİLERİ
dc.titleVitis vinifera Genome Annotation Improvement Using Next-Generation Sequencing Technologies and NCBI Public Data
dc.typeBildiri
dc.contributor.departmentUniversidad Andres Bello , ,
dc.identifier.volume1046
dc.contributor.firstauthorID100634


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster