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Joanna Kołsut, Paulina Borówka, Błażej Marciniak, Ewelina Wójcik, Arkadiusz Wojtasik, Dominik Strapagiel and Jarosław Dastych

-associated genes in avian pathogenic Escherichia coli by multiplex polymerase chain reaction. Avian Dis 2005, 49, 269–273. 5. Ge X.Z., Jiang J., Pan Z., Hu L., Wang S., Wang H., Fan H.: Comparative genomic analysis shows that avian pathogenic Escherichia coli isolate IMT5155 (O2:K1:H5; ST complex 95, ST140) shares close relationship with ST95 APEC O1: K1 and human ExPEC O18:K1 strains. PloS One 2014, 9, e112048. 6. Giufré M., Accogli M., Graziani C., Busani L., Cerquetti M.: Whole-genome sequences of multidrug-resistant Escherichia coli strains sharing the same

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Kevan M.A. Gartland, Munis Dundar, Tommaso Beccari, Mariapia Viola Magni and Jill S. Gartland

References 1. Fleischmann RD, Adams MD, White O, Clayton RA. Whole-genome random sequencing and assembly of Haemophilus influenzae Rd. Science 1995; 269: 496-512. 2. C. elegans Sequencing Consortium. Genome sequence of the nematode C. elegans: a platform for investigating biology. Science 1998; 282: 2012-2018. 3. Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R. Initial sequencing and analysis of the human genome. Nature, 2001; 409: 860

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Sylwia Keller-Przybyłkowicz and Małgorzata U. Korbin

References Alston F.H., Phillips K.L., Evans K.M., 2000. A Malus gene list. Acta Hort. 538: 561-570. Andersen J.R., Lübberstedt T., 2003. Functional markers in plants. Trends Plant Sci. 8(11): 554-560. Antanaviciute L., Fernandez-Fernandes F., Jansen J., Banchi E., Evans K.M., Viola R., et al., 2012. Development of a dense SNP-based linkage map of apple rootstock progeny using the Malus infinium whole genome genotyping array. Genomics 13: 203. Boudichevskaia A., Flachowsky

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Aneta Słomka, Dorota Siwińska, Elżbieta Wolny, Kristin Kellner and Elżbieta Kuta

culture. In: Vasal IK [ed.], Perspective in Plant Cell and Tissue Culture , 113-144. Academic Press. Beaulieu JM, Smith S, and Leitch IJ. 2010. On the tempo of genome size evolution in Angiosperms. Journal of Botany , doi: 10.1155/2010/989152. Bolkhovskikh Z, Grif V, Matvejeva T, and Zakharyeva O. 1969. Chromosome Number of Flowering Plants . Academy of Science of the USSR. V.L, Komarov Botanical Institute. Bone E, and Farres A. 2001. Trends and rates of microevolution in plants. Genetica

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Anna Muszewska

indicate widespread neofunctionalization of yeast genes after whole-genome duplication. Genetics, 175(3), 1341-1350. doi:10.1534/genetics.106.066951 Capy, P., Gasperi, G., Biémont, C. & Bazin, C. 2000. Stress and transposable elements: coevolution or useful parasites? Heredity, 85 ( Pt 2), 101-106. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11012710 Cissé, O.H., Almeida, J.M.G.C.F., Fonseca, A., Kumar, A.A., Salojärvi, J., Overmyer, K. & Pagni, M. 2013. Genome sequencing of the plant pathogen Taphrina deformans, the causal agent of

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Sandra Cichorz, Maria Gośka and Monika Rewers

REFERENCES A dati S, and S hiotani I. 1962. The cytotaxonomy of the genus Miscanthus and its phylogenic status. Bulletin of the Faculty of Agriculture Mie University 25: 1–24. B ennett MD. 1987. Variation in genomic form in plants and its ecological implications. New Phytologist 106: 177–200. B ennett MD, and L eitch IJ. 2005. Plant genome size research: a field in focus. Annals of Botany 95: 1–6. B ennetzen JL, M a J, and D evos KM. 2005. Mechanisms of recent genome size variation in flowering plants. Annals of Botany 95

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Theano Lazaridou, Chryssanthi Pankou, Ioannis Xynias and Demetrios Roupakias

culture in wheat ( Triticum aestivum L.). Genome 38: 158–165. G haemi M, and S arrafi A. 1994. The effect of the “D” genome from synthetic wheat lines in anther culture responses. Plant Breeding 112: 76–79. H e DG, and O uyang JW. 1984. Callus and plantlet formation from cultured wheat anthers at different developmental stages. Plant Science Letters 33: 71–79. H u TC, and K asha KJ. 1997. Improvement of isolated microspore culture of wheat Triticum aestivum L. through ovary co-culture. Plant Cell Reports 16: 520–525. H ennawy EI

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Abdel-Rahman Moustafa Abdel-Wahab Mohamed, Tomasz Jęcz and Małgorzata Korbin

Graduate Studies, University of Guelph, Canada. Bringhurst R.S., Senanayake Y.D.A. 1966. The evolutionary significance of natural Fragaria chiloensis × F. vesca hybrids resulting from unreduced gametes. Amer. J. Bot. 53: 1000-1006. DOI: 10.2307/2440678. Brown T.A. 2002. Genomes. 2nd edition. Wiley-Less, Oxford, UK. Cekic C., Battey N.H., Wilkinson M.J. 2001. The potential of ISSR- PCR primer pair combinations for genetic linkage analysis using the Seasonal Flowering Locus in Fragaria vesca as a model. Theor. Appl. Genet

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Zelimir Kurtanjek

-46. 8. Clare A, “Machine learning and data mining for yeast functional genomics”, PhD Thesis, 2003, University of Wales, Aberystwyth, UK. 9. Huttenhower C., Mutungu K.M., Indik N., Yang W., Schroeder M., Forman J.J., Troyanskaya O.G., Coller H. Detailing regulatory networks through large scale data integration. Bioinformatics 2009; 25(24): 3267-3274. 10. Taymaz-Nikerel H, Cankorur-Cetinkaya A, Kirdar B. Genome-Wide Transcriptional Response of Saccharomyces cerevisiae to Stress-Induced Perturbations. Front Bioeng Biotechnol 2016; 4

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J. Zeyland, Ł. Wolko, J. Bocianowski, M. Szalata, R. Słomski, A.M. Dzieduszycki, M. Ryba, H. Przystałowska and D. Lipiński

References Achilli A, Bonfiglio S, Olivieri A, Malusg A, Pala M, Hooshiar Kashani B, Perego UA, Ajmone-Marsan P, Liotta L, Semino O, Bandelt HJ, Ferretti L, Torroni A ( 2009 ) The multifaceted origin of taurine cattle reflected by the mitochondrial genome. PLoS One 4: e5753. Achilli A, Olivieri A, Pellecchia M, Uboldi C, Colli L, Al-Zahery N, Accetturo M, Pala M, Hooshiar Kashani B, Perego UA, Battaglia V, Fornarino S, Kalamati J, Houshmand M, Negrini R, Semino O, Richards M, Macaulay V, Ferretti L, Bandelt HJ, Ajmone