Výsledky vyhledávání - Sipos, Botond

t2prhd: a tool to study the patterns of repeat evolution Autor Sipos, Botond, Somogyi, Kálmán, Andó, István, Pénzes, Zsolt

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PhyloSim - Monte Carlo simulation of sequence evolution in the R statistical computing environment Autor Sipos, Botond, Massingham, Tim, Jordan, Gregory E, Goldman, Nick

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An Improved Protocol for Sequencing of Repetitive Genomic Regions and Structural Variations Using Mutagenesis and Next Generation Sequencing Autor Sipos, Botond, Massingham, Tim, Stütz, Adrian M., Goldman, Nick

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Error correction enables use of Oxford Nanopore technology for reference-free transcriptome analysis Autor Sahlin, Kristoffer, Sipos, Botond, James, Phillip L., Medvedev, Paul

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Phylogenetic Quantification of Intra-tumour Heterogeneity Autor Schwarz, Roland F., Trinh, Anne, Sipos, Botond, Brenton, James D., Goldman, Nick, Markowetz, Florian

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Toward practical high-capacity low-maintenance storage of digital information in synthesised DNA Autor Goldman, Nick, Bertone, Paul, Chen, Siyuan, Dessimoz, Christophe, LeProust, Emily M., Sipos, Botond, Birney, Ewan

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Amino Acid Changes in Disease-Associated Variants Differ Radically from Variants Observed in the 1000 Genomes Project Dataset Autor de Beer, Tjaart A. P., Laskowski, Roman A., Parks, Sarah L., Sipos, Botond, Goldman, Nick, Thornton, Janet M.

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Generation of a Transcriptional Radiation Exposure Signature in Human Blood Using Long-Read Nanopore Sequencing Autor Cruz-Garcia, Lourdes, O’Brien, Grainne, Sipos, Botond, Mayes, Simon, Love, Michael I., Turner, Daniel J., Badie, Christophe

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Sessile hemocytes as a hematopoietic compartment in Drosophila melanogaster Autor Márkus, Róbert, Laurinyecz, Barbara, Kurucz, Éva, Honti, Viktor, Bajusz, Izabella, Sipos, Botond, Somogyi, Kálmán, Kronhamn, Jesper, Hultmark, Dan, Andó, István

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In Vivo Validation of Alternative FDXR Transcripts in Human Blood in Response to Ionizing Radiation Autor Cruz-Garcia, Lourdes, O’Brien, Grainne, Sipos, Botond, Mayes, Simon, Tichý, Aleš, Sirák, Igor, Davídková, Marie, Marková, Markéta, Turner, Daniel J., Badie, Christophe

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Systematic evaluation of spliced alignment programs for RNA-seq data Autor Engström, Pär G, Steijger, Tamara, Sipos, Botond, Grant, Gregory R, Kahles, André, Rätsch, Gunnar, Goldman, Nick, Hubbard, Tim J, Harrow, Jennifer, Guigó, Roderic, Bertone, Paul

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Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome Autor Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H

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SMIM1 underlies the Vel blood group and influences red blood cell traits Autor Cvejic, Ana, Haer-Wigman, Lonneke, Stephens, Jonathan C, Kostadima, Myrto, Smethurst, Peter A, Frontini, Mattia, van den Akker, Emile, Bertone, Paul, Bielczyk-Maczyńska, Ewa, Farrow, Samantha, Fehrmann, Rudolf SN, Gray, Alan, de Haas, Masja, Haver, Vincent G, Jordan, Gregory, Karjalainen, Juha, Kerstens, Hindrik HD, Kiddle, Graham, Lloyd-Jones, Heather, Needs, Malcolm, Poole, Joyce, Soussan, Aicha Ait, Rendon, Augusto, Rieneck, Klaus, Sambrook, Jennifer G, Schepers, Hein, Silljé, Herman H W, Sipos, Botond, Swinkels, Dorine, Tamuri, Asif U, Verweij, Niek, Watkins, Nicholas A, Westra, Harm-Jan, Stemple, Derek, Franke, Lude, Soranzo, Nicole, Stunnenberg, Hendrik G, Goldman, Nick, van der Harst, Pim, van der Schoot, C Ellen, Ouwehand, Willem H, Albers, Cornelis A

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