Torthaí cuardaigh - Sipos, Botond

t2prhd: a tool to study the patterns of repeat evolution de réir 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 de réir 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 de réir 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 de réir Sahlin, Kristoffer, Sipos, Botond, James, Phillip L., Medvedev, Paul

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Phylogenetic Quantification of Intra-tumour Heterogeneity de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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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