Ngā hua rapu - Pall I. Olason

Whakamahine hua
  1. 1
    Lessons learned from implementing a national infrastructure in Sweden for storage and analysis of next-generation sequencing data

    Lessons learned from implementing a national infrastructure in Sweden for storage and analysis of next-generation sequencing data mā Samuel Lampa, Martin Dahlö, Pall I. Olason, Jonas Hagberg, Ola Spjuth

    I whakaputaina 2013
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    Artigo
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  2. 2
    TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data

    TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data mā Jesper Eisfeldt, Francesco Vezzi, Pall I. Olason, Daniel Nilsson, Anna Lindstrand

    I whakaputaina 2017
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  3. 3
    TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data

    TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data mā Jesper Eisfeldt, Francesco Vezzi, Pall I. Olason, Daniel Nilsson, Anna Lindstrand

    I whakaputaina 2017
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  4. 4
    Demographic Divergence History of Pied Flycatcher and Collared Flycatcher Inferred from Whole-Genome Re-sequencing Data

    Demographic Divergence History of Pied Flycatcher and Collared Flycatcher Inferred from Whole-Genome Re-sequencing Data mā Krystyna Nadachowska‐Brzyska, Reto Burri, Pall I. Olason, Takeshi Kawakami, Linnéa Smeds, Hans Ellegren

    I whakaputaina 2013
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    Artigo
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  5. 5
    Estimation of linkage disequilibrium and interspecific gene flow in <i><scp>F</scp>icedula</i> flycatchers by a newly developed 50k single‐nucleotide polymorphism array

    Estimation of linkage disequilibrium and interspecific gene flow in <i><scp>F</scp>icedula</i> flycatchers by a newly developed 50k single‐nucleotide polymorphism array mā Takeshi Kawakami, Niclas Backström, Reto Burri, Arild Husby, Pall I. Olason, Amber M. Rice, Murielle Ålund, Anna Qvarnström, Hans Ellegren

    I whakaputaina 2014
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    Artigo
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  6. 6
    De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

    De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data mā Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall I. Olason, Lars Feuk, Ulf Gyllensten

    I whakaputaina 2018
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    Artigo
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  7. 7
    The genomic landscape of species divergence in Ficedula flycatchers

    The genomic landscape of species divergence in Ficedula flycatchers mā Hans Ellegren, Linnéa Smeds, Reto Burri, Pall I. Olason, Niclas Backström, Takeshi Kawakami, Axel Künstner, Hannu Mäkinen, Krystyna Nadachowska‐Brzyska, Anna Qvarnström, Severin Uebbing, Jochen B. W. Wolf

    I whakaputaina 2012
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    Artigo
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  8. 8
    A human phenome-interactome network of protein complexes implicated in genetic disorders

    A human phenome-interactome network of protein complexes implicated in genetic disorders mā Kasper Lage, E. Olof Karlberg, Zenia M. Størling, Pall I. Olason, Anders Gorm Pedersen, Olga Rigina, Anders M. Hinsby, Zeynep Tümer, Flemming Pociot, Niels Tommerup, Yves Moreau, Søren Brunak

    I whakaputaina 2007
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    Artigo
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  9. 9
    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants

    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants mā M. Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz de Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt

    I whakaputaina 2020
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  10. 10
    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants

    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants mā M. Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz de Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt

    I whakaputaina 2020
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  11. 11
    Detection of sharing by descent, long-range phasing and haplotype imputation

    Detection of sharing by descent, long-range phasing and haplotype imputation mā Augustine Kong, Gísli Másson, Michael L. Frigge, Arnaldur Gylfason, Pasha Zusmanovich, Guðmar Þorleifsson, Pall I. Olason, Andrés Ingason, Stacy Steinberg, Þórunn Rafnar, Patrick Sulem, Magali Mouy, Frosti Jónsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hreinn Stefánsson, Kāri Stefánsson

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Complete human recombination maps

    Complete human recombination maps mā Gunnar Pálsson, Marteinn T. Hardarson, Hákon Jónsson, Valgerður Steinthórsdóttir, Ólafur Andri Stefánsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Pall I. Olason, Arnaldur Gylfason, Gísli Másson, Unnur Þorsteinsdóttir, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson

    I whakaputaina 2025
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    Artigo
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  13. 13
    Linked selection and recombination rate variation drive the evolution of the genomic landscape of differentiation across the speciation continuum of <i>Ficedula</i> flycatchers

    Linked selection and recombination rate variation drive the evolution of the genomic landscape of differentiation across the speciation continuum of <i>Ficedula</i> flycatchers mā Reto Burri, Alexander Nater, Takeshi Kawakami, Carina F. Mugal, Pall I. Olason, Linnéa Smeds, Alexander Suh, Ludovic Dutoit, Stanislav Bureš, László Zsolt Garamszegi, Silje Hogner, Juan Moreno, Anna Qvarnström, Milan Ružić, S. A. Sæther, Glenn‐Peter Sætre, János Török, Hans Ellegren

    I whakaputaina 2015
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    Artigo
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  14. 14
    Sequence variants affecting the genome-wide rate of germline microsatellite mutations

    Sequence variants affecting the genome-wide rate of germline microsatellite mutations mā Snædís Kristmundsdóttir, Hákon Jónsson, Marteinn T. Hardarson, Gunnar Pálsson, Doruk Beyter, Hannes P. Eggertsson, Arnaldur Gylfason, Garðar Sveinbjörnsson, Guillaume Holley, Ólafur Andri Stefánsson, Gísli H. Halldórsson, Sigurgeir Ólafsson, Gudny A. Arnadottir, Pall I. Olason, Ögmundur Eiríksson, Gísli Másson, Unnur Þorsteinsdóttir, Þórunn Rafnar, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson

    I whakaputaina 2023
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    Artigo
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  15. 15
    SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

    SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population mā Adam Ameur, Johan Dahlberg, Pall I. Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kähäri, Pär Lundin, Huiwen Che, Jessada Thutkawkorapin, Jesper Eisfeldt, Samuel Lampa, Mats Dahlberg, Jonas Hagberg, Niclas Jareborg, Ulrika Liljedahl, Inger Jonasson, Åsa Johansson, Lars Feuk, Joakim Lundeberg, Ann‐Christine Syvänen, Sverker Lundin, Daniel Nilsson, Björn Nystedt, Patrik K. E. Magnusson, Ulf Gyllensten

    I whakaputaina 2017
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    Artigo
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  16. 16
    Parental origin of sequence variants associated with complex diseases

    Parental origin of sequence variants associated with complex diseases mā Augustine Kong, Valgerður Steinthórsdóttir, Gísli Másson, Guðmar Þorleifsson, Patrick Sulem, Søren Besenbacher, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Kári Kristinsson, Aðalbjörg Jónasdóttir, Michael L. Frigge, Arnaldur Gylfason, Pall I. Olason, Sigurjón A. Guðjónsson, Sverrir T. Sverrisson, Simon Stacey, Bárður Sigurgeirsson, Kristrún R. Benediktsdóttir, Helgi Sigurðsson, Þorvaldur Jónsson, Rafn Benediktsson, Jón Ólafsson, Oskar T. Johannsson, Ástráður B. Hreiðarsson, Gunnar Sigurðsson, Anne C. Ferguson‐Smith, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Kāri Stefánsson

    I whakaputaina 2009
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    Artigo
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  17. 17
    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia mā George Kirov, Andrew Pocklington, Peter Holmans, Dobril Ivanov, Masashi Ikeda, Douglas M. Ruderfer, Jennifer L. Moran, Kimberly Chambert, Драга Тончева, L. Georgieva, Detelina Grozeva, Marija Fjodorova, R Wollerton, Elliott Rees, Ivan Nikolov, Louie N. van de Lagemaat, Àlex Bayés, E Fernández, Pall I. Olason, Yvonne Böttcher, Noboru H. Komiyama, Mark O. Collins, Jyoti S. Choudhary, Kāri Stefánsson, Hreinn Stefánsson, Seth G. N. Grant, Shaun Purcell, Pamela Sklar, Michael O’Donovan, Michael J. Owen

    I whakaputaina 2011
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    Artigo
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  18. 18
    Large-scale plasma proteomics comparisons through genetics and disease associations

    Large-scale plasma proteomics comparisons through genetics and disease associations mā Grímur Hjörleifsson Eldjárn, Egil Ferkingstad, Sigrún H. Lund, Hannes Helgason, Ólafur Þ. Magnússon, Kristbjörg Gunnarsdóttir, Thorunn A. Olafsdottir, Bjarni V. Halldórsson, Pall I. Olason, Florian Zink, Sigurjón A. Guðjónsson, Garðar Sveinbjörnsson, Magnus I. Magnusson, Agnar Helgason, Ásmundur Oddsson, Gísli H. Halldórsson, Magnús K. Magnússon, Saedís Saevarsdóttir, Thjodbjorg Eiriksdottir, Gísli Másson, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Páll Melsted, Jona Saemundsdottir, Gudmundur L. Norddahl, Guðmar Þorleifsson, Magnús Ö. Úlfarsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Patrick Sulem, Kāri Stefánsson

    I whakaputaina 2023
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    Artigo
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  19. 19
    Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations

    Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations mā Grímur Hjörleifsson Eldjárn, Egil Ferkingstad, Sigrún H. Lund, Hannes Helgason, Ólafur Þ. Magnússon, Kristbjörg Gunnarsdóttir, Thorunn A. Olafsdottir, Bjarni V. Halldórsson, Pall I. Olason, Florian Zink, Sigurjón A. Guðjónsson, Garðar Sveinbjörnsson, Magnus I. Magnusson, Agnar Helgason, Ásmundur Oddsson, Gísli H. Halldórsson, Magnús K. Magnússon, Saedís Saevarsdóttir, Thjodbjorg Eiriksdottir, Gísli Másson, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Páll Melsted, Jona Saemundsdottir, Gudmundur L. Norddahl, Guðmar Þorleifsson, Magnús Ö. Úlfarsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Patrick Sulem, Kāri Stefánsson

    I whakaputaina 2024
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    Errata/Corrigenda
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  20. 20
    Sequence diversity lost in early pregnancy

    Sequence diversity lost in early pregnancy mā Gudny A. Arnadottir, Hákon Jónsson, Tanja Schlaikjær Hartwig, Jennifer R. Gruhn, Peter Möller, Arnaldur Gylfason, David Westergaard, Andrew C. Chan, Ásmundur Oddsson, Lilja Stefánsdóttir, Louise le Roux, Valgerður Steinthórsdóttir, Kristjan H. S. Moore, Sigurgeir Ólafsson, Pall I. Olason, Hannes P. Eggertsson, Gísli H. Halldórsson, G. Bragi Walters, Hreinn Stefánsson, Sigurjón A. Guðjónsson, Gunnar Pálsson, Brynjar Ö. Jensson, Rún Friðriksdóttir, Jesper Friis Petersen, Agnar Helgason, Gudmundur L. Norddahl, Palle Duun Rohde, Jona Saemundsdottir, Ólafur Þ. Magnússon, Bjarni V. Halldórsson, Sofie Bliddal, Karina Banasik, Daníel F. Guðbjartsson, Mette Nyegaard, Patrick Sulem, Unnur Thorsteinsdottir, Eva R. Hoffmann, Henriette Svarre Nielsen, Kāri Stefánsson

    I whakaputaina 2025
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    Artigo
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