KmerStream: streaming algorithms for k-mer abundance estimation von Melsted, Páll, Halldórsson, Bjarni V

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Max point-tolerance graphs von Catanzaro, Daniele, Chaplick, Steven, Felsner, Stefan, Halldórsson, Bjarni V., Halldórsson, Magnús M., Hixon, Thomas, Stacho, Juraj

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popSTR: population-scale detection of STR variants von Kristmundsdóttir, Snædís, Sigurpálsdóttir, Brynja D, Kehr, Birte, Halldórsson, Bjarni V

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Streaming Algorithms for Independent Sets in Sparse Hypergraphs von Halldórsson, Bjarni V., Halldórsson, Magnús M., Losievskaja, Elena, Szegedy, Mario

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The nature of nurture: Effects of parental genotypes von Kong, Augustine, Thorleifsson, Gudmar, Frigge, Michael L, Vilhjalmsson, Bjarni J, Young, Alexander I, Thorgeirsson, Thorgeir E, Benonisdottir, Stefania, Oddsson, Asmundur, Halldorsson, Bjarni V, Masson, Gisli, Gudbjartsson, Daniel F, Helgason, Agnar, Bjornsdottir, Gyda, Thorsteinsdottir, Unnur, Stefansson, Kari

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A hybrid micro-macroevolutionary approach to gene tree reconstruction von Durand, Dannie, Halldórsson, Bjarni V, Vernot, Benjamin

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Variable number tandem repeats mediate the expression of proximal genes von Bakhtiari, Mehrdad, Park, Jonghun, Ding, Yuan-Chun, Shleizer-Burko, Sharona, Neuhausen, Susan L., Halldórsson, Bjarni V., Stefánsson, Kári, Gymrek, Melissa, Bafna, Vineet

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Characterizing mutagenic effects of recombination through a sequence-level genetic map von Halldorsson, Bjarni V, Palsson, Gunnar, Stefansson, Olafur A, Jonsson, Hakon, Hardarson, Marteinn T, Eggertsson, Hannes P, Gunnarsson, Bjarni, Oddsson, Asmundur, Halldorsson, Gisli H, Zink, Florian, Gudjonsson, Sigurjon A, Frigge, Michael L, Thorleifsson, Gudmar, Sigurdsson, Asgeir, Stacey, Simon N, Sulem, Patrick, Masson, Gisli, Helgason, Agnar, Gudbjartsson, Daniel F, Thorsteinsdottir, Unnur, Stefansson, Kari

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Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits von Beyter, Doruk, Ingimundardottir, Helga, Oddsson, Asmundur, Eggertsson, Hannes P., Bjornsson, Eythor, Jonsson, Hakon, Atlason, Bjarni A., Kristmundsdottir, Snaedis, Mehringer, Svenja, Hardarson, Marteinn T., Gudjonsson, Sigurjon A., Magnusdottir, Droplaug N., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Kristjansson, Ragnar P., Sverrisson, Sverrir T., Holley, Guillaume, Palsson, Gunnar, Stefansson, Olafur A., Eyjolfsson, Gudmundur, Olafsson, Isleifur, Sigurdardottir, Olof, Torfason, Bjarni, Masson, Gisli, Helgason, Agnar, Thorsteinsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel F., Sulem, Patrick, Magnusson, Olafur T., Halldorsson, Bjarni V., Stefansson, Kari

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The minimum vulnerability problem on specific graph classes von Aoki, Yusuke, Halldórsson, Bjarni V., Halldórsson, Magnús M., Ito, Takehiro, Konrad, Christian, Zhou, Xiao

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PopIns: population-scale detection of novel sequence insertions von Kehr, Birte, Melsted, Páll, Halldórsson, Bjarni V

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NCOurd: modelling length distributions of NCO events and gene conversion tracts von Hardarson, Marteinn T, Palsson, Gunnar, Halldorsson, Bjarni V

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Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies von RIVADENEIRA, Fernando, STYRKARSDOTTIR, Unnur, CUPPLES, L. Adrienne, DELOUKAS, Panagiotis, DEMISSIE, Serkalem, GRUNDBERG, Elin, HOFMAN, Albert, KONG, Augustine, KARASIK, David, VAN MEURS, Joyce B, OOSTRA, Ben, PASTINEN, Tomi, ESTRADA, Karol, POLS, Huibert A. P, SIGURDSSON, Gunnar, SORANZO, Nicole, THORLEIFSSON, Gudmar, THORSTEINSDOTTIR, Unnur, WILLIAMS, Frances M. K, WILSON, Scott G, YANHUA ZHOU, RALSTON, Stuart H, VAN DUIJN, Cornelia M, HALLDORSSON, Bjarni V, SPECTOR, Timothy, KIEL, Douglas P, STEFANSSON, Kari, IOANNIDIS, John P. A, UITTERLINDEN, André G, HSU, Yi-Hsiang, RICHARDS, J. Brent, ZILLIKENS, M. Carola, KAWOURA, Fotini K, AMIN, Najaf, AULCHENKO, Yurii S

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PopAlu: population-scale detection of Alu polymorphisms von Qian, Yu, Kehr, Birte, Halldórsson, Bjarni V

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DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism von Aguiar, Derek, Halldórsson, Bjarni V, Morrow, Eric M, Istrail, Sorin

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GGTyper: genotyping complex structural variants using short-read sequencing data von Mirus, Tim, Lohmayer, Robert, Döhring, Clementine, Halldórsson, Bjarni V, Kehr, Birte

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Methylation of Bone SOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women von Reppe, Sjur, Noer, Agate, Grimholt, Runa M, Halldórsson, Bjarni V, Medina‐Gomez, Carolina, Gautvik, Vigdis T, Olstad, Ole Kristoffer, Berg, Jens Petter, Datta, Harish, Estrada, Karol, Hofman, Albert, Uitterlinden, André G, Rivadeneira, Fernando, Lyle, Robert, Collas, Philippe, Gautvik, Kaare M

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Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly von Holley, Guillaume, Beyter, Doruk, Ingimundardottir, Helga, Moller, Peter L., Kristmundsdottir, Snodis, Eggertsson, Hannes P., Halldorsson, Bjarni

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GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs von Eggertsson, Hannes P., Kristmundsdottir, Snaedis, Beyter, Doruk, Jonsson, Hakon, Skuladottir, Astros, Hardarson, Marteinn T., Gudbjartsson, Daniel F., Stefansson, Kari, Halldorsson, Bjarni V., Melsted, Pall

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read_haps: using read haplotypes to detect same species contamination in DNA sequences von Eggertsson, Hannes P, Halldorsson, Bjarni V

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