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Simplified and efficient quantification of low-abundance proteins at very high multiplex via targeted mass spectrometry.

Burgess MW, Keshishian H, Mani DR, Gillette MA, Carr SA. Simplified and efficient quantification of low-abundance proteins at very high multiplex via targeted mass spectrometry. Mol Cell Proteomics. 2014;13(4):1137-49. doi:10.1074/mcp.M113.034660

Guidelines for investigating causality of sequence variants in human disease.

Macarthur DG, Manolio TA, Dimmock DP, et al. Guidelines for investigating causality of sequence variants in human disease. Nature. 2014;508(7497):469-76. doi:10.1038/nature13127

Selection of unique Escherichia coli clones by random amplified polymorphic DNA (RAPD): Evaluation by whole genome sequencing.

Nielsen KL, Godfrey PA, Stegger M, Andersen PS, Feldgarden M, Frimodt-Møller N. Selection of unique Escherichia coli clones by random amplified polymorphic DNA (RAPD): Evaluation by whole genome sequencing. J Microbiol Methods. 2014;103:101-3. doi:10.1016/j.mimet.2014.05.018

Improving accuracy of rare variant imputation with a two-step imputation approach.

Kreiner-Møller E, Medina-Gomez C, Uitterlinden AG, Rivadeneira F, Estrada K. Improving accuracy of rare variant imputation with a two-step imputation approach. Eur J Hum Genet. 2015;23(3):395-400. doi:10.1038/ejhg.2014.91

Genetic validation of a therapeutic target in a mouse model of ALS.

de Boer S, Koszka K, Kiskinis E, Suzuki N, Davis-Dusenbery BN, Eggan K. Genetic validation of a therapeutic target in a mouse model of ALS. Sci Transl Med. 2014;6(248):248ra104. doi:10.1126/scitranslmed.3009351

Testing the accuracy of an observation-based classifier for rapid detection of autism risk.

Duda M, Kosmicki JA, Wall DP. Testing the accuracy of an observation-based classifier for rapid detection of autism risk. Transl Psychiatry. 2014;4:e424. doi:10.1038/tp.2014.65

ProtocolNavigator: emulation-based software for the design, documentation and reproduction biological experiments.

Khan IA, Fraser A, Bray MA, et al. ProtocolNavigator: emulation-based software for the design, documentation and reproduction biological experiments. Bioinformatics. 2014;30(23):3440-2. doi:10.1093/bioinformatics/btu554

A novel common variant in DCST2 is associated with length in early life and height in adulthood.

van der Valk RJP, Kreiner-Møller E, Kooijman MN, et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum Mol Genet. 2015;24(4):1155-68. doi:10.1093/hmg/ddu510

Comprehensive variation discovery in single human genomes.

Weisenfeld NI, Yin S, Sharpe T, et al. Comprehensive variation discovery in single human genomes. Nat Genet. 2014;46(12):1350-5. doi:10.1038/ng.3121

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

Benyamin B, Esko T, Ried JS, et al. Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nat Commun. 2014;5:4926. doi:10.1038/ncomms5926