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Human Mutation|June 21, 2006
A quality assessment survey of SNP genotyping laboratoriesPäivi Lahermo, Ulrika Liljedahl, Grethe Alnaes, et al.European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.Genome Research|March 7, 2009
Geographical structure and differential natural selection among North European populationsBrian P McEvoy, Grant W Montgomery, Allan F McRae, et al.Plos One|January 10, 2013
Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expressionJonas Carlsson Almlöf, Per Lundmark, Anders Lundmark, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 4, 2012
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterolIda Surakka, John B Whitfield, Markus Perola, et al.Scientific Data|November 10, 2021
Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark studyYongmei Zhao, Li Tai Fang, Tsai-Wei Shen, et al.Genome Biology|December 7, 2021
The SEQC2 epigenomics quality control (EpiQC) studyJonathan Foox, Jessica Nordlund, Claudia Lalancette, et al.Nature Biotechnology|September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencingLi Tai Fang, Bin Zhu, Yongmei Zhao, et al.Nature Biotechnology|September 10, 2021
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencingWenming Xiao, Luyao Ren, Zhong Chen, et al.Science (New York, N.Y.)|October 9, 2025
A human pan-disease blood atlas of the circulating proteomeMaría Bueno Álvez, Sofia Bergström, Josefin Kenrick, et al.Pageof 4