Karyn Steinberg, Ph.D.

Genome Sciences University of Washington, Seattle, Seattle, WA 
"Karyn Steinberg"
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Huddleston J, Chaisson MJP, Steinberg KM, et al. (2018) Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data. Genome Research. 28: 144
Schneider VA, Graves-Lindsay T, Howe K, et al. (2017) Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. Genome Research
Huddleston J, Chaisson MJ, Meltz Steinberg K, et al. (2016) Discovery and genotyping of structural variation from long-read haploid genome sequence data. Genome Research
Steinberg KM, Yu B, Koboldt DC, et al. (2015) Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. Scientific Reports. 5: 9124
Leslie EJ, Taub MA, Liu H, et al. (2015) Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American Journal of Human Genetics. 96: 397-411
Church DM, Schneider VA, Steinberg KM, et al. (2015) Extending reference assembly models. Genome Biology. 16: 13
Watson CT, Steinberg KM, Graves TA, et al. (2015) Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity. Genes and Immunity. 16: 24-34
Steinberg KM, Schneider VA, Graves-Lindsay TA, et al. (2014) Single haplotype assembly of the human genome from a hydatidiform mole. Genome Research. 24: 2066-76
Antonacci F, Dennis MY, Huddleston J, et al. (2014) Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability. Nature Genetics. 46: 1293-302
Koboldt DC, Larson DE, Sullivan LS, et al. (2014) Exome-based mapping and variant prioritization for inherited Mendelian disorders. American Journal of Human Genetics. 94: 373-84
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