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1 Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads [期刊论文]

来源：BMC Genomics

作者:Wen Fury;Yi Wei;Blerta Cooper;等

关键词:Human genetics;Immunoncology;...

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2 Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads [期刊论文]

来源：BMC Genomics

作者:Wen Fury;Yi Wei;Blerta Cooper;等

关键词:Human genetics;Immunoncology;...

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3 Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency [期刊论文]

来源：BMC Medical Genetics

作者:Vamsi K Mootha;Jeremy D Schmahmann;Katherine B Sims;等

关键词:Peroxisomal defects;Multi-system disorders;...

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4 Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency [期刊论文]

来源：BMC Medical Genetics

作者:Vamsi K Mootha;Jeremy D Schmahmann;Katherine B Sims;等

关键词:Peroxisomal defects;Multi-system disorders;...

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5 Loss of heterozygosity in tumor cells requires re‐evaluation: the data are biased by the size‐dependent differential sensitivity of allele detection [期刊论文]

来源：FEBS Letters , 1999

作者:Klein, George;Zabarovska, Veronika I.;Alimov, Andrei;等

关键词:Human genetics;Loss of heterozygosity;...

使用许可:Unknown

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6 Impact of Bacterial and Human Genetic Variation on Staphylococcus aureus Infections [期刊论文]

来源：PLOS Pathogens , 2016

作者:Batu K. Sharma-Kuinkel;Vance G. Fowler Jr.;Julia A. Messina;等

关键词:Staphylococcus aureus;Staphylococcal infection;...

使用许可:Unknown

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