Next-Generation Sequencing in Human Genetic Studies: Genome Technologies and Applications to Human Genetic Studies.
Author: Wang J1,2, Wang K3,4, Liu X5, Sham P6, Zhao Z7,8.
Comprehensive Assessment of Genotype Imputation Performance.
Author: Shi S1,2,3, Yuan N2, Yang M4, Du Z2, Wang J1,2,3, Sheng X1,2,3, Wu J1, Xiao J5,6,7.
Inferring Gene-Disease Association by an Integrative Analysis of eQTL Genome-Wide Association Study and Protein-Protein Interaction Data.
Author: Wang J1, Zheng J2, Wang Z3, Li H4,5, Deng M1,6,7.
Comparison of SureSelect and Nextera Exome Capture Performance in Single-Cell Sequencing.
Author: Huss WJ1, Hu Q2, Glenn ST3,4, Gangavarapu KJ1, Wang J2, Luce JD3, Quinn PK3, Brese EA5, Zhan F6, Conroy JM3, Paragh G7,8, Foster BA1, Morrison CD3, Liu S2, Wei L9.
英文介紹
Human Heredity雜志英文介紹
Gathering original research reports and short communications from all over the world, 'Human Heredity' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all 'Human Heredity' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.