Tuesday, December 8, 2009
Thursday, November 19, 2009
Kipungi Hybridization Revisited
Tuesday, November 10, 2009
A common variation in EDAR is a genetic determinant of shovel-shaped incisors
Global Microsatellite Content Distiguishes Humans, Primates, Animals and Plants
Targets of Balancing Selection in the Human Genome
Sunday, October 25, 2009
Heritability and Demographic Analyses in the Large Isolated Population of Val Borbera Suggest Advantages in Mapping Complex Traits Genes
Genetic studies performed on heterogeneous populations make identifying rare variants for complex diseases difficult because of confounding variables associated with heterogeneous populations. This study collected genetic samples and medical information for 1803 people within a relatively isolated population. The authors report that analysis of the isolated population reveals significant heritability of medically relevant traits that might not have otherwise been uncovered with a more heterogeneous cohort.
Human DNA methylomes at base resolution show widespread epigenomic differences
Human genetic variation extends beyond differences in the underlying genetic sequence. A recent study reported in Nature provides a more robust understanding of DNA cytosine methylation, an alternate source of genetic variation. While DNA methylation was primarily associated with repeat CpG (Cytosine-phosphate-Guanine) rich portions of the genome, Lister et al. report that approximately 25% of methylation in embryonic stem cells occurs in non CpG portions of the genomes. CpG regions are associated with promoter regions of genes, and methylation of these regions are thought to regulate gene expression. The report of methylation in non CpG regions raises new questions about the role of this epigenetic modification. The publication also represents one of the first papers describing a relatively complete map of the human epigenome.