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.
Saturday, October 24, 2009
A new primate phylogeny
Where's the ecology in molecular ecology?
Monday, October 19, 2009
Two Main Bottleneck Events Shaped Modern Human Genetic Diversity
Humans are widely thought to have expanded out Africa starting approximately 50,000 years ago. In this process, genetic variation was reduced the further populations moved away from Africa due to successive bottleneck events. The frequency and nature of these bottleneck events have already been extensively explored in the literature. A recent study, which analyzed 783 microsatellite loci genotyped on 53 globally representative populations, concludes that two major bottleneck events occurred in human history – the first occurring as humans moved out of Africa and the second as humans moved across the Bering Strait into the New World. These events can be detected due to the genetic implications of bottleneck events. After sharp declines in population numbers, excess heterozygosity exists in the population than would be expected given the number of alleles remaining. The authors used the program ‘Bottleneck’ to detect this signature. This study reconfirms the conventional understanding of human expansion.
Sunday, October 18, 2009
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Monday, October 5, 2009
Mutations in LOXHD1...distrupt hair cell function, cause progressive hearing loss
Sunday, October 4, 2009
Aging is RSKy Business
Thursday, October 1, 2009
Ardipithecus ramidus
Sunday, September 27, 2009
Kipunji Monkeys
There's no looking back (evolutionarily speaking)
Variance in mtDNA Among Bantu-speaking Populations
Friday, September 25, 2009
For all you Callithrix jacchus fans out there...
Wednesday, September 23, 2009
Reconstructing Indian population history
Tuesday, September 22, 2009
. . . not genetics but important to everyone that studies primates :)
Wednesday, September 16, 2009
HuGE Navigator
Sunday, September 13, 2009
recent positive selection on genes associated with/linked to male pattern baldness
Interestingly, it is the AGA risk haplotype that
shows evidence for positive selection in the European
population. The AGA risk haplotype also carries a derived
non-synonymous allele (57K) in the flanking ectodysplasin
A2 receptor gene (EDA2R). The 57K allele may have been
the target of positive selection in East Asians: it shows
large allele frequency diverences between populations,
lies in a likely functional domain of the
EDA2R protein, and the ancestral allele, 57R, is conserved
from human to rat. Thus, the AGA risk haplotype may have
hitchhiked to high frequency in Europeans as a result of
positive selection on the linked 57K allele in EDA2R
Tuesday, September 8, 2009
Where Did All the Flowers Come From? Flower Genomics
Thursday, September 3, 2009
Recent de novo origin of human protein-coding genes
Fossil feather coloration
http://www.nature.com/nature/journal/v461/n7260/full/461014c.html
Saturday, August 29, 2009
more interesting candidate genes: size, longevity, behavioral stereotypes
Friday, August 28, 2009
adaptive coloration in deer mice
Thursday, August 27, 2009
Linus Pauling quote
genetics of dog hair (length and curl)
Friday, August 21, 2009
hamadryas genome
Thursday, August 20, 2009
DNA from difficult samples
Wednesday, August 19, 2009
sleep genes
Link's don't work?
Times story:
http://well.blogs.nytimes.com/2009/08/06/the-pain-of-being-a-redhead/
Study page:
http://jada.ada.org/cgi/content/abstract/140/7/896