Neanderthal Genomics Suggests a Pleistocene Time Frame for the First Epidemiologic Transition

Neanderthal Genomics Suggests a Pleistocene Time Frame for the First Epidemiologic Transition

Charlotte Jane Houldcroft , Simon Underdown
doi: http://dx.doi.org/10.1101/017343

High quality Altai Neanderthal and Denisovan genomes are revealing which regions of archaic hominin DNA have persisted in the modern human genome. A number of these regions are associated with response to infection and immunity, with a suggestion that derived Neanderthal alleles found in modern Europeans and East Asians may be associated with autoimmunity. Independent sources of DNA-based evidence allow a re-evaluation of the nature and timing of the first epidemiologic transition. By combining skeletal, archaeological and genetic evidence we question whether the first epidemiologic transition in Eurasia was as tightly tied to the onset of the Holocene as has previously been assumed. There is clear evidence to suggest that this transition began before the appearance of agriculture and occurred over a timescale of tens of thousands of years. The transfer of pathogens between human species may also have played a role in the extinction of the Neanderthals.

XWAS: a software toolset for genetic data analysis and association studies of the X chromosome

XWAS: a software toolset for genetic data analysis and association studies of the X chromosome

Feng Gao , Diana Chang , Arjun Biddanda , Li Ma , Yingjie Guo , Zilu Zhou , Alon Keinan
doi: http://dx.doi.org/10.1101/009795

XWAS is a new software for the analysis of the X chromosome in association studies and similar studies. The X chromosome plays an important role in human disease, especially those with sexually dimorphic characteristics. Special attention needs to be given to its analysis due to the unique inheritance pattern, leading to analytical complications that have resulted in the majority of genome-wide association studies (GWAS) either not considering X or mishandling it with GWAS toolsets that have been designed for non-sex chromosomes.. Hence, XWAS fills the need for tools that are specially designed for analysis of X. Following extensive, stringent, and X-specific quality control, XWAS offers an array of statistical tests of association, including: (1) the standard test between a SNP (single nucleotide polymorphism) and disease risk, including after first stratifying individuals by sex, (2) a test for a differential effect of a SNP on disease between males and females, (3) motivated by X-inactivation, a test for higher variance of a trait in heterozygous females as compared to homozygous females, and (4) for all tests, a version that allows for combining evidence across all SNPs in a whole gene. We applied the toolset analysis pipeline to 16 GWAS datasets of immune-related disorders and to 7 risk factors of coronary artery disease, and discovered several new X-linked genetic associations. XWAS will provide the tools and incentive for others to incorporate the X chromosome into GWAS, hence enabling discoveries of novel loci implicated in many diseases and in their sexual dimorphism.

Most viewed on Haldane’s Sieve: March 2015

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