TY - JOUR
T1 - Family-based association tests for sequence data, and comparisons with population-based association tests
AU - Ionita-Laza, Iuliana
AU - Lee, Seunggeun
AU - Makarov, Vladimir
AU - Buxbaum, Joseph D.
AU - Lin, Xihong
N1 - Funding Information:
The research was partially supported by National Science Foundation grant DMS-1100279 and National Institutes of Health grants R01MH095797 and 1R03HG005908 (to II-L), a Seaver Foundation grant and National Institutes of Health grants MH089025 (to JDB) and National Institutes of Health grants R37 CA076404 and P01CA134294 (to SL and XL).
PY - 2013/10
Y1 - 2013/10
N2 - Recent advances in high-throughput sequencing technologies make it increasingly more efficient to sequence large cohorts for many complex traits. We discuss here a class of sequence-based association tests for family-based designs that corresponds naturally to previously proposed population-based tests, including the classical Burden and variance-component tests. This framework allows for a direct comparison between the powers of sequence-based association tests with family- vs population-based designs. We show that for dichotomous traits using family-based controls results in similar power levels as the population-based design (although at an increased sequencing cost for the family-based design), while for continuous traits (in random samples, no ascertainment) the population-based design can be substantially more powerful. A possible disadvantage of population-based designs is that they can lead to increased false-positive rates in the presence of population stratification, while the family-based designs are robust to population stratification. We show also an application to a small exome-sequencing family-based study on autism spectrum disorders. The tests are implemented in publicly available software.
AB - Recent advances in high-throughput sequencing technologies make it increasingly more efficient to sequence large cohorts for many complex traits. We discuss here a class of sequence-based association tests for family-based designs that corresponds naturally to previously proposed population-based tests, including the classical Burden and variance-component tests. This framework allows for a direct comparison between the powers of sequence-based association tests with family- vs population-based designs. We show that for dichotomous traits using family-based controls results in similar power levels as the population-based design (although at an increased sequencing cost for the family-based design), while for continuous traits (in random samples, no ascertainment) the population-based design can be substantially more powerful. A possible disadvantage of population-based designs is that they can lead to increased false-positive rates in the presence of population stratification, while the family-based designs are robust to population stratification. We show also an application to a small exome-sequencing family-based study on autism spectrum disorders. The tests are implemented in publicly available software.
KW - burden and variance-component tests
KW - family-and population-based association tests
KW - sequence data
UR - https://www.scopus.com/pages/publications/84884595534
U2 - 10.1038/ejhg.2012.308
DO - 10.1038/ejhg.2012.308
M3 - Article
C2 - 23386037
AN - SCOPUS:84884595534
SN - 1018-4813
VL - 21
SP - 1158
EP - 1162
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 10
ER -