Software-2016
Recent New Updates
FamPipe
FamPipe is an automatic analysis pipeline for analyzing sequencing data in families for disease studies. Access the pipeline at http://fampipe.sourceforge.net
To cite FamPipe, please use:
Chung RH, Tsai WY, Kang CY, Yao PJ, Tsai HJ, Chen CH. FamPipe: An automatic analysis pipeline for analyzing sequencing data in families for disease studies. PLOS Computational Biology. 2016. 12(6): e1004980.
GESDB
GESDB is a platform for sharing simulation data and discussion of simulation techniques for human genetic studies. Access the database at http://gesdb.nhri.org.tw
To cite GESDB, please use:
Yao PJ, Chung RH. GESDB: A Platform of Simulation Resources for Genetic Epidemiology Studies. Database. In press.
SeqSIMLA2_exact
SeqSIMLA2 -exact efficiently simulates genotypes conditional on disease status. Download the software from http://seqsimla.sourceforge.net
To cite SeqSIMLA2_exact, please use:
Yao PJ, Chung RH. SeqSIMLA2_exact: simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence. Bioinformatics. 2016. 32(4):557-62.
GCORE
GCORE is an efficient family-based gene-gene interaction test for trios. Download the software from http://gscore.sourceforge.net
To cite GCORE, please use:
Sung PY, Wang YT, Yu YW, Chung RH. An efficient gene-gene interaction test for genome-wide associ-ation studies in trio families. Bioinformatics. 2016. In press.
OPTPDT
OPTPDT is a family-based multi-SNP association test using an optimal p-value threshold algorithm for GWAS. Download the software from http://optpdt.sourceforge.net
To cite OPTPDT, please use:
Wang YT, Sung PY, Lin PL, Yu YW, Chung RH. 2015. A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. BMC Genomics. In Press.
OVPDT
OVPDT is a family-based association test using both common and rare variants and accounting for directions of effects for sequencing data. Download the software from http://ovpdt.sourceforge.net
To cite OVPDT, please use:
Chung RH, Tsai WY, Martin ER. 2014. Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data. PLOS ONE. 9(9):e107800
SeqSIMLA2
SeqSIMLA can simulate sequence data in families with multiple affected and unaffected siblings or unrelated case-control under different disease models. Download the software from http://seqsimla.sourceforge.net
Two disease models (the prevalence and population attributable risk models) are provided in SeqSIMLA. Alternatively, a penetrance table can be provided directly to SeqSIMLA. SeqSIMLA can also simulate quantitative traits while accounting for correlations in families.
To cite SeqSIMLA2, please use:
Chung RH, Tsai WY, Hsieh CH, Hung KY, Hsiung CA, Hauser ER. 2014. SeqSIMLA2: Simulating Correlated Quantitative Traits Accounting for Shared Environmental Effects in User-Specified Pedigree Structure. Genetic Epidemiology. In press.