FamLDCaller specifications


Unique identifier OMICS_11038
Name FamLDCaller
Software type Application/Script
Interface Command line interface
Restrictions to use None
Input data The input files are simply a vcf file that includes genotype likelihood (or in phred-scale) and a pedigree file that includes relativeness information among individuals.
Operating system Unix/Linux
Programming languages C++
Computer skills Advanced
Stability Stable
Maintained Yes


No version available


  • person_outline Wei Chen

Publication for FamLDCaller

FamLDCaller institution(s)
Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, MD, USA; Department of Molecular Physiology & Biophysics, Vanderbilt University Medical Center, Nashville, TN, USA; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA; Department of Psychology & Neuroscience, Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA; Department of Psychology, University of Minnesota, Minneapolis, MN, USA; Division of Pulmonary Medicine, Allergy and Immunology, Children’s Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA
FamLDCaller funding source(s)
This study is supported by the research grants R01HG007358, R01HG006857 and R01DA024417 from National Institute of Health.

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