Difference between revisions of "BEAGLE"
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{{#if: {{#var: citation}}|==Citation== | {{#if: {{#var: citation}}|==Citation== | ||
If you use BEAGLE in a published analysis, please report the BEAGLE version used and cite the appropriate publication or publications listed below. | If you use BEAGLE in a published analysis, please report the BEAGLE version used and cite the appropriate publication or publications listed below. | ||
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BEAGLE's fastIBD method is described in | BEAGLE's fastIBD method is described in | ||
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* S R Browning (2006) Multilocus association mapping using variable-length Markov chains. Am J Hum Genet 78:903-13. | * S R Browning (2006) Multilocus association mapping using variable-length Markov chains. Am J Hum Genet 78:903-13. | ||
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Latest revision as of 15:36, 14 December 2022
Description
BEAGLE is a state of the art software package for analysis of large-scale genetic data sets with hundreds of thousands of markers genotyped on thousands of samples. BEAGLE can
- phase genotype data (i.e. infer haplotypes) for unrelated individuals, parent-offspring pairs, and parent-offspring trios.
- infer sporadic missing genotype data.
- impute ungenotyped markers that have been genotyped in a reference panel.
- perform single marker and haplotypic association analysis.
- detect genetic regions that are homozygous-by-descent in an individual or identical-by-descent in pairs of individuals.
Environment Modules
Run module spider Beagle to find out what environment modules are available for this application.
System Variables
- HPC_BEAGLE_DIR - installation directory
- HPC_BEAGLE_BIN
- HPC_BEAGLE_DOC
- HPC_BEAGLE_EXAMPLE
Citation
If you use BEAGLE in a published analysis, please report the BEAGLE version used and cite the appropriate publication or publications listed below.
Expand this section to view citation instructions.
BEAGLE's fastIBD method is described in
- B L Browning and S R Browning (2011) A fast, powerful method for detecting identity by descent. The American Journal of Human Genetics 88:173-182.
BEAGLE's methods for detecting homozygosity-by-descent and identity-by-descent are described in
- S R Browning and B L Browning (2010) High-resolution detection of identity by descent in unrelated individuals. The American Journal of Human Genetics 86:526-539. [link to article]
BEAGLE's methods for calling genotypes from genotype likelihood data are described in
- B L Browning and Z Yu (2009) Simultaneous genotype calling and haplotype phase inference improves genotype accuracy and reduces false positive associations for genome-wide association studies. The American Journal of Human Genetics 85:847-861.
BEAGLE's methods for imputing ungenotyped markers and phasing parent-offspring trios are described in
- B L Browning and S R Browning (2009) A unified approach to genotype imputation and haplotype phase inference for large data sets of trios and unrelated individuals. Am J Hum Genet 84:210-223.
BEAGLE's methods for inferring haplotype phase or sporadic missing data in unrelated individuals are described in
- S R Browning and B L Browning (2007) Rapid and accurate haplotype phasing and missing data inference for whole genome association studies using localized haplotype clustering. Am J Hum Genet 81:1084-1097.
BEAGLE's methods for association testing are described in
- B L Browning and S R Browning (2007) Efficient multilocus association mapping for whole genome association studies using localized haplotype clustering. Genet Epidemiol 31:365-375.
BEAGLE's haplotype frequency model was first described in:
- S R Browning (2006) Multilocus association mapping using variable-length Markov chains. Am J Hum Genet 78:903-13.