FamLinkX – implementation of a general model for likelihood computations for X-chromosomal marker data
Author:
Publisher
Elsevier BV
Subject
Genetics,Pathology and Forensic Medicine
Reference23 articles.
1. Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome;Nothnagel;Forensic Sci. Int. Genet.,2012
2. Population genetic analysis of 12 X-STRs in Swedish population;Tillmar;Forensic Sci. Int. Genet.,2012
3. Using X-chromosomal markers in relationship testing: calculation of likelihood ratios taking both linkage and linkage disequilibrium into account;Tillmar;Forensic Sci. Int. Genet.,2010
4. X-chromosomal haplotype frequencies of four linkage groups using the Investigator Argus X-12 Kit;Edelmann;Forensic Sci. Int. Genet.,2012
5. X-chromosome markers in kinship testing: a generalisation of the IBD approach identifying situations where their contribution is crucial;Pinto;Forensic Sci. Int. Genet.,2011
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