Human
Genome News Archive Edition |
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Human Genome News, January-March 1996; 7(5)
MIM v1.2 implements the Multipoint IBD method (Goldgar, 1990; Goldgar and Oniki, 1992) for partitioning genetic variance of quantitative traits to specific chromosomal regions using data on nuclear families. More complex pedigrees must be decomposed into groups of nuclear families to enable use of this program. MIM allows multiple analyses from the same input file and has an enhanced error-checking routine and user-friendly file format. The program is written in C for a UNIX workstation but should be readily portable to a wide variety of computer systems. [Program copies: Edward Kort, University of Utah (edward@episun2.med.utah.ed or via ftp to morgan.med.utah.edu in the directory /pub/Mim/)]
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