487
edits
Changes
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Added --allTypedVariants option which adds variants which were
Added --allTypedVariants option which adds variants which were
typed ONLY to the imputed output files and imputes any missing
values in such variants to the MAF. Also fixed a bug with chr-
-omosome X only male samples. Also added --rsid option to use
rs IDs of variants.
rs IDs of variants.
==Ver 1.0.12 (April 21, 2015)==
==Ver 1.0.11 (April 21, 2015)==
Version : 1.0.11
Version : 1.0.11
Implemented parallel threading for processReference. Moved all
Implemented parallel threading for processReference. Moved all
haplotype data from char vector to bool vector. Implemented
David's patch and similar other division-removal techniques.
Also added legacy parameter unphased for unphased output.
==Ver 1.0.10 (February 27, 2015)==
==Ver 1.0.10 (February 27, 2015)==
