v2.2.2 *--indel_alleles option now will flip negative strand for SNPs v2.1 *Added option "--indel_alleles" for using longer allele names than single character. Please note that enabling that option will remove strand flipping. *Added "Analysis finished." line to log file and standard output. v2.0.7 *Fixed a typo in printing effect directions for cohorts where p-value was 1 v2.0.6 *Fixed typos in manual and in command line options (thanks Josh!) v2.0.5 *Repaired effect allele frequency discrepancy check. will print now warning and increase strand problem quantity if eaf difference larger than 30% v2.0.4 *Repaired an issue with IMPUTED column (segmentation fault if value not 1 or 0) v2.0.4 *Removed a bug created by previous fix v2.0.3 *Repaired issue with sex-specific results in case of missing eaf v2.0.2 *Repaired issue with alternative column names - all names are converted to uppercase to remove case sensitivity v2.0.1 *Added genomic control output file *Repaired header line in case of map option is used *If using OR and confidence intervals, the std.err calculation has changed a bit - in previous version both upper and lower confidence interval were used (and average was measured), in GWAMA v.2 only the lower one is used. This might cause a slight change in results due to rounding. v2 *Added new command line options *Added sex-specific analysis framework *Fixed bug concerning numeric alleles and negaitive strands *Made program more memory efficient *Summary file info on screen while running analysis v1.4 *Added random effect correction *Log and error file names now have changable output file root ("--output" option) *PERL scripts for reformatting SNPTEST and PLINK association results to GWAMA format have been added to webpage *Added check for column count for each row of input data *Repaired directions column - it used to be mirrored v1.3.1.1 *Added automatic strand flipping if marker is not A/T nor C/G *Repaired threshold use in effect directions v1.3.1 *Changed file input format: added N column *Changed input format: added chromosome and position columns, N column *Added --map and -qt command line options *Added R scritps for plots *Added HapMap marker maps v1.3 *Changed file input format: removed imputation accuracy, chromosome and position columns. Added alternative input file format with odds ratio information. *Changed output format: removed chromosome and position columns. Added different format options *Replaced single configuration file with command line options *Improved error trapping *Replaced chi-distribution median 0.456 with 0.4549364. Value received from R using qchisq(0.5, df= 1)