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1,228 bytes added ,  10:34, 21 February 2017
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* Source code can be downloaded in the following
 
* Source code can be downloaded in the following
 
   
 
   
   [[Media:LINUX_famrvtest.2.2.tgz|Source for '''LINUX''']]
+
   [[Media:LINUX_famrvtest.2.4.tgz|Source for '''LINUX''']]
   [[Media:MAC_famrvtest.2.2.tgz|Source for '''MAC''']]
+
   [[Media:MAC_famrvtest.2.4.tgz|Source for '''MAC''']]
   [[Media:MINGW_famrvtest.2.2.tgz|Source for '''MINGW''']]
+
   [[Media:MINGW_famrvtest.2.4.tgz|Source for '''MINGW''']]
   [[Media:CYGWIN64_famrvtest.2.2.tgz|Source for '''CYGWIN64''']]
+
   [[Media:CYGWIN64_famrvtest.2.4.tgz|Source for '''CYGWIN64''']]
    
* Executable can be downloaded in the following:
 
* Executable can be downloaded in the following:
   −
   [[Media:Linux_binary.tar.gz |Executable for '''LINUX''']]
+
   [[Media:Famrvtest.2.4.linux.executable.tgz |Executable for '''LINUX''']]
    
=== How to Compile ===
 
=== How to Compile ===
 
* Save it to your local path and decompress using the following command:
 
* Save it to your local path and decompress using the following command:
   tar xvzf Linux_famRvTest.2.2.tgz
+
   tar xvzf LINUX_famrvtest.2.4.tgz
 
* Go to promp>famrvtest and type the following command to compile:
 
* Go to promp>famrvtest and type the following command to compile:
   make -j 5
+
   make
    
=== How to Execute ===
 
=== How to Execute ===
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=== PED and DAT Files ===
 
=== PED and DAT Files ===
 
* When PED file has genotypes saved, there is no need for a VCF file as input.
 
* When PED file has genotypes saved, there is no need for a VCF file as input.
* '''famrvtest''' takes PED/DAT file in [http://www.sph.umich.edu/csg/abecasis/Merlin/index.html|'''Merlin'''] format. Please refer to [http://www.sph.umich.edu/csg/abecasis/merlin/tour/input_files.html PED/DAT format description] for details.
+
* '''famrvtest''' takes PED/DAT file in [http://www.sph.umich.edu/csg/abecasis/Merlin/index.html '''Merlin'''] format. Please refer to [http://sph.umich.edu/csg/abecasis/merlin/tour/input_files.html PED/DAT format description] for details.
 
* An example PED file is in the following:
 
* An example PED file is in the following:
 
     1 1 0 0 1 1.5 1 23 A A A A A A A A A A
 
     1 1 0 0 1 1.5 1 23 A A A A A A A A A A
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   tabix -p vcf -f input.vcf.gz  ## this command will generate input.vcf.gz.tbi
 
   tabix -p vcf -f input.vcf.gz  ## this command will generate input.vcf.gz.tbi
 
* Even with the presence of VCF file, PED/DAT files are still needed for covariates and phenotypes.
 
* Even with the presence of VCF file, PED/DAT files are still needed for covariates and phenotypes.
 +
 +
=== Group File for Gene-level Tests===
 +
* Grouping methods are only necessary for gene-level tests.
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* With --groupFile option, you can specify particular set of variants to be grouped for burden tests.
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* The group file must be a tab or space delimited file in the following format:
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  GROUP_ID MARKER1_ID MARKER2_ID MARKER3_ID ...
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* MARKER_ID must be in the following format:
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  CHR:POS:ALLELE1:ALLELE2
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* An example group file is:
 +
  PLEKHN1 1:901922:G:A    1:901923:C:A    1:902088:G:A    1:902128:C:T    1:902133:C:G    1:902176:C:T    1:905669:C:G       
 +
  HES4    1:934735:A:C    1:934770:G:A    1:934801:C:T    1:935085:G:A    1:935089:C:G
 +
* '''Version 2.4 and later allow variants from different chromosomes to be grouped for testing. This might be useful for pathway analysis.'''
 +
* '''Note: any variants that have different alleles from listed in group file will be excluded from gene-level tests.'''
    
== Example Command Line ==
 
== Example Command Line ==
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* Released version 2.0, a faster version and added family-based single variant permutation test. (7/14/2014)
 
* Released version 2.0, a faster version and added family-based single variant permutation test. (7/14/2014)
 
* Released version 2.2, a bug fixed which causes single variant test can not be run alone. (7/15/2014)
 
* Released version 2.2, a bug fixed which causes single variant test can not be run alone. (7/15/2014)
 +
* Uploaded new source code package for version2.2, with updated makefiles. (8/4/14)
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* Released version 2.3. Fixed a bug which causes compiling error (not finding the correct makefile). (8/20/14)
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* Released version 2.4. Enable analyzing pathways where variants from different chromosomes can be grouped. (9/27/2014)
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