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Haploxt (view source)

Revision as of 18:22, 21 October 2010

172 bytes removed ,  18:22, 21 October 2010
→‎--r2Threshold or -t
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haploxt is a C/C++ software developed by [https://www.sph.umich.edu/csg/yli/ Yun Li] and [https://www.sph.umich.edu/csg/abecasis/ Goncalo Abecasis]. It calculates LD (D' and r<sup>2</sup>) from phased haplotypes.  
 
haploxt is a C/C++ software developed by [https://www.sph.umich.edu/csg/yli/ Yun Li] and [https://www.sph.umich.edu/csg/abecasis/ Goncalo Abecasis]. It calculates LD (D' and r<sup>2</sup>) from phased haplotypes.  
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= Options =
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= Input Files =
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== --impped --impdat <br>  ==
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== Required Input ==
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specify one input pedigree set.
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=== Haplotype File  ===
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== --trueped --truedat <br> ==
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Fed to the option --haps or -h, the input haplotype file is in the form of one haplotype per line (no delimiter between alleles). The file could contain fields other than the actual haplotypes but must proceed the actual haplotype field. Allele coding is flexible: accepted coding includes 1234, ACGT, 12, AB etc. <br><br>  
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specify the other input pedigree set.
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Sample haplotype file 1:<br>
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Indiv1 HAPLO1 142344111132344413444421333122313342113321324233112323134222<br>
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Indiv1 HAPLO2 144222444221443323334431431242131234311333144223411321334422<br>
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Indiv2 HAPLO1 144224441221443323334331431243131232311321123323432321334412<br>
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Indiv2 HAPLO2 342222444221344312343433333122313344113321324223112323334412<br>
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== --match  ==
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Sample haplotype file 2:<br>
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142344111132344413444421333122313342113321324233112323134222<br>
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144222444221443323334431431242131234311333144223411321334422<br>
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144224441221443323334331431243131232311321123323432321334412<br>
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342222444221344312343433333122313344113321324223112323334412<br>
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generates a matrix taking values 0,1,2 indicating # of matched alleles. The dimension of the matrix is # of overlapping individuals times # of overlapping markers of the two input pedigree sets.
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=== SNP File ===
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== --bySNP  ==
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Fed to the option --snps or -s, the input SNP file is a list of SNP name in the same order as in the haplotype file. One SNP per line. <br> <br>
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is turned on by default to generate SNP specific measures. The output .bySNP will contain the following 6 fields for each SNP:
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Sample SNP file: <br>
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SNP1<br>
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SNP2<br>
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SNP3<br>
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...<br> <br>
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    (1) SNP&nbsp;: SNP name
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== Optional Input ==
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  (2) gErr&nbsp;: genotypic discordance rate
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=== Relevant SNP File ===
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  (3) aErr&nbsp;: allelic discordance rate
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Fed to the option --relevant or -r, the relevant SNP file is a list of SNPs among which LD values are desired.
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  (4) matchedG&nbsp;: number of genotypes matched
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  (5) matchedA: number of alleles matched
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  (6) maskedG: total number of genotypes evaluated/masked (&lt;=n of course) (I should change the naming to comparedG or evaluatedG)
     −
<br>  
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= Options =
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== --allelefrequency ==
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Option to calculate allele frequency and output to prefix.freq. <br>
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== --byGeno  ==
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== --allelecounts ==
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Option to calculate allele counts and output to prefix.ac. <br>
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can be added on top of --bySNP. It will generates the following fields after the 6 fields above:
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== --ld ==
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Option to calculate LD. Note that this option has to be turned on for LD to be calculated. <br>
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    (7) hetAerr&nbsp;: allelic discordance rate among heterozygotes
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== --windowSize or -w ==
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  (8) AL1: allele 1 (an arbitrary allele)
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Option to specify the # of flanking SNPs with which LD values are calculated for each SNP. Default is 1,000, meaning that LD with 1,000 SNPs on each side (2,000 total) will be calculated for each SNP. <br>
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  (9) AL2: allele 2
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  (10) freq1: frequency of AL1
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  (11) MAF
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  (12) #true 1/1: # individuals with experimental genotype AL1/AL1
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  (13) mm1/2: # of true AL1/AL1 being imputed as AL1/AL2
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  (14) mm2/2: # of true AL1/AL1 being imputed as AL2/AL2
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  (15) #true 1/2
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  (16) mm1/1
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  (17) mm2/2
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  (18) #true 2/2
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  (19) mm1/1
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  (20) mm1/2
     −
<br>  
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== --r2Threshold or -t ==
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Minimum r<sup>2</sup> value for a pair of SNPs to be in output. Default is 0.00. <br>
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<br>  
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== --DprimeThreshold or -d ==
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Minimum D' value for a pair of SNPs to be in output. Default is 0.00. <br>
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== --accuracyByGeno  ==
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== --pairWithSNP ==
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Option to calcuate LD only with a particular SNP. <br>
   −
Similar to --byGeno, it is used on top of --bySNP. It may be used together with --byGeno. It will generate the following fields, after (7-20) is --byGeno is turned on or after the 6th field otherwise.  
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== --pairWithList ==
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A list of SNPs with which LD values will be calculated. <br>
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    (A) almajor: major allele
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== --coupling ==
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  (B) alminor: minor allele
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Option to output for each pair the alleles that are positively correlated. <br>
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  (C) freq1: major allele frequency
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  (D) accuracy11: allelic concordance rate for homozygotes major allele
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  (E) accuracy12: allelic concordance rate for heterozygotes
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  (F) accuracy22: allelic concordance rate for homozygotes minor allele
     −
<br>  
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== --prefix or -o ==
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Option to specify output prefix. <br>
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== --byPerson  ==
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= Output =
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== .freq ==
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Generated when option --allelefrequency is turned on. <br> <br>
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generates a separate output file .byPerson and contains the following information for each person:  
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sample.freq <br>
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SNP AL1 AL2 Freq1 MAF<br>
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chr12:16099 1 3 0.4000 0.4000<br>
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chr12:16163 4 2 0.9000 0.1000<br>
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rs7358779 2 3 0.1000 0.1000<br>
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chr12:17063 1 3 0.8000 0.2000<br>
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...<br>
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<br>
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    (1) famid
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== .ac ==
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  (2) subjID
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Generated when option --allelecounts is turned on. <br> <br>
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  (3) gErr
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  (4) aErr
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  (5) matchedG
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  (6) matchedA
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  (7) maskedG
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<br> This --byPerson option is useful if there is potential sample swap or inter-individual difference, e.g., sequencing depth, number of markers genotyped.
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sample.ac<br>
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SNP AL1 AL2 AC1 MAC<br>
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chr12:16099 1 3 4 4<br>
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chr12:16163 4 2 9 1<br>
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rs7358779 2 3 1 1<br>
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chr12:17063 1 3 8 2<br>
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<br>
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<br>  
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== .xt ==
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Generated when option --ld is turned on. <br> <br>
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== --maskflag --maskped --maskdat  ==
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sample.xt<br>
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M1 M2 DPRIME DELTASQ COUPLING<br>
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chr12:16252 chr12:16585 1.0000 0.6667 2,1<br>
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chr12:16252 chr12:16665 1.0000 1.0000 2,3<br>
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chr12:16252 chr12:16693 1.0000 1.0000 2,4<br>
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...<br>
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<br>
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CalcMatch compares all genotypes overlapping the two input sets. However, when --maskflag is turned on AND --maskped and --maskdat are specified (I know ...) it compares only the following subset of the overlapping genotypes: genotypes either not found (i.e., individual or marker not included) or missing (included but with value 0/0, N/N, ./. etc) in --maskped / --maskdat. These options are useful when some individuals were masked for some SNPs while others masked for a different set of SNPs.  
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= download =
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You can download the source codes and example files [https://www.sph.umich.edu/csg/yli/haploxt_V108.tgz haploxt].
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= example command lines  =
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To install, simply type the following command:
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   CalcMatch --trueped true.ped --truedat true.dat --impped imp.ped --impdat imp.dat -o CalcMatch.Output --byPerson
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   ./build.csh
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Will generate CalcMatch.Output.bySNP (6 fields only) and CalcMatch.Output.byPerson.
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= sample command line =
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   CalcMatch --trueped true.ped --truedat true.dat --impped imp.ped --impdat imp.dat -o CalcMatch.Output --byGeno --byPerson
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   ./haploxt_names -s sample.snps -h sample.hap --allelefreq --ld -w 500 -t 0.5 --coupling -o sample.out
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Will generate CalcMatch.Output.bySNP (6+20 fields) and CalcMatch.Output.byPerson.
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= Additional Questions =
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Please email [mailto:yunli@med.unc.edu Yun Li].
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  CalcMatch --trueped true.ped --truedat true.dat --impped imp.ped --impdat imp.dat -o CalcMatch.Output --accuracyByGeno --byPerson
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Will generate CalcMatch.Output.bySNP (6+6 fields only) and CalcMatch.Output.byPerson.
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  CalcMatch --trueped true.ped --truedat true.dat --impped imp.ped --impdat imp.dat -o CalcMatch.Output --accuracyByGeno --byGeno --byPerson
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Will generate CalcMatch.Output.bySNP (6+20+6 fields only) and CalcMatch.Output.byPerson.
 
Ylwtx
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