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First you want to know what is in the vcf file.
 
First you want to know what is in the vcf file.
   −
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz
    
   stats: no. of samples                    :        62
 
   stats: no. of samples                    :        62
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We can count the number of variants with different filters with the following commands.
 
We can count the number of variants with different filters with the following commands.
   −
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.PASS"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.PASS"
    
   stats: no. of samples                    :        62
 
   stats: no. of samples                    :        62
 
         no. of chromosomes                :          1 <br>
 
         no. of chromosomes                :          1 <br>
         no. Indels                        :        584
+
         no. Indels                        :        583
             2 alleles (ins/del)            :            584 (0.69) [239/345]
+
             2 alleles (ins/del)            :            583 (0.69) [239/344]
 
             >=3 alleles (ins/del)          :              0 (-nan) [0/0]
 
             >=3 alleles (ins/del)          :              0 (-nan) [0/0]
   −
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.overlap"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.overlap"
    
   stats: no. of samples                    :        62
 
   stats: no. of samples                    :        62
 
         no. of chromosomes                :          1 <br>
 
         no. of chromosomes                :          1 <br>
         no. Indels                        :        136
+
         no. Indels                        :        137
             2 alleles (ins/del)            :            136 (1.89) [89/47]  #notice the difference in insertion deletion ratios
+
             2 alleles (ins/del)            :            137 (1.85) [89/48]  #notice the difference in insertion deletion ratios
 
             >=3 alleles (ins/del)          :              0 (-nan) [0/0]
 
             >=3 alleles (ins/del)          :              0 (-nan) [0/0]
    
   #passed singletons only
 
   #passed singletons only
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.PASS&&INFO.AC==1"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.PASS&&INFO.AC==1"
 
   
 
   
 
   #passed indels of length 1 only
 
   #passed indels of length 1 only
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.PASS&&LEN==1"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.PASS&&LEN==1"
 
   
 
   
 
   #passed indels of length >4  
 
   #passed indels of length >4  
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.PASS&&LEN>4"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.PASS&&LEN>4"
 
    
 
    
 
   #passed singletons of length 4 or insertions of length 3
 
   #passed singletons of length 4 or insertions of length 3
   ${GC}/bin/vt peek ${OUT}/final/all.genotypes.vcf.gz -f "FILTER.PASS&&(LEN==4||DLEN==3)"
+
   ${GC}/bin/vt peek ${OUT}/indel/final/all.genotypes.vcf.gz -f "FILTER.PASS&&(LEN==4||DLEN==3)"
    
=== Comparison with other data sets ===
 
=== Comparison with other data sets ===

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