File: FT.vcf

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python-pyvcf 0.6.8%2Bgit20170215.476169c-11
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##fileformat=VCFv4.2
##ALT=<ID=NON_REF,Description="Represents any possible alternative allele at this location">
##FILTER=<ID=DP125,Description="DP<125">
##FILTER=<ID=DP130,Description="DP<130">
##FILTER=<ID=LowQual,Description="Low quality">
##FILTER=<ID=Q4800,Description="QUAL<4800.0">
##FILTER=<ID=Q5000,Description="QUAL<5000.0">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads with MQ=255 or with bad mates are filtered)">
##FORMAT=<ID=FT,Number=.,Type=String,Description="Genotype-level filter">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=MIN_DP,Number=1,Type=Integer,Description="Minimum DP observed within the GVCF block">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
##FORMAT=<ID=RGQ,Number=1,Type=Integer,Description="Unconditional reference genotype confidence, encoded as a phred quality -10*log10 p(genotype call is wrong)">
##FORMAT=<ID=SB,Number=4,Type=Integer,Description="Per-sample component statistics which comprise the Fisher's Exact Test to detect strand bias.">
##GATKCommandLine.VariantFiltration=<ID=VariantFiltration,Version=3.6-0-g89b7209,Date="Wed Jul 27 09:50:44 CEST 2016",Epoch=1469605844963,CommandLineOptions="analysis_type=VariantFiltration input_file=[] showFullBamList=false read_buffer_size=null read_filter=[] disable_read_filter=[] intervals=null excludeIntervals=null interval_set_rule=UNION interval_merging=ALL interval_padding=0 reference_sequence=../ref.fasta nonDeterministicRandomSeed=false disableDithering=false maxRuntime=-1 maxRuntimeUnits=MINUTES downsampling_type=BY_SAMPLE downsample_to_fraction=null downsample_to_coverage=1000 baq=OFF baqGapOpenPenalty=40.0 refactor_NDN_cigar_string=false fix_misencoded_quality_scores=false allow_potentially_misencoded_quality_scores=false useOriginalQualities=false defaultBaseQualities=-1 performanceLog=null BQSR=null quantize_quals=0 static_quantized_quals=null round_down_quantized=false disable_indel_quals=false emit_original_quals=false preserve_qscores_less_than=6 globalQScorePrior=-1.0 validation_strictness=SILENT remove_program_records=false keep_program_records=false sample_rename_mapping_file=null unsafe=null disable_auto_index_creation_and_locking_when_reading_rods=false no_cmdline_in_header=false sites_only=false never_trim_vcf_format_field=false bcf=false bam_compression=null simplifyBAM=false disable_bam_indexing=false generate_md5=false num_threads=1 num_cpu_threads_per_data_thread=1 num_io_threads=0 monitorThreadEfficiency=false num_bam_file_handles=null read_group_black_list=null pedigree=[] pedigreeString=[] pedigreeValidationType=STRICT allow_intervals_with_unindexed_bam=false generateShadowBCF=false variant_index_type=DYNAMIC_SEEK variant_index_parameter=-1 reference_window_stop=0 phone_home= gatk_key=null tag=NA logging_level=INFO log_to_file=null help=false version=false variant=(RodBinding name=variant source=10.vcf) mask=(RodBinding name= source=UNBOUND) out=/home/redmar/tmp/example/snps/10_filt.vcf filterExpression=[QUAL<5000.0, QUAL<4800.0] filterName=[Q5000, Q4800] genotypeFilterExpression=[DP<130, DP<125] genotypeFilterName=[DP130, DP125] clusterSize=3 clusterWindowSize=0 maskExtension=0 maskName=Mask filterNotInMask=false missingValuesInExpressionsShouldEvaluateAsFailing=false invalidatePreviousFilters=false invertFilterExpression=false invertGenotypeFilterExpression=false setFilteredGtToNocall=false filter_reads_with_N_cigar=false filter_mismatching_base_and_quals=false filter_bases_not_stored=false">
##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency, for each ALT allele, in the same order as listed">
##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
##INFO=<ID=BaseQRankSum,Number=1,Type=Float,Description="Z-score from Wilcoxon rank sum test of Alt Vs. Ref base qualities">
##INFO=<ID=ClippingRankSum,Number=1,Type=Float,Description="Z-score From Wilcoxon rank sum test of Alt vs. Ref number of hard clipped bases">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth; some reads may have been filtered">
##INFO=<ID=DS,Number=0,Type=Flag,Description="Were any of the samples downsampled?">
##INFO=<ID=END,Number=1,Type=Integer,Description="Stop position of the interval">
##INFO=<ID=ExcessHet,Number=1,Type=Float,Description="Phred-scaled p-value for exact test of excess heterozygosity">
##INFO=<ID=FS,Number=1,Type=Float,Description="Phred-scaled p-value using Fisher's exact test to detect strand bias">
##INFO=<ID=HaplotypeScore,Number=1,Type=Float,Description="Consistency of the site with at most two segregating haplotypes">
##INFO=<ID=InbreedingCoeff,Number=1,Type=Float,Description="Inbreeding coefficient as estimated from the genotype likelihoods per-sample when compared against the Hardy-Weinberg expectation">
##INFO=<ID=MLEAC,Number=A,Type=Integer,Description="Maximum likelihood expectation (MLE) for the allele counts (not necessarily the same as the AC), for each ALT allele, in the same order as listed">
##INFO=<ID=MLEAF,Number=A,Type=Float,Description="Maximum likelihood expectation (MLE) for the allele frequency (not necessarily the same as the AF), for each ALT allele, in the same order as listed">
##INFO=<ID=MQ,Number=1,Type=Float,Description="RMS Mapping Quality">
##INFO=<ID=MQRankSum,Number=1,Type=Float,Description="Z-score From Wilcoxon rank sum test of Alt vs. Ref read mapping qualities">
##INFO=<ID=QD,Number=1,Type=Float,Description="Variant Confidence/Quality by Depth">
##INFO=<ID=RAW_MQ,Number=1,Type=Float,Description="Raw data for RMS Mapping Quality">
##INFO=<ID=ReadPosRankSum,Number=1,Type=Float,Description="Z-score from Wilcoxon rank sum test of Alt vs. Ref read position bias">
##INFO=<ID=SOR,Number=1,Type=Float,Description="Symmetric Odds Ratio of 2x2 contingency table to detect strand bias">
##contig=<ID=ref,length=4888768>
##reference=file://../ref.fasta
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	1	2	3	4	5
ref	63393	.	C	A	29454.60	.	AC=5;AF=1.00;AN=5;DP=719;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;QD=29.67;SOR=0.965	GT:AD:DP:GQ:PL	1:0,166:166:99:6740,0	1:0,142:142:99:5824,0	1:0,134:134:99:5616,0	1:0,122:122:99:4930,0	1:0,155:155:99:6371,0
ref	65903	.	AATTGCGCTG	A	7340.57	PASS	AC=1;AF=0.200;AN=5;DP=524;FS=0.000;MLEAC=1;MLEAF=0.200;MQ=60.00;QD=34.04;SOR=1.091	GT:AD:DP:FT:GQ:PL	1:0,164:164:PASS:99:7383,0	0:95,0:95:DP125;DP130:99:0,1800	0:88,0:88:DP125;DP130:99:0,1800	0:87,0:87:DP125;DP130:99:0,1800	0:89,0:89:DP125;DP130:99:0,1800
ref	70837	.	C	A	4711.61	Q4800;Q5000	AC=1;AF=0.200;AN=5;DP=512;FS=0.000;MLEAC=1;MLEAF=0.200;MQ=60.00;QD=27.64;SOR=0.726	GT:AD:DP:FT:GQ:PL	0:121,0:121:DP125;DP130:99:0,1800	0:95,0:95:DP125;DP130:99:0,1800	1:0,120:120:DP125;DP130:99:4745,0	0:87,0:87:DP125;DP130:99:0,1800	0:89,0:89:DP125;DP130:99:0,1800
ref	71448	.	C	T	31134.60	PASS	AC=5;AF=1.00;AN=5;BaseQRankSum=2.22;ClippingRankSum=0.00;DP=768;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;MQRankSum=0.00;QD=29.43;ReadPosRankSum=2.03;SOR=0.295	GT:AD:DP:FT:GQ:PL	1:0,147:147:PASS:99:5996,0	1:1,183:184:PASS:99:7501,0	1:0,113:113:DP125;DP130:99:4559,0	1:0,161:161:PASS:99:6436,0	1:0,163:163:PASS:99:6669,0
ref	104257	.	C	T	5521.61	PASS	AC=1;AF=0.200;AN=5;DP=506;FS=0.000;MLEAC=1;MLEAF=0.200;MQ=60.00;QD=29.45;SOR=0.854	GT:AD:DP:FT:GQ:PL	0:101,0:101:DP125;DP130:99:0,1800	0:109,0:109:DP125;DP130:99:0,1800	1:0,132:132:PASS:99:5555,0	0:67,0:67:DP125;DP130:99:0,1800	0:97,0:97:DP125;DP130:99:0,1800
ref	140658	.	C	A	32467.60	PASS	AC=5;AF=1.00;AN=5;BaseQRankSum=2.24;ClippingRankSum=0.00;DP=801;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;MQRankSum=0.00;QD=29.65;ReadPosRankSum=1.27;SOR=0.346	GT:AD:DP:GQ:PL	1:0,170:170:99:6854,0	1:0,198:198:99:8098,0	1:0,136:136:99:5554,0	1:0,141:141:99:5661,0	1:1,155:156:99:6327,0
ref	147463	.	C	A	4885.61	Q5000	AC=1;AF=0.200;AN=5;BaseQRankSum=-7.720e-01;ClippingRankSum=0.00;DP=503;FS=0.000;MLEAC=1;MLEAF=0.200;MQ=60.00;MQRankSum=0.00;QD=35.03;ReadPosRankSum=-6.950e-01;SOR=0.278	GT:AD:DP:FT:GQ:PL	0:97,0:97:DP125;DP130:99:0,1800	0:104,0:104:DP125;DP130:99:0,1800	0:84,0:84:DP125;DP130:99:0,1800	1:1,128:129:DP130:99:4919,0	0:89,0:89:DP125;DP130:99:0,1800
ref	154578	.	A	G	32015.60	PASS	AC=5;AF=1.00;AN=5;DP=776;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;QD=25.82;SOR=0.902	GT:AD:DP:GQ:PL	1:0,152:152:99:6300,0	1:0,183:183:99:7608,0	1:0,137:137:99:5713,0	1:0,148:148:99:6040,0	1:0,156:156:99:6381,0
ref	203200	.	C	T	30880.60	PASS	AC=5;AF=1.00;AN=5;DP=752;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;QD=29.65;SOR=0.878	GT:AD:DP:FT:GQ:PL	1:0,161:161:PASS:99:6708,0	1:0,185:185:PASS:99:7602,0	1:0,136:136:PASS:99:5602,0	1:0,126:126:DP130:99:5080,0	1:0,144:144:PASS:99:5915,0
ref	231665	.	C	T	30074.60	PASS	AC=5;AF=1.00;AN=5;DP=735;FS=0.000;MLEAC=5;MLEAF=1.00;MQ=60.00;QD=33.23;SOR=0.938	GT:AD:DP:FT:GQ:PL	1:0,191:191:PASS:99:7867,0	1:0,159:159:PASS:99:6431,0	1:0,130:130:PASS:99:5299,0	1:0,129:129:DP130:99:5290,0	1:0,126:126:DP130:99:5214,0