son

Input Quality Assessment


son.1_phred33
son.2_phred33

Statistics

Alignment stats
source: son_result/son_bwamem.sort.rmdup.readfiltered.bam
QC-passed reads138779950
QC-failed-reads0
Duplicates12571793
Mapped reads124428082(89.66%)
Paired reads138779950
Read169389975
Read269389975
Properly paired135643864(97.74%)
Reads with itself and mate mapped124356940
Singletons71142(0.05%)
Reads with mate mapped to a different chromosome839981
Reads with mate mapped to a different chr (mapQ at least 5)839981


Coverage stats
source: son_result/son_bwamem.sort.rmdup.readfiltered.bam
total length (defined by /home/yunfeiguo/projects/seqmule_parallel/bin/secondary/../../misc/hg19_exome.bed) 46.21Mb
Fraction of reads mapped to target region 52.49%
Average coverage in target region 113.44
Percentage above 3083.35%
Percentage above 2088.11%
Percentage above 1092.85%
Percentage above 595.17%


Variant stats(filter applied)
source: son_result/son.extract_consensus.vcf
Sampleson
Number of variants31897
Number of SNPs30157
Number of indels1740
Transitions22306
Transversions7863
Ti/Tv Ratio2.84
Total heterozygotes19658
Ref/Alt heterozygotes19611
Alt/Alt heterozygotes47
Homozygotes12239


Venn Diagram

Showing overlapping of up to 5 variant output

Coverage Plot

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