mother

Input Quality Assessment


mother.1_phred33
mother.2_phred33

Statistics

Alignment stats
source: mother_result/mother_bwamem.sort.rmdup.readfiltered.bam
QC-passed reads71205444
QC-failed-reads0
Duplicates10487284
Mapped reads64073406(89.98%)
Paired reads71205444
Read135602722
Read235602722
Properly paired69591070(97.73%)
Reads with itself and mate mapped64049764
Singletons23642(0.03%)
Reads with mate mapped to a different chromosome711928
Reads with mate mapped to a different chr (mapQ at least 5)711928


Coverage stats
source: mother_result/mother_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 61.07%
Average coverage in target region 63.76
Percentage above 3065.64%
Percentage above 2073.85%
Percentage above 1082.78%
Percentage above 588.92%


Variant stats(filter applied)
source: mother_result/mother.extract_consensus.vcf
Samplemother
Number of variants31021
Number of SNPs29411
Number of indels1610
Transitions21778
Transversions7642
Ti/Tv Ratio2.85
Total heterozygotes18461
Ref/Alt heterozygotes18423
Alt/Alt heterozygotes38
Homozygotes12560


Venn Diagram

Showing overlapping of up to 5 variant output

Coverage Plot

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