mother
Input Quality Assessment
mother.1_phred33mother.2_phred33
Statistics
Alignment stats
source: mother_result/mother_bwamem.sort.rmdup.readfiltered.bam |
QC-passed reads | 71205444 |
QC-failed-reads | 0 |
Duplicates | 10487284 |
Mapped reads | 64073406(89.98%) |
Paired reads | 71205444 |
Read1 | 35602722 |
Read2 | 35602722 |
Properly paired | 69591070(97.73%) |
Reads with itself and mate mapped | 64049764 |
Singletons | 23642(0.03%) |
Reads with mate mapped to a different chromosome | 711928 |
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 30 | 65.64% |
Percentage above 20 | 73.85% |
Percentage above 10 | 82.78% |
Percentage above 5 | 88.92% |
Variant stats(filter applied)
source: mother_result/mother.extract_consensus.vcf |
Sample | mother |
Number of variants | 31021 |
Number of SNPs | 29411 |
Number of indels | 1610 |
Transitions | 21778 |
Transversions | 7642 |
Ti/Tv Ratio | 2.85 |
Total heterozygotes | 18461 |
Ref/Alt heterozygotes | 18423 |
Alt/Alt heterozygotes | 38 |
Homozygotes | 12560 |
Venn Diagram
Showing overlapping of up to 5 variant output
Coverage Plot