son
Input Quality Assessment
son.1_phred33son.2_phred33
Statistics
Alignment stats
source: son_result/son_bwamem.sort.rmdup.readfiltered.bam |
QC-passed reads | 138779950 |
QC-failed-reads | 0 |
Duplicates | 12571793 |
Mapped reads | 124428082(89.66%) |
Paired reads | 138779950 |
Read1 | 69389975 |
Read2 | 69389975 |
Properly paired | 135643864(97.74%) |
Reads with itself and mate mapped | 124356940 |
Singletons | 71142(0.05%) |
Reads with mate mapped to a different chromosome | 839981 |
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 30 | 83.35% |
Percentage above 20 | 88.11% |
Percentage above 10 | 92.85% |
Percentage above 5 | 95.17% |
Variant stats(filter applied)
source: son_result/son.extract_consensus.vcf |
Sample | son |
Number of variants | 31897 |
Number of SNPs | 30157 |
Number of indels | 1740 |
Transitions | 22306 |
Transversions | 7863 |
Ti/Tv Ratio | 2.84 |
Total heterozygotes | 19658 |
Ref/Alt heterozygotes | 19611 |
Alt/Alt heterozygotes | 47 |
Homozygotes | 12239 |
Venn Diagram
Showing overlapping of up to 5 variant output
Coverage Plot