Input data and parameters 

QualiMap command line

qualimap bamqc -bam SRR389222_sub1_trimmed_bismark_bt2.deduplicated.sorted.bam -nw 400 -hm 3

Alignment

Command line: "bismark SRR389222_sub1_trimmed.fq.gz --bowtie2 --bam --genome BismarkIndex"
Draw chromosome limits: no
Analyze overlapping paired-end reads: yes
Program: Bismark (v0.23.1)
Analysis date: Mon Sep 13 13:42:14 MSK 2021
Size of a homopolymer: 3
Skip duplicate alignments: no
Number of windows: 400
BAM file: SRR389222_sub1_trimmed_bismark_bt2.deduplicated.sorted.bam

Summary 

Globals

Reference size 48,502
Number of reads 310
Mapped reads 310 / 100%
Unmapped reads 0 / 0%
Mapped paired reads 0 / 0%
Secondary alignments 0
Read min/max/mean length 20 / 36 / 35.14
Overlapping read pairs 0 / 0%
Duplicated reads (estimated) 9 / 2.9%
Duplication rate 2.99%
Clipped reads 0 / 0%

ACGT Content

Number/percentage of A's 2,735 / 25.11%
Number/percentage of C's 110 / 1.01%
Number/percentage of T's 4,796 / 44.04%
Number/percentage of G's 3,250 / 29.84%
Number/percentage of N's 2 / 0.02%
GC Percentage 30.85%

Coverage

Mean 0.2246
Standard Deviation 2.7428

Mapping Quality

Mean Mapping Quality 0.4

Mismatches and indels

General error rate 25.69%
Mismatches 2,798

Chromosome stats

Name Length Mapped bases Mean coverage Standard deviation
chr 48502 10893 0.2246 2.7428

Coverage across reference 

Coverage Histogram 

Coverage Histogram (0-50X) 

Genome Fraction Coverage 

Duplication Rate Histogram 

Mapped Reads Nucleotide Content 

Mapped Reads GC-content Distribution 

Mapping Quality Across Reference 

Mapping Quality Histogram