Input data and parameters 

Input

Analysis date: Fri Jul 18 00:27:31 GMT 2025
BAM file: HB.markdup.sorted.bam
Counting algorithm: uniquely-mapped-reads
GTF file: genes.filtered.gtf
Number of bases for 5'-3' bias computation: 100
Number of transcripts for 5'-3' bias computation: 1,000
Paired-end sequencing: yes
Protocol: strand-specific-reverse
Sorting performed: yes

Summary 

Reads alignment

Number of mapped reads (left/right): 75,371,867 / 75,344,465
Number of aligned pairs (without duplicates): 75,319,060
Total number of alignments: 171,984,511
Number of secondary alignments: 21,268,179
Number of non-unique alignments: 30,836,676
Aligned to genes: 74,866,738
Ambiguous alignments: 528,243
No feature assigned: 65,742,906
Missing chromosome in annotation: 9,948
Not aligned: 0

Reads genomic origin

Exonic: 74,866,738 / 53.24%
Intronic: 52,762,156 / 37.52%
Intergenic: 12,980,750 / 9.23%
Intronic/intergenic overlapping exon: 3,915,719 / 2.78%

Transcript coverage profile

5' bias: 0.56
3' bias: 0.37
5'-3' bias: 1.31

Junction analysis

Reads at junctions: 41,983,162
AGGT 10.07%
ACCT 4.97%
AGGA 3.38%
TCCT 3.29%
AGCT 2.94%
ATCT 2.85%
GCCT 2.54%
AGGC 2.51%
CCCT 2.26%
AGGG 2.22%
AGAT 2.19%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis