Input data and parameters 

Input

Analysis date: Fri Jul 18 01:40:56 GMT 2025
BAM file: DE-6.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): 89,064,449 / 89,032,378
Number of aligned pairs (without duplicates): 89,001,182
Total number of alignments: 203,249,203
Number of secondary alignments: 25,152,376
Number of non-unique alignments: 36,338,769
Aligned to genes: 85,197,788
Ambiguous alignments: 600,203
No feature assigned: 81,101,841
Missing chromosome in annotation: 10,602
Not aligned: 0

Reads genomic origin

Exonic: 85,197,788 / 51.23%
Intronic: 65,873,809 / 39.61%
Intergenic: 15,228,032 / 9.16%
Intronic/intergenic overlapping exon: 4,426,978 / 2.66%

Transcript coverage profile

5' bias: 0.48
3' bias: 0.29
5'-3' bias: 1.43

Junction analysis

Reads at junctions: 50,118,718
AGGT 8.44%
ACCT 5.11%
AGGA 3.52%
TCCT 3.46%
AGGC 3.24%
AGCT 3%
ATCT 2.93%
GCCT 2.51%
CCCT 2.29%
AGAT 2.25%
AGGG 2.23%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis