Input data and parameters 

Input

Analysis date: Fri Jul 18 00:43:06 GMT 2025
BAM file: DE-3.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): 80,822,391 / 80,796,797
Number of aligned pairs (without duplicates): 80,767,510
Total number of alignments: 179,036,830
Number of secondary alignments: 17,417,642
Number of non-unique alignments: 25,432,890
Aligned to genes: 78,217,196
Ambiguous alignments: 579,030
No feature assigned: 74,799,522
Missing chromosome in annotation: 8,192
Not aligned: 0

Reads genomic origin

Exonic: 78,217,196 / 51.12%
Intronic: 61,570,472 / 40.24%
Intergenic: 13,229,050 / 8.65%
Intronic/intergenic overlapping exon: 4,235,563 / 2.77%

Transcript coverage profile

5' bias: 0.58
3' bias: 0.36
5'-3' bias: 1.31

Junction analysis

Reads at junctions: 45,530,061
AGGT 8.09%
ACCT 5.28%
AGGA 3.38%
TCCT 3.36%
ATCT 3.07%
AGCT 2.94%
GCCT 2.68%
AGGC 2.62%
CCCT 2.33%
AGAT 2.2%
AGGG 2.16%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis