Input data and parameters 

Input

Analysis date: Fri Jul 18 00:34:52 GMT 2025
BAM file: DE-5.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): 79,518,941 / 79,489,396
Number of aligned pairs (without duplicates): 79,463,438
Total number of alignments: 179,299,009
Number of secondary alignments: 20,290,672
Number of non-unique alignments: 29,685,007
Aligned to genes: 77,053,238
Ambiguous alignments: 548,580
No feature assigned: 72,003,855
Missing chromosome in annotation: 8,329
Not aligned: 0

Reads genomic origin

Exonic: 77,053,238 / 51.69%
Intronic: 58,629,076 / 39.33%
Intergenic: 13,374,779 / 8.97%
Intronic/intergenic overlapping exon: 3,979,962 / 2.67%

Transcript coverage profile

5' bias: 0.55
3' bias: 0.35
5'-3' bias: 1.35

Junction analysis

Reads at junctions: 45,044,548
AGGT 9.79%
ACCT 5.1%
TCCT 3.39%
AGGA 3.38%
ATCT 3.02%
AGCT 2.95%
GCCT 2.56%
AGGC 2.44%
CCCT 2.37%
AGAT 2.16%
AGGG 2.14%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis