Input data and parameters 

Input

Analysis date: Fri Jul 18 00:44:31 GMT 2025
BAM file: DE-2.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): 83,069,646 / 83,046,675
Number of aligned pairs (without duplicates): 83,017,779
Total number of alignments: 181,107,831
Number of secondary alignments: 14,991,510
Number of non-unique alignments: 23,121,669
Aligned to genes: 82,091,802
Ambiguous alignments: 599,490
No feature assigned: 75,286,151
Missing chromosome in annotation: 8,719
Not aligned: 0

Reads genomic origin

Exonic: 82,091,802 / 52.16%
Intronic: 62,939,845 / 39.99%
Intergenic: 12,346,306 / 7.85%
Intronic/intergenic overlapping exon: 4,385,610 / 2.79%

Transcript coverage profile

5' bias: 0.55
3' bias: 0.34
5'-3' bias: 1.3

Junction analysis

Reads at junctions: 46,959,895
ACCT 5.61%
AGGT 4.94%
TCCT 3.53%
AGGA 3.5%
ATCT 3.09%
AGCT 3.04%
GCCT 2.7%
AGGC 2.64%
CCCT 2.48%
AGAT 2.29%
AGGG 2.26%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis