Input data and parameters 

Input

Analysis date: Fri Jul 18 01:39:15 GMT 2025
BAM file: DE-1.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): 87,309,921 / 87,286,398
Number of aligned pairs (without duplicates): 87,258,574
Total number of alignments: 196,872,006
Number of secondary alignments: 22,275,687
Number of non-unique alignments: 33,760,422
Aligned to genes: 94,622,666
Ambiguous alignments: 704,333
No feature assigned: 67,777,956
Missing chromosome in annotation: 6,629
Not aligned: 0

Reads genomic origin

Exonic: 94,622,666 / 58.26%
Intronic: 54,624,925 / 33.64%
Intergenic: 13,153,031 / 8.1%
Intronic/intergenic overlapping exon: 4,515,279 / 2.78%

Transcript coverage profile

5' bias: 0.56
3' bias: 0.38
5'-3' bias: 1.25

Junction analysis

Reads at junctions: 55,579,144
ACCT 5.77%
AGGT 4.93%
AGGA 3.62%
TCCT 3.43%
AGGC 3.04%
AGCT 3.04%
ATCT 2.96%
GCCT 2.65%
CCCT 2.43%
AGAT 2.3%
AGGG 2.28%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis