Input data and parameters 

Input

Analysis date: Fri Jul 18 00:35:28 GMT 2025
BAM file: DE-3C.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): 78,856,641 / 78,834,962
Number of aligned pairs (without duplicates): 78,811,152
Total number of alignments: 176,633,950
Number of secondary alignments: 18,942,347
Number of non-unique alignments: 27,805,748
Aligned to genes: 84,674,432
Ambiguous alignments: 633,267
No feature assigned: 63,513,059
Missing chromosome in annotation: 7,444
Not aligned: 0

Reads genomic origin

Exonic: 84,674,432 / 57.14%
Intronic: 50,221,592 / 33.89%
Intergenic: 13,291,467 / 8.97%
Intronic/intergenic overlapping exon: 4,285,356 / 2.89%

Transcript coverage profile

5' bias: 0.58
3' bias: 0.37
5'-3' bias: 1.3

Junction analysis

Reads at junctions: 49,959,947
AGGT 8.58%
ACCT 5.22%
AGGA 3.36%
TCCT 3.33%
ATCT 3.03%
AGCT 2.91%
GCCT 2.63%
AGGC 2.54%
CCCT 2.34%
AGAT 2.17%
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