Input data and parameters 

Input

Analysis date: Fri Jul 18 01:50:08 GMT 2025
BAM file: DE-4.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): 93,948,658 / 93,926,934
Number of aligned pairs (without duplicates): 93,895,752
Total number of alignments: 208,586,248
Number of secondary alignments: 20,710,656
Number of non-unique alignments: 30,022,681
Aligned to genes: 90,568,015
Ambiguous alignments: 656,686
No feature assigned: 87,330,852
Missing chromosome in annotation: 8,014
Not aligned: 0

Reads genomic origin

Exonic: 90,568,015 / 50.91%
Intronic: 72,364,513 / 40.68%
Intergenic: 14,966,339 / 8.41%
Intronic/intergenic overlapping exon: 4,799,963 / 2.7%

Transcript coverage profile

5' bias: 0.59
3' bias: 0.37
5'-3' bias: 1.37

Junction analysis

Reads at junctions: 52,511,629
AGGT 8.18%
ACCT 5.22%
TCCT 3.37%
AGGA 3.36%
ATCT 3.17%
AGCT 2.98%
AGGC 2.67%
GCCT 2.62%
CCCT 2.34%
AGAT 2.16%
AGGG 2.1%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis