Input data and parameters 

Input

Analysis date: Mon Oct 30 11:14:11 GMT 2023
BAM file: SRX7354168.markdup.sorted.bam
Counting algorithm: uniquely-mapped-reads
GTF file: gencode.v44.annotation_genes_collapsed_only_patched_ERCC92.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): 39,647,906 / 39,626,495
Number of aligned pairs (without duplicates): 39,623,385
Total number of alignments: 84,451,008
Number of secondary alignments: 5,176,607
Number of non-unique alignments: 8,437,724
Aligned to genes: 67,877,665
Ambiguous alignments: 231,390
No feature assigned: 7,478,344
Missing chromosome in annotation: 425,885
Not aligned: 2,399,353

Reads genomic origin

Exonic: 67,877,665 / 90.08%
Intronic: 4,885,422 / 6.48%
Intergenic: 2,592,922 / 3.44%
Intronic/intergenic overlapping exon: 2,346,326 / 3.11%

Transcript coverage profile

5' bias: 0.29
3' bias: 0.2
5'-3' bias: 1.77

Junction analysis

Reads at junctions: 22,286,107
ACCT 5.35%
AGGT 4.49%
ATCT 3.66%
GCCT 3.46%
TCCT 3.42%
AGGA 3.37%
AGCT 2.72%
AGGC 2.34%
CCCT 2.33%
TTCT 2.15%
AGAT 2.07%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis