Input data and parameters 

Input

Analysis date: Sun Oct 29 01:25:05 GMT 2023
BAM file: SRX7354125.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): 33,148,599 / 33,119,413
Number of aligned pairs (without duplicates): 33,115,303
Total number of alignments: 70,490,484
Number of secondary alignments: 4,222,472
Number of non-unique alignments: 6,977,656
Aligned to genes: 55,242,940
Ambiguous alignments: 223,402
No feature assigned: 7,745,307
Missing chromosome in annotation: 301,179
Not aligned: 7,596,120

Reads genomic origin

Exonic: 55,242,940 / 87.7%
Intronic: 5,167,106 / 8.2%
Intergenic: 2,578,201 / 4.09%
Intronic/intergenic overlapping exon: 2,155,217 / 3.42%

Transcript coverage profile

5' bias: 0.39
3' bias: 0.21
5'-3' bias: 2

Junction analysis

Reads at junctions: 19,262,918
ACCT 5.32%
AGGT 4.9%
ATCT 3.63%
AGGA 3.51%
TCCT 3.44%
GCCT 3.1%
AGCT 2.79%
CCCT 2.53%
AGGC 2.48%
AGAT 2.13%
TTCT 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