Input data and parameters 

Input

Analysis date: Tue Oct 31 14:11:25 GMT 2023
BAM file: SRX7354400.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): 41,742,648 / 41,709,172
Number of aligned pairs (without duplicates): 41,684,098
Total number of alignments: 89,817,040
Number of secondary alignments: 6,365,220
Number of non-unique alignments: 10,447,660
Aligned to genes: 70,943,514
Ambiguous alignments: 291,173
No feature assigned: 7,613,445
Missing chromosome in annotation: 521,248
Not aligned: 1,352,324

Reads genomic origin

Exonic: 70,943,514 / 90.31%
Intronic: 4,472,544 / 5.69%
Intergenic: 3,140,901 / 4%
Intronic/intergenic overlapping exon: 3,352,922 / 4.27%

Transcript coverage profile

5' bias: 0.29
3' bias: 0.24
5'-3' bias: 2.03

Junction analysis

Reads at junctions: 24,405,704
ACCT 5.45%
TCCT 4.47%
AGGT 4.33%
ATCT 4.22%
GCCT 3.52%
AGGA 2.86%
CCCT 2.86%
AGCT 2.41%
AGGC 2.32%
TTCT 2.18%
TCCC 2.14%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis