Input data and parameters 

Input

Analysis date: Sun Oct 29 02:15:27 GMT 2023
BAM file: SRX7354090.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): 35,951,248 / 35,923,173
Number of aligned pairs (without duplicates): 35,918,315
Total number of alignments: 77,329,337
Number of secondary alignments: 5,454,916
Number of non-unique alignments: 8,646,276
Aligned to genes: 59,400,127
Ambiguous alignments: 227,016
No feature assigned: 8,421,595
Missing chromosome in annotation: 634,323
Not aligned: 3,428,711

Reads genomic origin

Exonic: 59,400,127 / 87.58%
Intronic: 5,015,247 / 7.39%
Intergenic: 3,406,348 / 5.02%
Intronic/intergenic overlapping exon: 2,438,599 / 3.6%

Transcript coverage profile

5' bias: 0.31
3' bias: 0.28
5'-3' bias: 1.63

Junction analysis

Reads at junctions: 22,125,176
ACCT 5.4%
AGGT 4.35%
TCCT 4.09%
ATCT 3.92%
GCCT 3.7%
AGGA 3.03%
CCCT 2.8%
AGCT 2.51%
AGGC 2.39%
TTCT 2.2%
TCCC 1.93%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis