Input data and parameters 

Input

Analysis date: Fri Mar 25 19:24:46 GMT 2022
BAM file: gonad.markdup.sorted.bam
Counting algorithm: uniquely-mapped-reads
GTF file: Panopea-generosa-v1.0.a4_biotype-trna_strand_converted-no_RNAmmer.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): 41,072,342 / 41,059,764
Number of aligned pairs (without duplicates): 41,017,159
Total number of alignments: 88,696,621
Number of secondary alignments: 6,564,515
Number of non-unique alignments: 11,027,828
Aligned to genes: 20,060,305
Ambiguous alignments: 100
No feature assigned: 57,608,388
Not aligned: 0

Reads genomic origin

Exonic: 20,060,305 / 25.83%
Intronic: 16,547,866 / 21.31%
Intergenic: 41,060,522 / 52.87%
Intronic/intergenic overlapping exon: 5,329,654 / 6.86%

Transcript coverage profile

5' bias: 0.56
3' bias: 0.53
5'-3' bias: 1.06

Junction analysis

Reads at junctions: 28,937,910
AGGT 6.63%
ACCT 4.92%
AGAT 4.05%
AGTT 3.22%
AGGA 2.79%
ATCT 2.74%
TCCT 2.69%
AGGC 2.55%
AGCT 2.2%
AGAG 2.12%
AGAA 2.11%

Reads Genomic Origin 

Coverage Profile Along Genes (Total) 

Coverage Profile Along Genes (Low) 

Coverage Profile Along Genes (High) 

Coverage Histogram (0-50X) 

Junction Analysis