A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.
Report generated on 2026-08-24, 15:14 based on data in:
/projectnb/wax-dk/max/G216_MM9/SAMPLES/projectnb/wax-dk/max/G216_MM9/Scripts/03_FASTQC/projectnb/wax-dk/max/G216_MM9/Scripts/06_CollectMetrics
General Statistics
Showing 37/37 rows and 3/4 columns.| Sample Name | M Reads Mapped | % Assigned | M Assigned |
|---|---|---|---|
| G216_M01_sorted | 93.7% | 8.3 | |
| G216_M02_sorted | 95.7% | 7.2 | |
| G216_M03_sorted | 95.1% | 11.6 | |
| G216_M04_sorted | 95.3% | 5.8 | |
| G216_M05_sorted | 95.3% | 7.9 | |
| G216_M06_sorted | 95.9% | 8.9 | |
| G216_M07_sorted | 94.4% | 9.3 | |
| G216_M08_sorted | 95.1% | 9.4 | |
| G216_M09_sorted | 94.5% | 13.9 | |
| G216_M10_sorted | 96.0% | 7.3 | |
| G216_M11_sorted | 96.0% | 7.2 | |
| G216_M12_sorted | 94.8% | 9.6 | |
| G216_M37_sorted | 94.4% | 9.6 | |
| G216_M38_sorted | 94.5% | 9.7 | |
| G216_M39_sorted | 94.3% | 7.8 | |
| G216_M40_sorted | 94.7% | 8.6 | |
| G216_M41_sorted | 94.8% | 8.8 | |
| G216_M42_sorted | 96.1% | 7.7 | |
| G216_M43_sorted | 95.1% | 11.2 | |
| G216_M44_sorted | 94.8% | 10.5 | |
| G216_M45_sorted | 94.2% | 8.6 | |
| G216_M46_sorted | 96.1% | 6.1 | |
| G216_M47_sorted | 96.2% | 5.9 | |
| G216_M48_sorted | 94.7% | 7.2 | |
| G216_M61_sorted | 94.2% | 7.6 | |
| G216_M62_sorted | 94.4% | 5.8 | |
| G216_M63_sorted | 95.5% | 9.5 | |
| G216_M64_sorted | 95.1% | 6.6 | |
| G216_M65_sorted | 95.0% | 11.1 | |
| G216_M66_sorted | 94.5% | 9.4 | |
| G216_M67_sorted | 94.8% | 8.2 | |
| G216_M68_sorted | 94.4% | 11.4 | |
| G216_M69_sorted | 94.6% | 8.9 | |
| G216_M70_sorted | 95.2% | 8.0 | |
| G216_M71_sorted | 95.6% | 17.9 | |
| G216_M72_sorted | 92.9% | 8.4 | |
| statistics_for_primary_unique_reads | 16.7 |
RSeQC
RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput RNA-seq data.
Infer experiment
Infer experiment counts the percentage of reads and read pairs that match the strandedness of overlapping transcripts. It can be used to infer whether RNA-seq library preps are stranded (sense or antisense).
featureCounts
Subread featureCounts is a highly efficient general-purpose read summarization program that counts mapped reads for genomic features such as genes, exons, promoter, gene bodies, genomic bins and chromosomal locations.
Samtools
Samtools is a suite of programs for interacting with high-throughput sequencing data.
Samtools Flagstat
This module parses the output from samtools flagstat. All numbers in millions.