A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.
Report generated on 2026-08-19, 08:06 based on data in:
/projectnb/wax-dk/max/G260_G264_RNAseq/G262v2_RNAseq/SAMPLES/projectnb/wax-dk/max/G260_G264_RNAseq/G262v2_RNAseq/Scripts/03_FASTQC/projectnb/wax-dk/max/G260_G264_RNAseq/G262v2_RNAseq/Scripts/06_CollectMetrics
General Statistics
Showing 54/54 rows and 3/4 columns.| Sample Name | M Reads Mapped | % Assigned | M Assigned |
|---|---|---|---|
| G262_M01_sorted | 93.8% | 10.5 | |
| G262_M02_sorted | 93.4% | 13.7 | |
| G262_M03_sorted | 93.5% | 14.4 | |
| G262_M04_sorted | 94.7% | 10.2 | |
| G262_M05_sorted | 93.6% | 17.5 | |
| G262_M06_sorted | 93.3% | 17.8 | |
| G262_M07_sorted | 95.6% | 15.5 | |
| G262_M08_sorted | 93.1% | 17.0 | |
| G262_M09_sorted | 92.3% | 15.9 | |
| G262_M10_sorted | 90.6% | 11.2 | |
| G262_M11_sorted | 93.0% | 18.0 | |
| G262_M12_sorted | 93.2% | 18.8 | |
| G262_M13_sorted | 94.7% | 13.6 | |
| G262_M16_sorted | 91.9% | 15.7 | |
| G262_M17_sorted | 92.6% | 15.2 | |
| G262_M18_sorted | 88.6% | 15.1 | |
| G262_M19_sorted | 93.5% | 17.2 | |
| G262_M20_sorted | 88.9% | 16.2 | |
| G262_M21_sorted | 92.8% | 19.0 | |
| G262_M22_sorted | 94.0% | 18.3 | |
| G262_M23_sorted | 89.5% | 16.2 | |
| G262_M25_sorted | 92.9% | 13.2 | |
| G262_M26_sorted | 93.4% | 14.1 | |
| G262_M27_sorted | 90.1% | 21.2 | |
| G262_M29_sorted | 92.3% | 9.6 | |
| G262_M30_sorted | 91.3% | 19.0 | |
| G262_M31_sorted | 94.8% | 18.7 | |
| G262_M32_sorted | 95.0% | 18.1 | |
| G262_M33_sorted | 93.1% | 19.2 | |
| G262_M34_sorted | 94.8% | 16.7 | |
| G262_M35_sorted | 94.4% | 15.3 | |
| G262_M36_sorted | 93.3% | 16.3 | |
| G262_M37_sorted | 93.8% | 13.0 | |
| G262_M39_sorted | 92.5% | 18.5 | |
| G262_M40_sorted | 90.1% | 19.6 | |
| G262_M41_sorted | 91.6% | 17.6 | |
| G262_M42_sorted | 92.0% | 21.4 | |
| G262_M43_sorted | 90.9% | 17.7 | |
| G262_M44_sorted | 90.8% | 17.4 | |
| G262_M45_sorted | 91.1% | 20.0 | |
| G262_M46_sorted | 94.2% | 22.9 | |
| G262_M47_sorted | 94.8% | 19.3 | |
| G262_M48_sorted | 93.8% | 20.9 | |
| G262_M50_sorted | 92.0% | 11.9 | |
| G262_M51_sorted | 92.5% | 13.8 | |
| G262_M52_sorted | 92.3% | 17.2 | |
| G262_M53_sorted | 92.0% | 18.5 | |
| G262_M54_sorted | 91.4% | 20.8 | |
| G262_M55_sorted | 93.1% | 15.9 | |
| G262_M56_sorted | 94.0% | 14.0 | |
| G262_M57_sorted | 93.4% | 9.0 | |
| G262_M58_sorted | 92.0% | 19.8 | |
| G262_M59_sorted | 91.9% | 17.9 | |
| statistics_for_primary_unique_reads | 36.5 |
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.