A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.
Report
generated on 2023-06-01, 12:01
based on data in:
/mnt/lustre/users/apostmasmidt/Deladenus/RNASeqMacrogen2023/hisat/summary
General Statistics
Showing 21/21 rows.Sample Name | % Aligned |
---|---|
C587R1.hisat | 80.3% |
C587R2.hisat | 75.1% |
C587R3.hisat | 76.7% |
C595R1.hisat | 72.3% |
C595R2.hisat | 75.9% |
C595R3.hisat | 70.4% |
C756R1.hisat | 74.8% |
C756R2.hisat | 83.0% |
C756R3.hisat | 77.2% |
C788R1.hisat | 77.6% |
C788R2.hisat | 81.6% |
C788R3.hisat | 80.2% |
P587R1.hisat | 79.6% |
P587R2.hisat | 74.8% |
P587R3.hisat | 80.2% |
P756R1.hisat | 82.7% |
P756R2.hisat | 85.1% |
P756R3.hisat | 78.6% |
P788R1.hisat | 78.1% |
P788R2.hisat | 80.7% |
P788R3.hisat | 78.7% |
HISAT2
HISAT2 is a fast and sensitive alignment program for mapping NGS reads (both DNA and RNA) against a reference genome or population of reference genomes.DOI: 10.1038/nmeth.3317; 10.1038/s41587-019-0201-4.
Please note that single mate alignment counts are halved to tally with pair counts properly.