Number of sequenced reads aligned to reference genome | 72 070 |
Number of sequenced nucleotides | 15 100 000 |
Median of reads per patient (IQR) | 2540 (2488) |
Mean number of haplotypes per patient after ShoRAH | 30.6 |
• Responders | 38.4 |
• Non-responders | 23.4 |
Most abundant haplotype | 57.09% |
Least abundant haplotype | 0.1% |