The usage message for the primary sequence_handling script does not list the handlers by the correct number for each option. For example, NP_Quality_Assessment is listed as "17" but it is option 15 in script, so option 17 starts read mapping. Other handlers at the bottom of the list are also off by 2 values.
The usage message for the primary sequence_handling script does not list the handlers by the correct number for each option. For example, NP_Quality_Assessment is listed as "17" but it is option 15 in script, so option 17 starts read mapping. Other handlers at the bottom of the list are also off by 2 values.
Usage: sequence_handling
Where: is one of:
Recommended workflow:
1 | Quality_Assessment
2 | Adapter_Trimming
3 | Read_Mapping
4 | SAM_Processing
5 | Coverage_Mapping
6 | Haplotype_Caller
7 | Genomics_DB_Import
8 | Genotype_GVCFs
9 | Create_HC_Subset
10 | Variant_Recalibrator
11 | Variant_Filtering
12 | Variant_Analysis
Other handlers:
13 | GBS_Demultiplex (in progress)
14 | Quality_Trimming
15 | Realigner_Target_Creator
16 | Indel_Realigner
Nanopore workflow:
17 | NP_Quality_Assessment (in progress)
18 | NP_Adapter_Trimming (in progress)
19 | NP_Read_Mapping (in progress)
20 | NP_SAM_Processing (in progress)