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error of -d must be specified.
Hi I'm running medaka consensus for a metagenome assembly from nanopore reads. but it giving the error of "-d must be specified". I have tried to run the command from the same folder where .fasta files was located but error is keep coming.
Pls suggest.
Usage/command: medaka_consensus -i /media/majorram/Analysis_Data/singhrn/meta_assembly/raw_data/*.fastq -d /media/majorram/Analysis_Data/singhrn/meta_assembly/assembly_all/medaka_polis/all_assembly.fasta -o /media/majorram/Analysis_Data/singhrn/meta_assembly/assembly_all/medaka_polis/meda_poli_assembly -t 2 -m r941_min_sup_g507
medaka 1.6.1
Assembly polishing via neural networks. Medaka is optimized to work with the Flye assembler.
medaka_consensus [-h] -i
-h show this help text.
-i fastx input basecalls (required).
-d fasta input assembly (required).
-o output folder (default: medaka).
-g don't fill gaps in consensus with draft sequence.
-m medaka model, (default: r941_min_hac_g507).
Choices: r103_fast_g507 r103_hac_g507 r103_min_high_g345 r103_min_high_g360 r103_prom_high_g360 r103_sup_g507 r1041_e82_400bps_fast_g615 r1041_e82_400bps_hac_g615 r1041_e82_400bps_sup_g615 r104_e81_fast_g5015 r104_e81_hac_g5015 r104_e81_sup_g5015 r104_e81_sup_g610 r10_min_high_g303 r10_min_high_g340 r941_e81_fast_g514 r941_e81_hac_g514 r941_e81_sup_g514 r941_min_fast_g303 r941_min_fast_g507 r941_min_hac_g507 r941_min_high_g303 r941_min_high_g330 r941_min_high_g340_rle r941_min_high_g344 r941_min_high_g351 r941_min_high_g360 r941_min_sup_g507 r941_prom_fast_g303 r941_prom_fast_g507 r941_prom_hac_g507 r941_prom_high_g303 r941_prom_high_g330 r941_prom_high_g344 r941_prom_high_g360 r941_prom_high_g4011 r941_prom_sup_g507 r941_sup_plant_g610
Alternatively a .tar.gz/.hdf file from 'medaka train'.
-f Force overwrite of outputs (default will reuse existing outputs).
-x Force recreation of alignment index.
-t number of threads with which to create features (default: 1).
-b batchsize, controls memory use (default: 100).
-d must be specified.
Thanks rgds Ram