view test-data/split_libraries/split_library_log @ 7:9d06d3380f1d draft default tip

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/qiime/ commit c845cb240f57663cf1e2240c5c506ea0b294872c"

Number raw input seqs	8

Length outside bounds of 200 and 1000	0
Num ambiguous bases exceeds limit of 6	0
Missing Qual Score	0
Mean qual score below minimum of 25	0
Max homopolymer run exceeds limit of 6	0
Num mismatches in primer exceeds limit of 0: 0

Sequence length details for all sequences passing quality filters:
Raw len min/max/avg	244.0/276.0/255.5
Wrote len min/max/avg	211.0/243.0/222.5

Barcodes corrected/not	0/0
Uncorrected barcodes will not be written to the output fasta file.
Corrected barcodes will be written with the appropriate barcode category.
Corrected but unassigned sequences will not be written unless --retain_unassigned_reads is enabled.

Total valid barcodes that are not in mapping file	0
Sequences associated with valid barcodes that are not in the mapping file will not be written.

Barcodes in mapping file
Num Samples	3
Sample ct min/max/mean: 2 / 4 / 2.67
Sample	Sequence Count	Barcode
PC.634	4	ACAGAGTCGGCT
PC.354	2	AGCACGAGCCTA
PC.481	2	ACCAGCGACTAG
PC.593	0	AGCAGCACTTGT
PC.636	0	ACGGTGAGTGTC
PC.635	0	ACCGCAGAGTCA
PC.356	0	ACAGACCACTCA
PC.607	0	AACTGTGCGTAC
PC.355	0	AACTCGTCGATG

Total number seqs written	8