split_libraries_fastq.py error with golay barcodes (mock-5 & -7) about mockrobiota HOT 8 CLOSED

mock-5$ split_libraries_fastq.py -i mock-forward-read.fastq.gz -o split_libraries -m sample-metadata.tsv -b mock-index-read.corrected.fastq.gz --rev_comp_mapping_barcodes
Traceback (most recent call last):
  File "/usr/local/bin/split_libraries_fastq.py", line 365, in <module>
    main()
  File "/usr/local/bin/split_libraries_fastq.py", line 344, in main
    for fasta_header, sequence, quality, seq_id in seq_generator:
  File "/usr/local/lib/python2.7/dist-packages/qiime/split_libraries_fastq.py", line 322, in process_fastq_single_end_read_file
    raise FastqParseError("Headers of barcode and read do not match. Can't continue. "
qiime.split_libraries_fastq.FastqParseError: Headers of barcode and read do not match. Can't continue. Confirm that the barcode fastq and read fastq that you are passing match one another.

mock-7$ split_libraries_fastq.py -i mock-forward-read.fastq -o split_libraries -m sample-metadata.edit.tsv -b mock-index-read.fastq --rev_comp_mapping_barcodes
Traceback (most recent call last):
  File "/usr/local/bin/split_libraries_fastq.py", line 365, in <module>
    main()
  File "/usr/local/bin/split_libraries_fastq.py", line 344, in main
    for fasta_header, sequence, quality, seq_id in seq_generator:
  File "/usr/local/lib/python2.7/dist-packages/qiime/split_libraries_fastq.py", line 317, in process_fastq_single_end_read_file
    parse_fastq(fastq_read_f, strict=False, phred_offset=phred_offset)):
  File "/usr/local/lib/python2.7/dist-packages/skbio/parse/sequences/fastq.py", line 174, in parse_fastq
    seqid)
skbio.parse.sequences._exception.FastqParseError: Failed qual conversion for seq id: ILLUMINA_0275:2:1101:1357:1952#ATAGGCGATCNN. This may be because you passed an incorrect value for phred_offset.