Open michaelforthman opened 3 years ago
Also, I have ">" at the beginning of each fasta header. For some reason github keeps interpreting it as a quote and removes it.
Part of this is an issue with moving to python3. That said, I would use another tool to split these reads - I'm likely to just remove this code in an updated version. I'd look into seqtk (should come w/ phyluce), bbmap, or you could use something like galaxy (https://galaxyproject.org/support/ncbi-sra-fastq/#interleaved-forward-and-reverse-reads).
For example, in seqtk, you would do something like:
seqtk seq interleaved.fq -1 > read_1.fq
seqtk seq interleaved.fq -2 > read_2.fq
Hi Brant,
I'm getting some errors when attempting to unmix fasta reads, with error messages varying between different phyluce versions.
1.7.1 and 1.7.0 error:
Earlier versions error:
Below is an example of how my fasta files are formatted and my job code: `
phyluce_utilities_unmix_fasta_reads --mixed-reads /blue/cwmiller/mforthman/coreoidea_phylogenomics_part2/genomic_transcriptomic_reads_for_mapping/quorum_output/Arocatus_melanocephalus_SRR2051471_mapped_reads_corrected.fasta --out-r1 /blue/cwmiller/mforthman/coreoidea_phylogenomics_part2/genomic_transcriptomic_reads_for_mapping/quorum_output/Arocatus_melanocephalus_SRR2051471_mapped_corrected_R1.fasta --out-r2 /blue/cwmiller/mforthman/coreoidea_phylogenomics_part2/genomic_transcriptomic_reads_for_mapping/quorum_output/Arocatus_melanocephalus_SRR2051471_mapped_corrected_R2.fasta --out-r-singleton /blue/cwmiller/mforthman/coreoidea_phylogenomics_part2/genomic_transcriptomic_reads_for_mapping/quorum_output/Arocatus_melanocephalus_SRR2051471_mapped_corrected_singles.fasta
Is there an issue with my fasta file or code that I'm not seeing?
Thanks, Michael