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Output Data
alexandriai168 edited this page Sep 11, 2023
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These files are found in the muri_metabarcoding/final_output/csv_output
directory. All files will have the {RUN NAME} and {PRIMER} as a prefix in the file name. For example: MURI306_DL_hash_key.fasta
hash key csv | CSV file with 2 columns: DNA sequence and Hash that matches with the sequence |
hash key fasta | same information as CSV file but in FASTA format (can be an input for BLAST) |
ASV table | CSV with sample name, primer, hash, # of reads per sequence |
taxonomy output | CSV with hash, sequence, and taxonomy assignments |
These files are found in the muri_metabarcoding/final_output/rdata_output
directory. All files will have the {RUN NAME} as a prefix and {PRIMER} at the end in the file name. For example: MURI306_output_DL.Rdata
When you load this Rdata file into R, it creates the following objects in your R global environment:
cleaned.seqtab.nochim | sample name on rows and DNA sequence in columns. Frequency of each sequence per sample |
freq.nochim | proportion of reads that were chimeras |
track | tracking of how many reads were filtered out during each step of the script |
joined_old_new_taxa | taxonomy output with hash, sequence, and taxonomy assignments |
where_trim_all_Fs | where quality trimming algorithm trimmed for forward sequences |
where_trim_all_Rs | where quality trimming algorithm trimmed for reverse sequences |
These files are found in the muri_metabarcoding/final_output/logs
directory.
tax_bootstrap.csv | taxonomy assignments (same as the taxonomy output) with the bootstrap confidence scores |
cutadapt_reports | directory of reports from each sample from primer trimming using cutadapt |
filtered_out_asv.csv | asv's filtered out by length after merging are saved in this csv file |