Genomic Contig Summary
segul contig summary calculates summary statistics for assembled contigs in FASTA format. For raw reads, see Genomic Read Summary.
Input formats
Section titled “Input formats”- Gunzip Compressed FASTA (.fa.gz/.fasta.gz)
- Standard FASTA (.fa/.fasta)
segul contig summary -i contigs.faor using directory input:
segul contig summary -d /contig_read_dirUse --output (or -o) to set the output directory and --prefix to set the prefix of the output files:
segul contig summary -d /contig_read_dir -o contig_output --prefix my_contig_summaryStatistics
Section titled “Statistics”Available statistics for contiguous sequences:
- Contig count
- Base count
- Nucleotide
- GC content
- AT content
- Minimum contig length
- Maximum contig length
- Mean contig length
- Median contig length
- N50
- N75
- N90
- Contig 750 bp
- Contig 1000 bp
- Contig 1500 bp
- Cumulative length
- A, C, G, T, N counts
All options
Section titled “All options”| Option | Description |
|---|---|
-d, --dir |
Directory with contig files |
-i, --input |
Contig files. Allows wildcards |
-f, --input-format |
Input format: auto (default), fasta, or gzip |
-o, --output |
Output directory. Default: Contig-Summary |
--prefix |
Prefix of the output files |
--force |
Overwrite an existing output directory |
--log |
Log file path. Default: segul.log |
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