Description Usage Arguments Value
View source: R/nanoRaw_scripts.R
Genome coverage of nanopore run Takes in the 'sequencing_summary' file of albacore and the genome fasta as input and returns the genome coverage
1 | nano_seq_cov(inputfile, genome_fasta, quality = 0)
|
inputfile |
Filepath to sequencing_summary.txt output of albacore |
genome_fasta |
path to genome fasta |
quality |
Mean quality filter option for every read |
Genome coverage = Nr of bases sequenced/genome length
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