|[dnaapler](https://hub.docker.com/r/staphb/dnaapler)<br/>[](https://hub.docker.com/r/staphb/dnaapler)|<ul><li>[0.1.0](dnaapler/0.1.0/)</li></ul> <ul><li>[0.4.0](dnaapler/0.4.0/)</li><li>[0.5.0]...
abricate --nopath --db vibrio /data/GCA_018083565.2_PDT000793508.2_genomic.fna | tee /data/abricate_vibrio.tsv Using nucl database vibrio: 8 sequences - 2024-Apr-30 Processing: /data/GCA_018083565.2_PDT000793508.2_genomic.fna #FILE SEQUENCE START END STRAND GENE COVERAGE COVERAGE_MAP GAPS ...
Transcription is reading (DNA/RNA) and making a copy of that information in (DNA/RNA). During transcription, ___. (a) the entire DNA strand opens up for complete gene transcription (b) non-coding sequences are removed from the RNA transcript (c) tRNA bri...
{A,C,G,T}), from either of the two reverse-complementary strands of a DNA molecule, or in either sense of the same genomic strand (an example shown in Fig. 1). With the widely available second-generation sequencers, single reads are short, uniform-length, accurate (on the order of ...
that takes a single nucleotide input sequence (in FASTA format), finds the desired start gene using blastx against an amino acid sequence database, checks that the start codon of this gene is found, and if so, then reorients the chromosome to begin with this gene on the forward strand. ...