RECENT POSTS
- Introduction to FreeBSD Security Best Practices
- Working with Package Management in FreeBSD
- Understanding FreeBSD Security Advisories and Updates
- Troubleshooting Common System Administration Issues in FreeBSD
- Tips for Hardening FreeBSD to achieve System Protection
- Setting Up DHCP Server in FreeBSD
- Secure User and Group Management in FreeBSD Systems
- Secure Remote Access with SSH in FreeBSD
- Optimizing System Performance in FreeBSD
- Network Packet Capture with tcpdump in FreeBSD
- All posts ...
Do you have GDPR compliance issues ?
Check out Legiscope a GDPR compliance software, that will save you weeks of work, automating your documentation, the training of your teams and all processes you need to keep your organisation compliant with privacy regulations
Py-pyrodigal
Jul 20, 2023
Python binding for Prodigal, an ORF finder for genomes and metagenomes
Pyrodigal is a Python module that provides bindings to Prodigal using Cython.
Features The library now features everything from the original Prodigal CLI
- run mode selection Choose between single mode, using a training sequence to count nucleotide hexamers, or metagenomic mode, using pre-trained data from different organisms prodigal -p.
- region masking Prevent genes from being predicted across regions containing unknown nucleotides prodigal -m.
- closed ends Genes will be identified as running over edges if they are larger than a certain size, but this can be disabled prodigal -c.
- training configuration During the training process, a custom translation table can be given prodigal -g, and the Shine-Dalgarno motif search can be forcefully bypassed prodigal -n
- output files Output files can be written in a format mostly compatible with the Prodigal binary, including the protein translations in FASTA format prodigal -a, the gene sequences in FASTA format prodigal -d, or the potential gene scores in tabular format prodigal -s.
- Older
- Newer
Checkout these related ports:
- Wise - Intelligent algorithms for DNA searches
- Wfa2-lib - Exact gap-affine algorithm using homology to accelerate alignment
- Vt - Discovers short variants from Next Generation Sequencing data
- Vsearch - Versatile open-source tool for metagenomics
- Viennarna - Alignment tools for the structural analysis of RNA
- Velvet - Sequence assembler for very short reads
- Vcftools - Tools for working with VCF genomics files
- Vcflib - C++ library and CLI tools for parsing and manipulating VCF files
- Vcf2hap - Generate .hap file from VCF for haplohseq
- Vcf-split - Split a multi-sample VCF into single-sample VCFs
- Unikmer - Toolkit for nucleic acid k-mer analysis, set operations on k-mers
- Unanimity - Pacific Biosciences consensus library and applications
- Ugene - Integrated bioinformatics toolkit
- Ucsc-userapps - Command line tools from the UCSC Genome Browser project
- Trimmomatic - Flexible read trimming tool for Illumina NGS data