rega-cev / virulignLinks
VIRULIGN: fast codon-correct alignment and annotation of viral genomes
☆35Updated 4 years ago
Alternatives and similar repositories for virulign
Users that are interested in virulign are comparing it to the libraries listed below
Sorting:
- Reference-guided multiple sequence alignment of viral genomes☆70Updated 3 months ago
- A nextflow pipeline for decontamination of short reads, long reads and contigs☆53Updated 2 months ago
- OPAL: Open-community Profiling Assessment tooL☆29Updated 8 months ago
- Find Unique genomic Regions☆30Updated this week
- A versatile toolkit for k-mers with taxonomic information☆79Updated 3 weeks ago
- Influenza genome analysis Nextflow workflow☆22Updated this week
- Converts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI☆29Updated 6 years ago
- SHOOT.bio - the phylogenetic search engine☆25Updated 2 years ago
- ☆41Updated last year
- Design degenerated primers on highly variable alignments for full genome sequencing or qPCR. Specifically developed for viruses.☆41Updated last month
- 🍊 💫 Trim, circularise and orient long read bacterial genome assemblies☆25Updated 6 years ago
- Protein Alignment and Detection Interface☆60Updated last year
- CAMITAX: Taxon labels for microbial genomes☆30Updated last year
- Tutorial for bacterial GWAS pipline and bugwas, created for Bodega Bay 2016 NGS workshop☆18Updated 9 years ago
- Utility program for extracting sequences from a fasta/fastq file☆35Updated 8 months ago
- Detection of incorrectly labeled sequences across kingdoms☆85Updated 2 years ago
- More realistic simulator for genomic DNA sequences from Illumina machines that achieves a similar k-mer spectrum as the original☆51Updated 3 years ago
- MutTui pipeline to reconstruct mutational spectra for bacterial and viral datasets☆29Updated last year
- PoSeiDon: positive selection detection and recombination analysis pipeline☆38Updated this week
- Convert genbank files to a swath of other formats☆18Updated last year
- Quantifying the significance of genetic variation using probabilistic profile-based methods.☆19Updated 4 years ago
- Get microbial sequence data easier and faster☆28Updated 5 years ago
- Assembler for raw de novo genome assembly of long uncorrected reads.☆36Updated 5 years ago
- Given a reference, PhaME extracts SNPs from complete genomes, draft genomes and/or reads. Uses SNP multiple sequence alignment to constr…☆33Updated last year
- PARTIE is a program to partition sequence read archive (SRA) metagenomics data into amplicon and shotgun data sets. The user-supplied ann…☆25Updated 2 years ago
- ☆26Updated 2 years ago
- Visualization of the pan-genome output by panX☆64Updated 3 months ago
- frame-shift correction for long-read (meta)genomics☆33Updated last year
- A pipeline for high-quality bacterial genome construction using ONT sequencing☆39Updated 2 years ago
- Output FASTQ summary statistics in JSON format☆29Updated 2 years ago