There are 1 repository under contigs topic.
:mag_right: :pill: Mass screening of contigs for antimicrobial and virulence genes
Redundans is a pipeline that assists an assembly of heterozygous/polymorphic genomes.
An efficient index for the colored, compacted, de Bruijn graph
Wally: Visualization of aligned sequencing reads and contigs
Identification & characterization of bacterial plasmid-borne contigs from short-read draft assemblies.
✨🧬 Refined binning of metagenomic contigs using assembly graphs
Genome scaffolding based on HiC data in heterozygous and high ploidy genomes
Scalable long read self-correction and assembly polishing with multiple sequence alignment
🚦🧬 Binning Metagenomic Contigs via Composition, Coverage and Assembly Graphs
☯️🧬 Refined and Overlapped Binning of Metagenomic Contigs Using Assembly Graphs
Simulate metagenomic short reads from one or more populations.
Small and simple scripts useful for various bioinformatics purposes e.g. extract sequences from fasta files
This pipeline is intended to be a convenient way to work though large sets of metagenomic or metatranscriptiomic datasets while also retaining high analytical flexibility due to retained intermediate results that might be useful outside of the intended purpose.
Software to identify plasmid sequence data from metagenome using logistic regression and Minhash
DEPRECATED: Discover divergent virus sequences, prune flanking cellular sequences, make basic report
Toolkit for binning FASTA, FASTQ and FAST5 files according to taxonomic annotation
Genome assembly - From theory to practice (and back)
Take information about snps on short sequence reads and accurately place the snps in a reference genome
BSc Senior Project, Bioinformatics Django web platform for storage and analysis of Biological data. Still in use by the group CHROMEVOL from FIU
get chloroplast and mitochondrial genes from contigs of genome-skimming or transcriptome data
Sequencing of unculturable plant pathogens
Refining Domain Boundaries and Performing Large Scale Parsing
hierarchical clustering of DNA sequence using upcxx
A comprehensive workflow for de novo assembly of whole-genome shotgun sequencing data using Velvet, followed by BLAST searches to analyze assembled contigs.
Split a multifasta file into many fasta files containing a single sequence, or extract a list of sequences/contigs. Supports compressed input and output files.