yujiehu0823's Stars
phac-nml/ecoli_serotyping
In silico prediction of E. coli serotype
SBRG/precise-db
A high-fidelity E. coli RNA-seq compendium
vmingchen/PacBioAssembly
Assemble E. coli's genome from long reads with high error rate from PacBio
behrimg/MuriSam
Scripts to assemble and analyze genomes for E. coli populations and clones
superphy/kmer
Using machine learning to predict E. coli phenotypes
DerrickWood/kraken2
The second version of the Kraken taxonomic sequence classification system
phac-nml/sistr_cmd
SISTR (Salmonella In Silico Typing Resource) command-line tool
katholt/typhoid
klebgenomics/Kleborate
kblin/ncbi-genome-download
Scripts to download genomes from the NCBI FTP servers
ParBLiSS/FastANI
Fast Whole-Genome Similarity (ANI) Estimation
lskatz/mashtree
:deciduous_tree: Create a tree using Mash distances
marbl/parsnp
Parsnp was designed to align the core genome of hundreds to thousands of bacterial genomes within a few minutes to few hours. Input can be both draft assemblies and finished genomes, and output includes variant (SNP) calls, core genome phylogeny and multi-alignments. Parsnp leverages contextual information provided by multi-alignments surrounding SNP sites for filtration/cleaning, in addition to existing tools for recombination detection/filtration and phylogenetic reconstruction.
arpcard/rgi
Resistance Gene Identifier (RGI). Software to predict resistomes from protein or nucleotide data, including metagenomics data, based on homology and SNP models.
arpcard/amr_curation
A public repository for collective curation of antimicrobial resistance (AMR) genes and mutations. Submit, discuss, and resolve AMR curation issues.
lipingfangs/Bacteriatool
bacteriatool is a corpus of python script to deal with a lot of problem about bacteria genome analysis. you can use it to manage the data created by resfinder.py(https://bitbucket.org/genomicepidemiology/resfinder.git) to build a csv matrix about the presence of drug resistance genes in different individuals by Resfinder2csv.py. you can use it to manage the data created by toxicity database :VFDB by blast2.7(default output) to build a csv matrix about the presence of drug toxicity genes in different individuals by VFDB2csv.py. you can use it to extract the information like "organism","isolation_source","host","country","lat_lon","collection_date","sample_name" of GBK(GCA) file form NCBI and create a csv matrix of your information.
phac-nml/staramr
Scans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
typhoidgenomics/genotyphi
Assign genotypes to Salmonella Typhi genomes based on VCF files (mapped to Typhi CT18 reference genome)
jhawkey/IS_mapper
IS mapping software
katholt/NGSchallenge
Data for the outbreak investigation software challenge session at the ASM NGS 2015 conference
katholt/plotTree
ylxdzsw/mo-generator
有针对性地表达自己的崇敬之心
katholt/srst2
Short Read Sequence Typing for Bacterial Pathogens
OpenGene/MutScan
Detect and visualize target mutations by scanning FastQ files directly
OpenGene/fastp
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
rrwick/Bandage
a Bioinformatics Application for Navigating De novo Assembly Graphs Easily
rrwick/Unicycler
hybrid assembly pipeline for bacterial genomes
tseemann/prokka
:zap: :aquarius: Rapid prokaryotic genome annotation
tseemann/snippy
:scissors: :zap: Rapid haploid variant calling and core genome alignment
tseemann/abricate
:mag_right: :pill: Mass screening of contigs for antimicrobial and virulence genes