drhchen's starred repositories

adegenet

adegenet: a R package for the multivariate analysis of genetic markers

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RiDiCulousFilter

Filter sequences based on a variety of conditions

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KMC

Fast and frugal disk based k-mer counter

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kounta

🧮 🔢 Generate multi-sample k-mer count matrix from WGS

Language:PerlLicense:GPL-3.0Stargazers:10Issues:0Issues:0

kmersGWAS

A library for running k-mers based GWAS

Language:C++License:GPL-3.0Stargazers:99Issues:0Issues:0

binary_tree

To convert gene-presence-absence matrix into multi fasta alignment

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orthocounts2bin

A script to get from Orthogroups.GeneCount.tsv to a gene presence/absence binary alignment.

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GenAPI

Gene Absence Presence Identification tool.

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matrix_converter

Small matrix converter tool for my design project

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treeWAS

treeWAS: A Phylogenetic Tree-Based Tool for Genome-Wide Association Studies in Microbes

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ClonalFrameML

ClonalFrameML: Efficient Inference of Recombination in Whole Bacterial Genomes

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dsk

k-mer counting software

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ISseeker

A tool to find Insertion Sequences by blasting their flanking sequences against a reference.

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gubbins

Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins

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mlst

:id: Scan contig files against PubMLST typing schemes

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LS-BSR

Large scale Blast Score Ratio (BSR) analysis

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plasmidtron

Assembling the cause of phenotypes and genotypes from NGS data

Language:PythonLicense:GPL-3.0Stargazers:29Issues:0Issues:0

seqfilter

Filter fasta/fastq(.gz) files by ID and/or sequence length

Language:CLicense:MITStargazers:14Issues:0Issues:0

SeqFilter

Versatile FASTA/FASTQ sequence file analysis and modification tool

Language:PerlLicense:MITStargazers:9Issues:0Issues:0

Roary

Rapid large-scale prokaryote pan genome analysis

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Scoary

Pan-genome wide association studies

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bac-genomics-scripts

Collection of scripts for bacterial genomics

Language:PerlLicense:GPL-3.0Stargazers:42Issues:0Issues:0

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.

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bacterial_GWAS_tutorial

Tutorial for bacterial GWAS pipline and bugwas, created for Bodega Bay 2016 NGS workshop

License:CC0-1.0Stargazers:19Issues:0Issues:0