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emmadebayos's Projects

multigwas icon multigwas

MultiGWAS: A tool for GWAS analysis on tetraploid organisms by integrating results of four GWAS software

multiqc icon multiqc

Aggregate results from bioinformatics analyses across many samples into a single report.

novograph icon novograph

NovoGraph: building whole genome graphs from long-read-based de novo assemblies

phyling_unified icon phyling_unified

Unified PHYling pipeline for species tree building from annotated genomes (see https://github.com/stajichlab/AAFTF and https://github.com/nextgenusfs/funannotate for assembly and annotation steps)

pilon icon pilon

Pilon is an automated genome assembly improvement and variant detection tool

qtl-seq icon qtl-seq

QTL-seq pipeline to identify causative mutations responsible for a phenotype

qtlseqr icon qtlseqr

QTLseqr is an R package for QTL mapping using NGS Bulk Segregant Analysis

rnaseq-nf icon rnaseq-nf

RNASeq-NF is an NGS analysis pipeline for RNA expression quantification.

rnaseqview icon rnaseqview

RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon

scripts icon scripts

Scripts for analysis used during the course

snp-sites icon snp-sites

Finds SNP sites from a multi-FASTA alignment file

ssake icon ssake

๐ŸถGenome assembly with short sequence reads

star_protocols_wes3x icon star_protocols_wes3x

Functional code templates for the Star Protocols paper describing consolidated WES variant calling with 3 callers

sweep icon sweep

Sliding Window Extraction of Explicit Polymorphisms

tassel-workshop icon tassel-workshop

This site contains sample files and instructions for the TASSEL workshop hosted by the UMN Plant Breeding Center.

utilities icon utilities

A bunch of scripts for bioinformatic purposes

vcf2msa.py icon vcf2msa.py

Package for writing multiple sequence alignments of pseudo-references from a VCF file with a reference genome

xftools icon xftools

Tools developed for use in Xiaoqi Feng's lab.

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