Name: WooSP
Type: User
Company: GI en Especies Leñosas/RG on Woody Species,Dpto. de Sistemas y Recursos Naturales. ETSI Montes, Forestal y del Medio Natural. Universidad Politécnica de Madrid
Bio: This is the software page of the Woody Species Research Group -WooSP- (inheritor of the GGFHF).
Location: ETSI Montes, Forestal y del Medio Natural. Ciudad Universitaria s/n. 28040. Madrid. Spain
Blog: https://blogs.upm.es/woosp/
WooSP's Projects
Workflow Bash and R scripts used to analyze demultiplexed SE reads from a ddRADseq experiment in Quercus suber, Quercus ilex, and their hybrids.
Software package for in silico simulation and testing of double digest RADseq experiments.
Differential Expression analysis pipelines benchmarking workflow based on Gold Standard construction
gtimputation (Genotype Imputation) is an application designed to determine the genotypes of missing data in a VCF or tabular format file using a machine learning procedure based on self-organizing maps (SOMs)
R scripts to analyze the distortion of the mendelian segregation patterns in Q. ilex x suber hybrid progenies
Now NGScloud is deprecated. You must use NGScloud2 at https://github.com/GGFHF/NGScloud2/.
NGScloud2, a major version of NGScloud, provides a user-friendly front-end to operate the EC2 resources and to control bioinformatic analysis workflows of NGS experiments in a modular way. The application allows to optimize the cost-efficiency ratio of NGS experiments when appropriate computational facilities are not available.
NGShelper is a set of tools useful to performance some tasks related to NGS analysis.
Bioinformatic workflow to choose the optimal genotyping strategy using RADs (ddRADseq-GBS) from individual-replicates pilot studies
Files corresponding to RNA-seq performance tests of NGScloud.
SimHyb2 is a educational and research java-based software to simulate virtual individuals from mixed hybridizing populations
TOA (Taxonomy-oriented Annotation) establishes workflows geared towards plant species that automate the extraction of information from genomic databases and the annotation of sequences.