Workflows

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834 Workflows visible to you, out of a total of 910
annotation-helixer/main

This workflow allows you to annotate a genome with Helixer and evaluate the quality of the annotation using BUSCO and Genome Annotation statistics. GFFRead is also used to predict protein sequences derived from this annotation, and BUSCO and OMArk are used to assess proteome quality.

Type: Galaxy

Creator: Romane Libouban

Submitter: WorkflowHub Bot

Allele-specific expression-network clustering analysis for Huntington's Disease
No description specified

Type: Common Workflow Language

Creators: None

Submitter: Aishwarya Iyer

nf-core/pixelator

GitHub Actions CI Status GitHub Actions Linting StatusAWS CI[![Cite ...

Type: Nextflow

Creator: Pixelgen Technologies AB

Submitter: WorkflowHub Bot

mettannotator
Stable

Nextflow run with docker run with singularity

mettannotator

Type: Nextflow

Creators: Tatiana Gurbich, Martin Beracochea

Submitter: Martin Beracochea

A workflow to extract individual trees from 3D point cloud data obtained by airborne laser scanning

Point-based Individual Tree Delineation from 3D LiDAR Point Cloud Data.

This module implements a lightweight and easy-to-use Point-based method for individual tree delineation from 3D point cloud data using pure C/C++.

The source code files are included in folder [TreeSeparation], which consists of a project generated from Visual Studio 2015. The CLASS for tree separation is named "FoxTree" and can be found in the respect FoxTree.h and FoxTree.cpp files.

Inupt

The ...

Type: Unrecognized workflow type

Creators: None

Submitter: Jinhu Wang

nf-core/rangeland

GitHub Actions CI Status GitHub Actions Linting StatusAWS CI[![Cite ...

Type: Nextflow

Creators: None

Submitter: WorkflowHub Bot

Use case 9: Explore regulatory information associated with a regulatory element

The workflow starts with selecting EH38E2924876 as the search term. Genomic position of provided unique regulatory element identifier was retrieved from CFDE Linked Data Hub[1]. A list of variants in the region of the regulatory element was retrieved from CFDE Linked Data Hub[1]. Variant/variant set associated allele specific epigenomic signatures were retrieved from CFDE LDH[5] based on Roadmap and ENTEx data[6], [4]. GTEx eQTL and sQTL evidence for the given variant(s) were retrieved from CFDE ...

Type: Playbook Workflow Builder Workflow

Creator: Playbook Partnership NIH CFDE

Submitter: Daniel Clarke

DOI: 10.48546/workflowhub.workflow.1249.3

Use Case 3: Compounds to Reverse Disease Signatures

A file containing GEO Aging Signatures was first uploaded. The file containing GEO Aging Signatures was loaded as a gene signature. A file containing GTEx Aging Signatures was first uploaded. The file containing GTEx Aging Signatures was loaded as a gene signature. Significant genes were extracted from the GEO Aging Signatures. Significant genes were extracted from the GTEx Aging Signatures. Reversers and mimickers from over 1 million signatures were identified using SigCom LINCS[1]. Resolved ...

Type: Playbook Workflow Builder Workflow

Creator: Playbook Partnership NIH CFDE

Submitter: Daniel Clarke

DOI: 10.48546/workflowhub.workflow.1248.2

Use Case 13: Novel Cell Surface Targets for Individual Cancer Patients Analyzed with Common Fund Datasets

A file was first uploaded. The file was parsed as a gene count matrix. Significantly over-expressed genes when compared to tissue expression in GTEx[1] were identified. RNA-seq-like LINCS L1000 Signatures[3] which mimick or reverse the the expression of IMP3 were visualized. Drugs which down-regulate the expression of IMP3 were identified from the RNA-seq-like LINCS L1000 Chemical Perturbagens[3]. Genes which down-regulate the expression of IMP3 were identified from the RNA-seq-like LINCS L1000 ...

Type: Playbook Workflow Builder Workflow

Creator: Playbook Partnership NIH CFDE

Submitter: Daniel Clarke

DOI: 10.48546/workflowhub.workflow.1246.2

Use Case 11: Related Proteins/Metabolites across DCCs

The workflow starts with selecting RPE as the search term. For the given gene ID (SYMBOL), StringDB PPI was extracted using their API[1]. For the Given StringDB PPI, the list of nodes (Gene Set) is generated. For the Given StringDB PPI, the list of nodes (GeneSet) is generated. Reversers and mimickers from over 1 million signatures were identified using SigCom LINCS[2]. The gene set was submitted to Enrichr[4]. The gene set was then searched in the Metabolomics Workbench[5] to identify relevant ...

Type: Playbook Workflow Builder Workflow

Creator: Playbook Partnership NIH CFDE

Submitter: Daniel Clarke

DOI: 10.48546/workflowhub.workflow.1245.2

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