-
Notifications
You must be signed in to change notification settings - Fork 3
/
.nf-core.yml
31 lines (31 loc) · 1006 Bytes
/
.nf-core.yml
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
lint:
files_exist:
- CITATIONS.md
- docs/README.md
- CODE_OF_CONDUCT.md
- .github/ISSUE_TEMPLATE/config.yml
- .github/workflows/awstest.yml
- .github/workflows/awsfulltest.yml
- assets/nf-core-structural_logo_light.png
- docs/images/nf-core-structural_logo_light.png
- docs/images/nf-core-structural_logo_dark.png
nextflow_config:
- manifest.name
- manifest.homePage
files_unchanged:
- LICENSE
- .github/PULL_REQUEST_TEMPLATE.md
- .github/CONTRIBUTING.md
- .github/ISSUE_TEMPLATE/bug_report.yml
- .github/workflows/linting.yml
- assets/email_template.txt
- assets/email_template.html
- docs/README.md
- .prettierignore
actions_ci: false
repository_type: pipeline
template:
author: nvnieuwk
description: A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads.
name: structural
prefix: nf-cmgg