Search
Home
Pipelines
Resources
Components
Modules
Subworkflows
Configs
Shared configs
Plugins & Actions
nft-utils
setup-nextflow
setup-nf-test
Docs
Community
What's happening
Advisories
Blog
Events
Bytesize Talks
Hackathons
Training
Talks
Weekly Helpdesks
Programs and groups
Special interest groups
In-progress RFCs
Mentorships
Contributors
Shop
new
Connect game 👾
About
About nf-core
nf-core Lore
Stickers
Governance
Marketing
Code of conduct
Publications
Statistics
Join nf-core
Search
Select theme
Light
Dark
System
Select theme
Light
Dark
System
Join nf-core
Join
nf-core
nf-core/
longraredisease
Long read sequencing pipeline to identify variants in patients with neurodevelopmental disorders
Launch version 1.0.0
https://github.com/nf-core/longraredisease
Introduction
Usage
Parameters
Output
Results
Releases
1.0.0
1.0.0
v1.0.0-alpha
Releases
Introduction
Usage
Parameters
Output
Results
Releases
1.0.0
1.0.0
v1.0.0-alpha
Version history
1.0.0
8 days ago
Download .zip
Download .tar.gz
View on GitHub
v1.0.0-alpha
7 months ago
Download .zip
Download .tar.gz
View on GitHub
run with
See the
docs
on how to configure the Seqera Platform CLI.
nf-core
Nextflow
Seqera Platform
subscribers
1
stars
8
last release
8 days ago
last update
8 days ago
included modules
annotsv_annotsv
annotsv_installannotations
bcftools_concat
bcftools_filter
bcftools_index
and 44 more modules
included subworkflows
bam_stats_samtools
contributors
get help
Ask a question on Slack
Open an issue on GitHub