A GUI for Dual and Bulk RNA-Sequencing Analysis
Overview
A 'shiny' app that supports both dual and bulk RNA-seq, with the dual RNA-seq functionality offering the flexibility to perform either a sequential approach (where reads are mapped separately to each genome) or a combined approach (where reads are aligned to a single merged genome). The user-friendly interface automates the analysis process, providing step-by-step guidance, making it easy for users to navigate between different analysis steps, and download intermediate results and publication-ready plots.
Install
Health
- OK13 OK2026-08-23
- ERROR12 OK, 1 ERROR2026-08-22
- OK13 OK2026-08-05
- NOTE12 OK, 1 NOTE2026-08-01
- OK13 OK2026-06-09
Show 3 earlier changesHide 3 earlier changes
- ERROR12 OK, 1 ERROR2026-06-08
- OK12 OK2026-04-25
- NOTE12 OK, 2 NOTE2026-03-10
Documentation
- Help pages
- 66
- Examples that run
- no examples
- Exported functions with examples
- 0%
- Documented parameters
- not tracked
- Return-value docs
- 100%
- Help pages citing references
- 0%
Downloads
Repository
- PRs merged (all time)
- 0%
- Median days to close, 50 most recently updated closed issues
- 61
- Median days to close, 50 most recently updated closed PRs
- 57
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1 development-tooling and community-health practice detected across 1 family in the upstream repository
Checks run against github.com/indagoverse/indago on 2026-10-22.
Dependencies
Installing inDAGO adds 138 packages (64 with compiled code, 122 MB of source tarballs). Heaviest: stringi 11 MB, ggplot2 6.0 MB, data.table 5.7 MB.
Code & Tests
People & History
Package metadata
- First published
- 2025-07-05
- Total releases
- 5 / 1 yrs
- License
- GPL (>= 3) OSI
- Download size
- 441 KB
Cite
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