Mikado
Mikado reconstructs and selects optimal transcript models by integrating multiple RNA sequencing (RNA-seq) assemblies to produce coherent transcript annotations and is implemented in Python3 and Cython.
Key Features:
- Integration of Multiple Assemblies: Combines outputs from various RNA-seq assemblers to leverage complementary strengths and improve transcript reconstruction accuracy.
- Redundancy Removal: Identifies and eliminates redundant transcript models to streamline annotations.
- Optimal Transcript Model Selection: Selects the best transcript models based on user-specified metrics.
- Artifact Resolution: Detects and resolves common artifacts such as erroneous transcript chimerisms.
Scientific Applications:
- Non-model organism transcript annotation: Improves transcript reconstruction accuracy in studies of non-model organisms where assembler performance varies.
- Complex experimental designs: Enhances reliability of reconstructed transcripts across variable aligner and assembler performance in diverse experimental conditions.
- Genomics and transcriptomics research: Produces coherent annotations for downstream analyses requiring accurate and reproducible RNA-seq-derived transcripts.
Methodology:
Integrates multiple RNA-seq assemblies into a coherent transcript annotation by removing redundancies, selecting optimal transcript models based on user-defined criteria, and resolving artifacts such as erroneous chimerisms.
Topics
Collections
Details
- License:
- LGPL-3.0
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- Python
- Added:
- 8/20/2017
- Last Updated:
- 9/4/2019
Operations
Data Inputs & Outputs
Gene prediction
Publications
Venturini L, Caim S, Kaithakottil GG, Mapleson DL, Swarbreck D. Leveraging multiple transcriptome assembly methods for improved gene structure annotation. GigaScience. 2018;7(8). doi:10.1093/gigascience/giy093. PMID:30052957. PMCID:PMC6105091.
PMID: 30052957
PMCID: PMC6105091
Funding: - Biotechnology and Biological Sciences Research Council: BB/CSP1720/1
- BBSRC National Capability in Genomics: BB/CCG1720/1