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

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

Documentation