Detection of colinear blocks and synteny and evolutionary analyses based on utilization of MCScanX.
Yupeng WangHaibao TangXiyin WangYing SunPaule V JosephAndrew H PatersonPublished in: Nature protocols (2024)
As different taxa evolve, gene order often changes slowly enough that chromosomal 'blocks' with conserved gene orders (synteny) are discernible. The MCScanX toolkit ( https://github.com/wyp1125/MCScanX ) was published in 2012 as freely available software for the detection of such 'colinear blocks' and subsequent synteny and evolutionary analyses based on genome-wide gene location and protein sequence information. Owing to its simplicity and high efficiency for colinear block detection, MCScanX provides a powerful tool for conducting diverse synteny and evolutionary analyses. Moreover, the detection of colinear blocks has been embraced as an integral step for pangenome graph construction. Here, new application trends of MCScanX are explored, striving to better connect this increasingly used tool to other tools and accelerate insight generation from exponentially growing sequence data. We provide a detailed protocol that covers how to install MCScanX on diverse platforms, tune parameters, prepare input files from data from the National Center for Biotechnology Information, run MCScanX and its visualization and evolutionary analysis tools, and connect MCScanX with external tools, including MCScanX-transposed, Circos and SynVisio. This protocol is easily implemented by users with minimal computational background and is adaptable to new data of interest to them. The data and utility programs for this protocol can be obtained from http://bdx-consulting.com/mcscanx-protocol .
Keyphrases
- genome wide
- copy number
- dna methylation
- electronic health record
- randomized controlled trial
- loop mediated isothermal amplification
- big data
- label free
- real time pcr
- high efficiency
- data analysis
- gene expression
- healthcare
- health information
- quality improvement
- machine learning
- genome wide identification
- small molecule
- protein protein
- electron microscopy