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Multiplex analysis of polyA-linked sequences (MAPS): an RNA-seq strategy to profile poly(A+) RNA
Yu Zhou1, Hai-Ri Li, Jie Huang
1Department of Cellular and Molecular Medicine, Institute for Genomic Medicine, University of California, Room 239, San Diego, La Jolla, CA, 92093-0651, USA.
Methods in Molecular Biology (Clifton, N.J.)
|March 5, 2014
Summary
This study reviews gene expression profiling methods targeting the 3' end of mRNA. It details the MAPS method for cost-effective gene expression analysis and alternative polyadenylation quantification using deep sequencing.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- Gene expression profiling is crucial for understanding cellular function.
- Methods focusing on the 3' end of poly(A+) mRNA offer specific advantages.
- Existing methods vary in complexity, cost, and data output.
Purpose of the Study:
- To review and compare 12 experimental methods for 3'-end mRNA profiling.
- To provide a detailed protocol for the MAPS method.
- To offer guidelines for analyzing MAPS data.
Main Methods:
- Review of 12 gene expression profiling techniques.
- Detailed protocol for the Messenger RNA 3' End Analysis by Sequencing (MAPS) method.
- Deep sequencing and data analysis using the maps3end software package.
Main Results:
- MAPS is presented as a simple, cost-effective method for gene expression profiling.
- MAPS enables quantification of alternative polyadenylation events.
- The method supports library multiplexing for high-throughput analysis.
Conclusions:
- MAPS offers a practical approach to gene expression and alternative polyadenylation analysis.
- The described protocol and analysis guidelines facilitate the adoption of MAPS.
- This work contributes to the advancement of transcriptomic research tools.
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