Display Settings:


Send to:

Choose Destination
See comment in PubMed Commons below
Genome Inform. 2009 Oct;23(1):189-201.

Recount: expectation maximization based error correction tool for next generation sequencing data.

Author information

  • 1AIST, Computational Biology Research Center, 2-42 Aomi, Koutou-Ku, Tokyo 135-0064, Japan. e-wijaya@aist.go.jp


Next generation sequencing technologies enable rapid, large-scale production of sequence data sets. Unfortunately these technologies also have a non-neglible sequencing error rate, which biases their outputs by introducing false reads and reducing the quantity of the real reads. Although methods developed for SAGE data can reduce these false counts to a considerable degree, until now they have not been implemented in a scalable way. Recently, a program named FREC has been developed to address this problem for next generation sequencing data. In this paper, we introduce RECOUNT, our implementation of an Expectation Maximization algorithm for tag count correction and compare it to FREC. Using both the reference genome and simulated data, we find that RECOUNT performs as well or better than FREC, while using much less memory (e.g. 5GB vs. 75GB). Furthermore, we report the first analysis of tag count correction with real data in the context of gene expression analysis. Our results show that tag count correction not only increases the number of mappable tags, but can make a real difference in the biological interpretation of next generation sequencing data. RECOUNT is an open-source C++ program available at http://seq.cbrc.jp/recount.

[PubMed - indexed for MEDLINE]
Free full text
PubMed Commons home

PubMed Commons

How to join PubMed Commons

    Supplemental Content

    Icon for World Scientific Publishing Company
    Loading ...
    Write to the Help Desk