MSIsensor: microsatellite instability detection using paired tumor-normal sequence data

Motivation: Microsatellite instability (MSI) is an important indicator of larger genome instability and has been linked to many genetic diseases, including Lynch syndrome. MSI status is also an independent prognostic factor for favorable survival in multiple cancer types, such as colorectal and endo...

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Published inBioinformatics Vol. 30; no. 7; pp. 1015 - 1016
Main Authors Niu, Beifang, Ye, Kai, Zhang, Qunyuan, Lu, Charles, Xie, Mingchao, McLellan, Michael D., Wendl, Michael C., Ding, Li
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.04.2014
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ISSN1367-4803
1367-4811
1367-4811
1460-2059
DOI10.1093/bioinformatics/btt755

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Summary:Motivation: Microsatellite instability (MSI) is an important indicator of larger genome instability and has been linked to many genetic diseases, including Lynch syndrome. MSI status is also an independent prognostic factor for favorable survival in multiple cancer types, such as colorectal and endometrial. It also informs the choice of chemotherapeutic agents. However, the current PCR–electrophoresis-based detection procedure is laborious and time-consuming, often requiring visual inspection to categorize samples. We developed MSIsensor, a C++ program for automatically detecting somatic microsatellite changes. It computes length distributions of microsatellites per site in paired tumor and normal sequence data, subsequently using these to statistically compare observed distributions in both samples. Comprehensive testing indicates MSIsensor is an efficient and effective tool for deriving MSI status from standard tumor-normal paired sequence data. Availability and implementation:  https://github.com/ding-lab/msisensor Contact:  kye@genome.wustl.edu or lding@genome.wustl.edu Supplementary information:  Supplementary data are available at Bioinformatics online.
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Associate Editor: Micheal Brudno
The authors wish it to be known that, in their opinion, the first two authors should be regarded as Joint First Authors.
ISSN:1367-4803
1367-4811
1367-4811
1460-2059
DOI:10.1093/bioinformatics/btt755