MMR: A tool for read multi-mapper resolution


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Date

2015

Publication Type

Journal Article

ETH Bibliography

yes

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Abstract

Motivation: Mapping high-throughput sequencing data to a reference genome is an essential step for most analysis pipelines aiming at the computational analysis of genome and transcriptome sequencing data. Breaking ties between equally well mapping locations poses a severe problem not only during the alignment phase but also has significant impact on the results of downstream analyses. We present the multi-mapper resolution (MMR) tool that infers optimal mapping locations from the coverage density of other mapped reads. Results: Filtering alignments with MMR can significantly improve the performance of downstream analyses like transcript quantitation and differential testing. We illustrate that the accuracy (Spearman correlation) of transcript quantification increases by 15% when using reads of length 51. In addition, MMR decreases the alignment file sizes by more than 50%, and this leads to a reduced running time of the quantification tool. Our efficient implementation of the MMR algorithm is easily applicable as a post-processing step to existing alignment files in BAM format. Its complexity scales linearly with the number of alignments and requires no further inputs. Availability and implementation: Open source code and documentation are available for download at http://github.com/ratschlab/mmr. Comprehensive testing results and further information can be found at http://bioweb.me/mmr.

Publication status

published

Editor

Book title

Volume

32 (5)

Pages / Article No.

770 - 772

Publisher

Oxford University Press

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Organisational unit

09568 - Rätsch, Gunnar / Rätsch, Gunnar check_circle

Notes

Published online 30 October 2015.

Funding

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