Abstract
MOTIVATION: Metagenomes are often characterized by high levels of unknown sequences. Reads derived from known microorganisms can easily be identified and analyzed using fast homology search algorithms and a suitable reference database, but the unknown sequences are often ignored in further analyses, biasing conclusions. Nevertheless, it is possible to use more data in a comparative metagenomic analysis by creating a cross-assembly of all reads, i.e. a single assembly of reads from different samples. Comparative metagenomics studies the interrelationships between metagenomes from different samples. Using an assembly algorithm is a fast and intuitive way to link (partially) homologous reads without requiring a database of reference sequences.
RESULTS: Here, we introduce crAss, a novel bioinformatic tool that enables fast simple analysis of cross-assembly files, yielding distances between all metagenomic sample pairs and an insightful image displaying the similarities.
Original language | English |
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Pages (from-to) | 3225-31 |
Number of pages | 7 |
Journal | Bioinformatics |
Volume | 28 |
Issue number | 24 |
DOIs | |
Publication status | Published - 15 Dec 2012 |
Keywords
- Algorithms
- Computational Biology
- Genome, Viral
- Humans
- Metagenome
- Metagenomics
- Software