GATK PathSeq: a customizable computational tool for the discovery and identification of microbial sequences in libraries from eukaryotic hosts
Abstract Summary We present an updated version of our computational pipeline, PathSeq, for the discovery and identification of microbial sequences in genomic and transcriptomic libraries from eukaryotic hosts. This pipeline is available in the Genome Analysis Toolkit (GATK) as a suite of configurabl...
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| Veröffentlicht in: | Bioinformatics Jg. 34; H. 24; S. 4287 - 4289 |
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| Hauptverfasser: | , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
England
Oxford University Press
15.12.2018
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| Schlagworte: | |
| ISSN: | 1367-4803, 1367-4811, 1460-2059, 1367-4811 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Abstract
Summary
We present an updated version of our computational pipeline, PathSeq, for the discovery and identification of microbial sequences in genomic and transcriptomic libraries from eukaryotic hosts. This pipeline is available in the Genome Analysis Toolkit (GATK) as a suite of configurable tools that can report the microbial composition of DNA or RNA short-read sequencing samples and identify unknown sequences for downstream assembly of novel organisms. GATK PathSeq enables sample analysis in minutes at low cost. In addition, these tools are built with the GATK engine and Apache Spark framework, providing robust, rapid parallelization of read quality filtering, host subtraction and microbial alignment in workstation, cluster and cloud environments.
Availability and implementation
These tools are available as a part of the GATK at https://github.com/broadinstitute/gatk.
Supplementary information
Supplementary data are available at Bioinformatics online. |
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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors wish it to be known that, in their opinion, the Mark A.Walker and Chandra Sekhar Pedamallu authors should be regarded as Joint First Authors. |
| ISSN: | 1367-4803 1367-4811 1460-2059 1367-4811 |
| DOI: | 10.1093/bioinformatics/bty501 |