Pindel
Pindel is a computer program that uses a pattern growth approach to detect breakpoints of large deletions and medium-sized insertions from paired-end short reads. The tool is able to accurately detect indels and long structural variations using both simulated reads and real data. Pindel is freely available for download and comes with a short user manual.
Topic
DNA structural variation
Detail
Operation: Localised reassembly;Read mapping;Split read mapping
Software interface: Command-line user interface
Language: C++
License: GNU General Public License v3.0
Cost: Free
Version name: v0.2.5b8
Credit: NGI/EBI fellowship 050-72-436 from Netherlands Genomics Initiative.
Input: -
Output: -
Contact: Kai Ye k.ye@lumc.nl, Zemin Ning zn1@sanger.ac.uk
Collection: -
Maturity: Stable
Publications
- Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads.
- Ye K, et al. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. 2009; 25:2865-71. doi: 10.1093/bioinformatics/btp394
- https://doi.org/10.1093/bioinformatics/btp394
- PMID: 19561018
- PMC: PMC2781750
Download and documentation
Source: http://gmt.genome.wustl.edu/packages/pindel/install.html
Documentation: http://gmt.genome.wustl.edu/packages/pindel/user-manual.html
Home page: http://gmt.genome.wustl.edu/packages/pindel/
Links: http://gmt.genome.wustl.edu/packages/pindel/quick-start.html
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