pRESTO
pRESTO is a computational pipeline developed to process high-throughput sequencing reads from lymphocyte receptor studies. It produces error-corrected, sorted, and annotated sequence sets and provides metrics at each step. pRESTO supports multiplexed primer pools, single- or paired-end reads, and single-molecule identifier technologies. The software can efficiently process millions of sequences, and it has been tested on data generated by Roche and Illumina platforms. pRESTO is freely available for academic use.
Topic
Sequencing;DNA;Immunology
Detail
Operation: Nucleic acid sequence analysis
Software interface: Command-line user interface
Language: Python
License: GNU Affero General Public License v3
Cost: Free
Version name: 0.7.1
Credit: National Library of Medicine, United States-Israel Binational Science Foundation, National Institutes of Health, EMD-Merck-Serono sponsored Grant for Multiple Sclerosis Research Innovation; Race to Erase MS.
Input: -
Output: -
Contact: Steven H. Kleinstein steven.kleinstein@yale.edu
Collection: -
Maturity: -
Publications
- pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires.
- Vander Heiden JA, et al. pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires. pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires. 2014; 30:1930-2. doi: 10.1093/bioinformatics/btu138
- https://doi.org/10.1093/bioinformatics/btu138
- PMID: 24618469
- PMC: PMC4071206
Download and documentation
Documentation: https://presto.readthedocs.io/en/latest/
Home page: http://presto.readthedocs.io/en/latest/
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