nQuire specifications

Information


Unique identifier OMICS_18667
Name nQuire
Software type Package/Module
Interface Command line interface
Restrictions to use None
Input format BAM
Output format BIN
Operating system Unix/Linux
Programming languages C
License MIT License
Computer skills Advanced
Stability Stable
Maintained Yes

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Versioning


No version available

Maintainers


  • person_outline Hernan Burbano
  • person_outline Clemens Weiss
  • person_outline Marina Pais
  • person_outline Liliana Cano
  • person_outline Sophien Kamoun

Publication for nQuire

nQuire citation

library_books

Inferring Variation in Copy Number Using High Throughput Sequencing Data in R

2018
Front Genet
PMCID: 5909048
PMID: 29706990
DOI: 10.3389/fgene.2018.00123

[…] is uniform component in an attempt to capture the noise in the data leaving the putatively cleaner data for their Gaussian mixture model. Their software is available on GitHub in the repository named nQuire.The method presented has been designed to work with VCF data () that contains the number of times each allele was sequenced for each variant. In theory, any method that produces a valid VCF fil […]

nQuire institution(s)
Research Group for Ancient Genomics and Evolution, Department of Molecular Biology, Max Planck Institute for Developmental Biology, Tuebingen, Germany; The Sainsbury Laboratory, Norwich, UK; University of Florida, Department of Plant Pathology, Indian River Research and Education Center, Fort Pierce, FL, USA
nQuire funding source(s)
Supported by Presidential Innovation Fund of the Max Planck Society.

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