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Olorin | Combining gene flow with exome sequencing in large family studies of complex disease

An interactive filtering tool for next generation sequencing data coming from the study of large complex disease pedigrees. Olorin is a tool which integrates gene flow output from Merlin and next generation sequencing data. Users can interactively filter and prioritize variants based on haplotype sharing across different sets of selected individuals and allele frequency in reference datasets.

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Olorin forum

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Olorin classification

  • Animals
    • Homo sapiens

Olorin specifications

Unique identifier:
OMICS_01556
Interface:
Command line interface, Graphical user interface
Operating system:
Unix/Linux, Mac OS, Windows
License:
MIT License
Stability:
Stable
Software type:
Package/Module
Restrictions to use:
None
Programming languages:
Java
Computer skills:
Advanced
Maintained:
Yes

Olorin distribution

versioning

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No versioning.

Olorin support

Maintainer

  • James A. Morris <>

Credits

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Publications

Institution(s)

Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK

Funding source(s)

Wellcome Trust grant number WT098051

By using OMICtools you acknowledge that you have read and accepted the terms of the end user license agreement.