Literature DB >> 28549074

CWDPRNP: a tool for cervid prion sequence analysis in program R.

William L Miller1, W David Walter2.   

Abstract

SUMMARY: Chronic wasting disease is a fatal, neurological disease caused by an infectious prion protein, which affects economically and ecologically important members of the family Cervidae. Single nucleotide polymorphisms within the prion protein gene have been linked to differential susceptibility to the disease in many species. Wildlife managers are seeking to determine the frequencies of disease-associated alleles and genotypes and delineate spatial genetic patterns. The CWDPRNP package, implemented in program R, provides a unified framework for analyzing prion protein gene variability and spatial structure.
AVAILABILITY AND IMPLEMENTATION: The CWDPRNP package, manual and example data files are available at http://ecosystems.psu.edu/research/labs/walter-lab/additional-labs/population-genetics-lab. This package is available for all commonly used platforms. CONTACT: wlm159psu@gmail.com. Published by Oxford University Press 2017. This work is written by US Government employees and are in the public domain in the US.

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Year:  2017        PMID: 28549074     DOI: 10.1093/bioinformatics/btx333

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  2 in total

1.  Spatial heterogeneity of prion gene polymorphisms in an area recently infected by chronic wasting disease.

Authors:  William L Miller; W David Walter
Journal:  Prion       Date:  2019-01       Impact factor: 3.931

2.  Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease.

Authors:  Alberto F Fameli; Jessie Edson; Jeremiah E Banfield; Christopher S Rosenberry; W David Walter
Journal:  Prion       Date:  2022-12       Impact factor: 2.547

  2 in total

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