Paiva's Adaptive Window Heuristic Applied to the PRNP Variant Scanner: Rapid Computational Screening of Pathogenic PRNP Variants by Rabin-Karp Algorithm with Polynomial Hash over a Prime Field.

Human prion diseases, particularly Creutzfeldt-Jakob Disease (CJD), are characterized by rapid progression and a narrow therapeutic window. A documented mean diagnostic delay of 7.8 months - exceeding the median survival of 4 to 6 months - compromises patient eligibility for active clinical trials requiring early-stage disease. This paper describes the development of a computational proof-of-concept tool termed PRNP Variant Scanner, which applies the Rabin-Karp rolling hash algorithm and Paiva's Adaptive Window Heuristic to perform simultaneous multi-pattern screening of 16 pathogenic or clinically relevant variants of the human prion protein gene (PRNP). The approach detects variants in under 1 ms on sequences up to 759 bp, with a mathematically zero false-positive rate, and delivers integrated clinical interpretation including codon 129 haplotype status and eligibility information for the PRISM (NCT07444580) and PrProfile (NCT06153966) clinical trials.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-08-24
DOI
https://doi.org/10.5281/zenodo.22076293
Primary Topic
Prion Diseases and Protein Misfolding
Type
article
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article

Paiva's Adaptive Window Heuristic Applied to the PRNP Variant Scanner: Rapid Computational Screening of Pathogenic PRNP Variants by Rabin-Karp Algorithm with Polynomial Hash over a Prime Field.

Josenildo Paiva
Zenodo (CERN European Organization for Nuclear Research)
Prion Diseases and Protein Misfolding
article

Paiva's Adaptive Window Heuristic Applied to the PRNP Variant Scanner: Rapid Computational Screening of Pathogenic PRNP Variants by Rabin-Karp Algorithm with Polynomial Hash over a Prime Field.

Josenildo Paiva
article en

Abstract

Human prion diseases, particularly Creutzfeldt-Jakob Disease (CJD), are characterized by rapid progression and a narrow therapeutic window. A documented mean diagnostic delay of 7.8 months - exceeding the median survival of 4 to 6 months - compromises patient eligibility for active clinical trials requiring early-stage disease. This paper describes the development of a computational proof-of-concept tool termed PRNP Variant Scanner, which applies the Rabin-Karp rolling hash algorithm and Paiva's Adaptive Window Heuristic to perform simultaneous multi-pattern screening of 16 pathogenic or clinically relevant variants of the human prion protein gene (PRNP). The approach detects variants in under 1 ms on sequences up to 759 bp, with a mathematically zero false-positive rate, and delivers integrated clinical interpretation including codon 129 haplotype status and eligibility information for the PRISM (NCT07444580) and PrProfile (NCT06153966) clinical trials.

Zenodo (CERN European Organization for Nuclear Research)
Centro Universitário Claretiano (BR)
Openalex Percentile: Top 17%
Prion Diseases and Protein Misfolding
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