Predicting haplogroups using a versatile machine learning program (PredYMaLe) on a new mutationally balanced 32 Y-STR multiplex (CombYplex): Unlocking the full potential of the human STR mutation rate spectrum to estimate forensic parameters

Caroline Bouakaze, Franklin Delehelle, Nancy Saenz-Oyhéréguy, Andreia Moreira, Stéphanie Schiavinato, Myriam Croze, Solène Delon, Cesar Fortes-Lima, Morgane Gibert, Louis Bujan, Eric Huyghe, Gil Bellis, Rosario Calderon, Candela Lucia Hernández, Efren Avendaño-Tamayo, Gabriel Bedoya, Antonio Salas, Stéphane Mazières, Jacques Charioni, Florence Migot-NabiasAndres Ruiz-Linares, Jean-Michel Dugoujon, Catherine Thèves, Catherine Mollereau-Manaute, Camille Noûs, Nicolas Poulet, Turi King, Maria Eugenia D'Amato, Patricia Balaresque

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14 Citations (SciVal)

Abstract

We developed a new mutationally well-balanced 32 Y-STR multiplex (CombYplex) together with a machine learning (ML) program PredYMaLe to assess the impact of STR mutability on haplogourp prediction, while respecting forensic community criteria (high DC/HD). We designed CombYplex around two sub-panels M1 and M2 characterized by average and high-mutation STR panels. Using these two sub-panels, we tested how our program PredYmale reacts to mutability when considering basal branches and, moving down, terminal branches. We tested first the discrimination capacity of CombYplex on 996 human samples using various forensic and statistical parameters and showed that its resolution is sufficient to separate haplogroup classes. In parallel, PredYMaLe was designed and used to test whether a ML approach can predict haplogroup classes from Y-STR profiles. Applied to our kit, SVM and Random Forest classifiers perform very well (average 97 %), better than Neural Network (average 91 %) and Bayesian methods (< 90 %). We observe heterogeneity in haplogroup assignation accuracy among classes, with most haplogroups having high prediction scores (99-100 %) and two (E1b1b and G) having lower scores (67 %). The small sample sizes of these classes explain the high tendency to misclassify the Y-profiles of these haplogroups; results were measurably improved as soon as more training data were added. We provide evidence that our ML approach is a robust method to accurately predict haplogroups when it is combined with a sufficient number of markers, well-balanced mutation rate Y-STR panels, and large ML training sets. Further research on confounding factors (such as CNV-STR or gene conversion) and ideal STR panels in regard to the branches analysed can be developed to help classifiers further optimize prediction scores.

Original languageEnglish
Pages (from-to)102342
JournalForensic Science International. Genetics
Volume48
Early online date29 Jun 2020
DOIs
Publication statusPublished - 30 Sept 2020

Bibliographical note

Copyright © 2020 Elsevier B.V. All rights reserved.

Keywords

  • Chromosomes, Human, Y
  • DNA Fingerprinting
  • Forensic Genetics/methods
  • Haplotypes
  • Humans
  • Machine Learning
  • Male
  • Microsatellite Repeats
  • Multiplex Polymerase Chain Reaction
  • Mutation Rate
  • Polymorphism, Single Nucleotide

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