Literature DB >> 32444882

parSMURF, a high-performance computing tool for the genome-wide detection of pathogenic variants.

Alessandro Petrini1, Marco Mesiti1, Max Schubach2,3, Marco Frasca1, Daniel Danis4, Matteo Re1, Giuliano Grossi1, Luca Cappelletti1, Tiziana Castrignanò5,6, Peter N Robinson4, Giorgio Valentini1,7.   

Abstract

BACKGROUND: Several prediction problems in computational biology and genomic medicine are characterized by both big data as well as a high imbalance between examples to be learned, whereby positive examples can represent a tiny minority with respect to negative examples. For instance, deleterious or pathogenic variants are overwhelmed by the sea of neutral variants in the non-coding regions of the genome: thus, the prediction of deleterious variants is a challenging, highly imbalanced classification problem, and classical prediction tools fail to detect the rare pathogenic examples among the huge amount of neutral variants or undergo severe restrictions in managing big genomic data.
RESULTS: To overcome these limitations we propose parSMURF, a method that adopts a hyper-ensemble approach and oversampling and undersampling techniques to deal with imbalanced data, and parallel computational techniques to both manage big genomic data and substantially speed up the computation. The synergy between Bayesian optimization techniques and the parallel nature of parSMURF enables efficient and user-friendly automatic tuning of the hyper-parameters of the algorithm, and allows specific learning problems in genomic medicine to be easily fit. Moreover, by using MPI parallel and machine learning ensemble techniques, parSMURF can manage big data by partitioning them across the nodes of a high-performance computing cluster. Results with synthetic data and with single-nucleotide variants associated with Mendelian diseases and with genome-wide association study hits in the non-coding regions of the human genome, involhing millions of examples, show that parSMURF achieves state-of-the-art results and an 80-fold speed-up with respect to the sequential version.
CONCLUSIONS: parSMURF is a parallel machine learning tool that can be trained to learn different genomic problems, and its multiple levels of parallelization and high scalability allow us to efficiently fit problems characterized by big and imbalanced genomic data. The C++ OpenMP multi-core version tailored to a single workstation and the C++ MPI/OpenMP hybrid multi-core and multi-node parSMURF version tailored to a High Performance Computing cluster are both available at https://github.com/AnacletoLAB/parSMURF.
© The Author(s) 2020. Published by Oxford University Press.

Entities:  

Keywords:  GWAS; Mendelian diseases; ensemble methods; high-performance computing; high-performance computing tool for genomic medicine; machine learning for genomic medicine; machine learning for imbalanced genomic data; parallel machine learning tool for big data; parallel machine learning tool for imbalanced data; prediction of deleterious or pathogenic variants

Year:  2020        PMID: 32444882      PMCID: PMC7244787          DOI: 10.1093/gigascience/giaa052

Source DB:  PubMed          Journal:  Gigascience        ISSN: 2047-217X            Impact factor:   6.524


  33 in total

1.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

2.  DANN: a deep learning approach for annotating the pathogenicity of genetic variants.

Authors:  Daniel Quang; Yifei Chen; Xiaohui Xie
Journal:  Bioinformatics       Date:  2014-10-22       Impact factor: 6.937

3.  Jannovar: a java library for exome annotation.

Authors:  Marten Jäger; Kai Wang; Sebastian Bauer; Damian Smedley; Peter Krawitz; Peter N Robinson
Journal:  Hum Mutat       Date:  2014-04-09       Impact factor: 4.878

Review 4.  Towards precision medicine.

Authors:  Euan A Ashley
Journal:  Nat Rev Genet       Date:  2016-08-16       Impact factor: 53.242

5.  The 100 000 Genomes Project: bringing whole genome sequencing to the NHS.

Authors:  Clare Turnbull; Richard H Scott; Ellen Thomas; Louise Jones; Nirupa Murugaesu; Freya Boardman Pretty; Dina Halai; Emma Baple; Clare Craig; Angela Hamblin; Shirley Henderson; Christine Patch; Amanda O'Neill; Katherine Smith; Antonio Rueda Martin; Alona Sosinsky; Ellen M McDonagh; Razvan Sultana; Michael Mueller; Damian Smedley; Adam Toms; Lisa Dinh; Tom Fowler; Mark Bale; Tim Hubbard; Augusto Rendon; Sue Hill; Mark J Caulfield
Journal:  BMJ       Date:  2018-04-24

6.  A method to predict the impact of regulatory variants from DNA sequence.

Authors:  Dongwon Lee; David U Gorkin; Maggie Baker; Benjamin J Strober; Alessandro L Asoni; Andrew S McCallion; Michael A Beer
Journal:  Nat Genet       Date:  2015-06-15       Impact factor: 38.330

7.  Functional annotation of noncoding sequence variants.

Authors:  Graham R S Ritchie; Ian Dunham; Eleftheria Zeggini; Paul Flicek
Journal:  Nat Methods       Date:  2014-02-02       Impact factor: 28.547

8.  Imbalance-Aware Machine Learning for Predicting Rare and Common Disease-Associated Non-Coding Variants.

Authors:  Max Schubach; Matteo Re; Peter N Robinson; Giorgio Valentini
Journal:  Sci Rep       Date:  2017-06-07       Impact factor: 4.379

9.  NCBoost classifies pathogenic non-coding variants in Mendelian diseases through supervised learning on purifying selection signals in humans.

Authors:  Barthélémy Caron; Yufei Luo; Antonio Rausell
Journal:  Genome Biol       Date:  2019-02-11       Impact factor: 13.583

10.  Regulatory variants: from detection to predicting impact.

Authors:  Elena Rojano; Pedro Seoane; Juan A G Ranea; James R Perkins
Journal:  Brief Bioinform       Date:  2018-06-08       Impact factor: 11.622

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  1 in total

1.  Interpretable prioritization of splice variants in diagnostic next-generation sequencing.

Authors:  Daniel Danis; Julius O B Jacobsen; Leigh C Carmody; Michael A Gargano; Julie A McMurry; Ayushi Hegde; Melissa A Haendel; Giorgio Valentini; Damian Smedley; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2021-07-21       Impact factor: 11.025

  1 in total

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