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HIPred: an integrative approach to predicting haploinsufficient genes

Research output: Contribution to journalArticle

Original languageEnglish
Number of pages7
JournalBioinformatics
Early online date30 Jan 2017
DOIs
StateE-pub ahead of print - 30 Jan 2017

Abstract

Motivation: A major cause of autosomal dominant disease is haploinsufficiency, whereby a single copy of a gene is not sufficient to maintain the normal function of the gene. A large proportion of existing methods for predicting haploinsufficiency incorporate biological networks, e.g. protein-protein interaction networks, that have recently been shown to introduce study bias. As a result, these methods tend to perform best on well studied genes, but underperform on less studied genes. The advent of large genome sequencing consortia, such as the 1,000 genomes project, NHLBI Exome Sequencing Project (ESP) and the Exome Aggregation Consortium (ExAC) creates an urgent need for unbiased haploinsufficiency prediction methods.

Results: Here, we describe a machine learning approach, called HIPred, that integrates genomic and evolutionary information from ENSEMBL, with functional annotations from the Encyclopaedia of DNA Elements (ENCODE) consortium and the NIH Roadmap Epigenomics Project to predict haploinsufficiency, without the study bias described above. We benchmark HIPred using several datasets and show that our unbiased method performs as well as, and in most cases, outperforms existing biased algorithms.

Availability: HIPred scores for all gene identifiers are available at: https://github.com/HAShihab/HIPred.

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via Oxford University Press at https://academic.oup.com/bioinformatics/article-lookup/doi/10.1093/bioinformatics/btx028. Please refer to any applicable terms of use of the publisher.

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