Evidence map›Paper›PMID 20406472›Full record

ArticleBMC bioinformatics2010

Missing value imputation for epistatic MAPs.

Colm Ryan, Derek Greene, Gerard Cagney, Pádraig Cunningham

Abstract read
In one paragraph

Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Data Imputation in Epistatic MAPs by Network-Guided Matrix Completion.Journal of computational biology : a journal of computational molecular cell biology · 2015
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Imputing and predicting quantitative genetic interactions in epistatic MAPs.Methods in molecular biology (Clifton, N.J.) · 2011
    Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Colm RyanSchool of Computer Science and Informatics, University College Dublin, Dublin, Ireland. colm.ryan@ucd.ie
Derek Greene
Gerard Cagney
Pádraig Cunningham

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpistatic miniarray profiling (E-MAPs) is a high-throughput approach capable of quantifying aggravating or alleviating genetic interactions between gene pairs. The datasets resulting from E-MAP experiments typically take the form of a symmetric pairwise matrix of interaction scores. These datasets have a significant number of missing values - up to 35% - that can reduce the effectiveness of some data analysis techniques and prevent the use of others. An effective method for imputing interactions would therefore increase the types of possible analysis, as well as increase the potential to identify novel functional interactions between gene pairs. Several methods have been developed to handle missing values in microarray data, but it is unclear how applicable these methods are to E-MAP data because of their pairwise nature and the significantly larger number of missing values. Here we evaluate four alternative imputation strategies, three local (Nearest neighbor-based) and one global (PCA-based), that have been modified to work with symmetric pairwise data.

resultsWe identify different categories for the missing data based on their underlying cause, and show that values from the largest category can be imputed effectively. We compare local and global imputation approaches across a variety of distinct E-MAP datasets, showing that both are competitive and preferable to filling in with zeros. In addition we show that these methods are effective in an E-MAP from a different species, suggesting that pairwise imputation techniques will be increasingly useful as analogous epistasis mapping techniques are developed in different species. We show that strongly alleviating interactions are significantly more difficult to predict than strongly aggravating interactions. Finally we show that imputed interactions, generated using nearest neighbor methods, are enriched for annotations in the same manner as measured interactions. Therefore our method potentially expands the number of mapped epistatic interactions. In addition we make implementations of our algorithms available for use by other researchers.

conclusionsWe address the problem of missing value imputation for E-MAPs, and suggest the use of symmetric nearest neighbor based approaches as they offer consistently accurate imputations across multiple datasets in a tractable manner.

Indexed as

Epistasis, GeneticAlgorithmsDatabases, GeneticGene Expression ProfilingOligonucleotide Array Sequence Analysis

Identifiers

PMID20406472
PMCPMC2873538

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.