Evidence map›Paper›PMID 29722813›Full record

ArticleGenome biology and evolution2018

IMPUTOR: Phylogenetically Aware Software for Imputation of Errors in Next-Generation Sequencing.

Matthew Jobin, Haiko Schurz, Brenna M Henn

Erratum issuedAbstract readTechnical Report
In one paragraph

Article in Genome biology and evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Matthew JobinDepartment of Anthropology, Santa Clara University.
Haiko SchurzDivision of Molecular Biology and Human Genetics, Stellenbosch University, Tygerberg, South Africa.
Brenna M HennDepartment of Anthropology and the Genome Center, University of California, Davis.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We introduce IMPUTOR, software for phylogenetically aware imputation of missing haploid nonrecombining genomic data. Targeted for next-generation sequencing data, IMPUTOR uses the principle of parsimony to impute data marked as missing due to low coverage. Along with efficiently imputing missing variant genotypes, IMPUTOR is capable of reliably and accurately correcting many nonmissing sites that represent spurious sequencing errors. Tests on simulated data show that IMPUTOR is capable of detecting many induced mutations without making erroneous imputations/corrections, with as many as 95% of missing sites imputed and 81% of errors corrected under optimal conditions. We tested IMPUTOR with human Y-chromosomes from pairs of close relatives and demonstrate IMPUTOR's efficacy in imputing missing and correcting erroneous calls.

Indexed as

AlgorithmsPhylogenySoftwareChromosomes, Human, YGene FrequencyGenome-Wide Association StudyGenomicsHaplotypesHigh-Throughput Nucleotide SequencingHumansMalePolymorphism, Single Nucleotide

Identifiers

PMID29722813
PMCPMC5961346

What OpenQuestion holds

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Registered trials

None linked

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.