Evidence map›Paper›PMID 30010790›Full record

ArticleBioinformatics (Oxford, England)2019

Metagenomic binning through low-density hashing.

Yunan Luo, Yun William Yu, Jianyang Zeng, Bonnie Berger, Jian Peng

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
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  4. Review
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  12. Sequre: a high-performance framework for rapid development of secure bioinformatics pipelines.IEEE International Symposium on Parallel & Distributed Processing, Workshops and Phd Forum : [proceedings]. IEEE International Symposium on Parallel & Distributed Processing, Workshops and Phd Forum
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yunan LuoDepartment of Computer Science, University of Illinois at Urbana-Champaign, Champaign, IL, USA.
Yun William YuDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Jianyang ZengMachine Learning and Computational Biology Group, Institute for Interdisciplinary Information Sciences, Tsinghua University, Beijing, China and.
Bonnie BergerDepartment of Mathematics and Computer Science and AI Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Jian PengDepartment of Computer Science, University of Illinois at Urbana-Champaign, Champaign, IL, USA.

Funding

Compressive genomics for large omics data sets: Algorithms applications & toolsR01GM108348 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BERGER, BONNIE · 2013 to 2019
$2.1M
6 · The paper itself

Abstract

Motivation: Vastly greater quantities of microbial genome data are being generated where environmental samples mix together the DNA from many different species. Here, we present Opal for metagenomic binning, the task of identifying the origin species of DNA sequencing reads. We introduce 'low-density' locality sensitive hashing to bioinformatics, with the addition of Gallager codes for even coverage, enabling quick and accurate metagenomic binning. Results: On public benchmarks, Opal halves the error on precision/recall (F1-score) as compared with both alignment-based and alignment-free methods for species classification. We demonstrate even more marked improvement at higher taxonomic levels, allowing for the discovery of novel lineages. Furthermore, the innovation of low-density, even-coverage hashing should itself prove an essential methodological advance as it enables the application of machine learning to other bioinformatic challenges. Availability and implementation: Full source code and datasets are available at http://opal.csail.mit.edu and https://github.com/yunwilliamyu/opal. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsGenome, MicrobialMetagenomicsSoftwareComputational BiologySequence Analysis, DNA

Identifiers

PMID30010790
PMCPMC6330020

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Registered trials

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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.