Evidence map›Paper›PMID 30020403›Full record

ArticleBioinformatics (Oxford, England)2019

Dynamic compression schemes for graph coloring.

Harun Mustafa, Ingo Schilken, Mikhail Karasikov, Carsten Eickhoff, Gunnar Rätsch, André Kahles

Open access · hybridAbstract 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  3. Data Structures to Represent a Set ofACM computing surveys · 2022
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  4. Succinct dynamic de Bruijn graphs.Bioinformatics (Oxford, England) · 2021
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  5. Topology-based sparsification of graph annotations.Bioinformatics (Oxford, England) · 2021
    Article
  6. Data structures based onGenome research · 2021
    Review
  7. An Efficient, Scalable, and Exact Representation of High-Dimensional Color Information Enabled Using de Bruijn Graph Search.Journal of computational biology : a journal of computational molecular cell biology · 2020
    Article
  8. Sparse Binary Relation Representations for Genome Graph Annotation.Journal of computational biology : a journal of computational molecular cell biology · 2020
    Article
  9. Improved representation of sequence bloom trees.Bioinformatics (Oxford, England) · 2020
    Article
  10. 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

6 authors at 3 institutions in 2 countries.

Harun MustafaDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
Ingo SchilkenDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
Mikhail KarasikovDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
Carsten EickhoffBrown Center for Biomedical Informatics, Brown University, Providence, RI, USA.
Gunnar RätschDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
André KahlesDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
SIB Swiss Institute of Bioinformatics · CHBrown University · USETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Technological advancements in high-throughput DNA sequencing have led to an exponential growth of sequencing data being produced and stored as a byproduct of biomedical research. Despite its public availability, a majority of this data remains hard to query for the research community due to a lack of efficient data representation and indexing solutions. One of the available techniques to represent read data is a condensed form as an assembly graph. Such a representation contains all sequence information but does not store contextual information and metadata. Results: We present two new approaches for a compressed representation of a graph coloring: a lossless compression scheme based on a novel application of wavelet tries as well as a highly accurate lossy compression based on a set of Bloom filters. Both strategies retain a coloring even when adding to the underlying graph topology. We present construction and merge procedures for both methods and evaluate their performance on a wide range of different datasets. By dropping the requirement of a fully lossless compression and using the topological information of the underlying graph, we can reduce memory requirements by up to three orders of magnitude. Representing individual colors as independently stored modules, our approaches can be efficiently parallelized and provide strategies for dynamic use. These properties allow for an easy upscaling to the problem sizes common to the biomedical domain. Availability and implementation: We provide prototype implementations in C++, summaries of our experiments as well as links to all datasets publicly at https://github.com/ratschlab/graph_annotation. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Computational BiologyData CompressionSoftwareAlgorithmsColorGenomicsHigh-Throughput Nucleotide Sequencing

Identifiers

PMID30020403
PMCPMC6530811
OpenAlexW2951157731

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.