Evidence map›Paper›PMID 31619717›Full record

ArticleScientific reports2019

Scalable Genome Assembly through Parallel de Bruijn Graph Construction for Multiple k-mers.

Kanak Mahadik, Christopher Wright, Milind Kulkarni, Saurabh Bagchi, Somali Chaterji

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The parallelism motifs of genomic data analysis.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2020
    Article
  7. UniqueInternational journal of molecular sciences · 2020
    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.

Kanak MahadikAdobe Research, San Jose, USA. mahadik@adobe.com.
Christopher WrightPurdue University, West Lafayette, IN, USA.ORCID http://orcid.org/0000-0002-2592-0407
Milind KulkarniPurdue University, West Lafayette, IN, USA.
Saurabh BagchiPurdue University, West Lafayette, IN, USA.
Somali ChaterjiPurdue University, West Lafayette, IN, USA. schaterji@schaterji.io.

Funding

U.S. Department of Health & Human Services | NIH | Center for Information Technology (Center for Information Technology, National Institutes of Health) 1R01AI123037
6 · The paper itself

Abstract

Remarkable advancements in high-throughput gene sequencing technologies have led to an exponential growth in the number of sequenced genomes. However, unavailability of highly parallel and scalable de novo assembly algorithms have hindered biologists attempting to swiftly assemble high-quality complex genomes. Popular de Bruijn graph assemblers, such as IDBA-UD, generate high-quality assemblies by iterating over a set of k-values used in the construction of de Bruijn graphs (DBG). However, this process of sequentially iterating from small to large k-values slows down the process of assembly. In this paper, we propose ScalaDBG, which metamorphoses this sequential process, building DBGs for each distinct k-value in parallel. We develop an innovative mechanism to "patch" a higher k-valued graph with contigs generated from a lower k-valued graph. Moreover, ScalaDBG leverages multi-level parallelism, by both scaling up on all cores of a node, and scaling out to multiple nodes simultaneously. We demonstrate that ScalaDBG completes assembling the genome faster than IDBA-UD, but with similar accuracy on a variety of datasets (6.8X faster for one of the most complex genome in our dataset).

Indexed as

AlgorithmsGenomeSoftwareBase SequenceBenchmarkingContig MappingDatasets as TopicEscherichia coliHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNAStaphylococcus aureus

Identifiers

PMID31619717
PMCPMC6795807

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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.