Evidence map›Paper›PMID 28831090›Full record

ArticleScientific reports2017

Accelerating next generation sequencing data analysis with system level optimizations.

Nagarajan Kathiresan, Ramzi Temanni, Hakeem Almabrazi, Najeeb Syed, Puthen V Jithesh, Rashid Al-Ali

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
1.0field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Optimized splitting of mixed-species RNA sequencing data.Journal of bioinformatics and computational biology · 2022
    Article
  6. Review
  7. Article
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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 1 institution in 1 country.

Nagarajan KathiresanBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar. nkathiresan@sidra.org.
Ramzi TemanniBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar.
Hakeem AlmabraziBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar.
Najeeb SyedBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar.
Puthen V JitheshBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar.ORCID 0000-0001-7747-0930
Rashid Al-AliBiomedical Informatics, Research Branch, Sidra Medical and Research Center, Post Box No. 26999, Doha, Qatar.
Sidra Medical and Research Center · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next generation sequencing (NGS) data analysis is highly compute intensive. In-memory computing, vectorization, bulk data transfer, CPU frequency scaling are some of the hardware features in the modern computing architectures. To get the best execution time and utilize these hardware features, it is necessary to tune the system level parameters before running the application. We studied the GATK-HaplotypeCaller which is part of common NGS workflows, that consume more than 43% of the total execution time. Multiple GATK 3.x versions were benchmarked and the execution time of HaplotypeCaller was optimized by various system level parameters which included: (i) tuning the parallel garbage collection and kernel shared memory to simulate in-memory computing, (ii) architecture-specific tuning in the PairHMM library for vectorization, (iii) including Java 1.8 features through GATK source code compilation and building a runtime environment for parallel sorting and bulk data transfer (iv) the default 'on-demand' mode of CPU frequency is over-clocked by using 'performance-mode' to accelerate the Java multi-threads. As a result, the HaplotypeCaller execution time was reduced by 82.66% in GATK 3.3 and 42.61% in GATK 3.7. Overall, the execution time of NGS pipeline was reduced to 70.60% and 34.14% for GATK 3.3 and GATK 3.7 respectively.

Indexed as

High-Throughput Nucleotide SequencingSequence Analysis, DNAChromosome MappingComputational BiologyDatabases, GeneticGenomicsGenotyping TechniquesReproducibility of ResultsSoftwareWorkflow

Identifiers

PMID28831090
PMCPMC5567265
OpenAlexW2745359018

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.