Evidence map›Paper›PMID 29444237›Full record

ArticleBioinformatics (Oxford, England)2018

Compression of genomic sequencing reads via hash-based reordering: algorithm and analysis.

Shubham Chandak, Kedar Tatwawadi, Tsachy Weissman

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. SPRING: a next-generation compressor for FASTQ data.Bioinformatics (Oxford, England) · 2019
    Article
  11. Tackling the Challenges of FASTQ Referential Compression.Bioinformatics and biology insights · 2019
    Article
  12. Article
  13. 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

3 authors.

Shubham ChandakDepartment of Electrical Engineering, Stanford University, Stanford, CA 94305, USA.
Kedar TatwawadiDepartment of Electrical Engineering, Stanford University, Stanford, CA 94305, USA.
Tsachy WeissmanDepartment of Electrical Engineering, Stanford University, Stanford, CA 94305, USA.

Funding

Genomic Compression: From Information Theory to Parallel AlgorithmsU01CA198943 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI MILENKOVIC, OLGICA, WEISSMAN, TSACHY · 2015 to 2017
$1.4M
NCI NIH HHS U01 CA198943
6 · The paper itself

Abstract

Motivation: New Generation Sequencing (NGS) technologies for genome sequencing produce large amounts of short genomic reads per experiment, which are highly redundant and compressible. However, general-purpose compressors are unable to exploit this redundancy due to the special structure present in the data. Results: We present a new algorithm for compressing reads both with and without preserving the read order. In both cases, it achieves 1.4×-2× compression gain over state-of-the-art read compression tools for datasets containing as many as 3 billion Illumina reads. Our tool is based on the idea of approximately reordering the reads according to their position in the genome using hashed substring indices. We also present a systematic analysis of the read compression problem and compute bounds on fundamental limits of read compression. This analysis sheds light on the dynamics of the proposed algorithm (and read compression algorithms in general) and helps understand its performance in practice. The algorithm compresses only the read sequence, works with unaligned FASTQ files, and does not require a reference. Contact: schandak@stanford.edu. Supplementary information: Supplementary material are available at Bioinformatics online. The proposed algorithm is available for download at https://github.com/shubhamchandak94/HARC.

Indexed as

AlgorithmsGenomeBacteriaData CompressionEukaryotaGenomicsHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNASoftware

Identifiers

PMID29444237
PMCPMC5860611

What OpenQuestion holds

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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.