Evidence map›Paper›PMID 26139636›Full record

ArticleBioinformatics (Oxford, England)2015

ERGC: an efficient referential genome compression algorithm.

Subrata Saha, Sanguthevar Rajasekaran

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Tackling the Challenges of FASTQ Referential Compression.Bioinformatics and biology insights · 2019
    Article
  6. Article
  7. Article
  8. NRGC: a novel referential genome compression algorithm.Bioinformatics (Oxford, England) · 2016
    Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Subrata SahaDepartment of Computer Science and Engineering, University of Connecticut, Storrs, CT 06269, USA.
Sanguthevar RajasekaranDepartment of Computer Science and Engineering, University of Connecticut, Storrs, CT 06269, USA.

Funding

Efficient Algorithms for Motif SearchR01LM010101 · NLM · UNIVERSITY OF CONNECTICUT STORRS · PI RAJASEKARAN, SANGUTHEVAR · 2010 to 2013
$1.4M
NLM NIH HHS R01-LM010101
6 · The paper itself

Abstract

motivationGenome sequencing has become faster and more affordable. Consequently, the number of available complete genomic sequences is increasing rapidly. As a result, the cost to store, process, analyze and transmit the data is becoming a bottleneck for research and future medical applications. So, the need for devising efficient data compression and data reduction techniques for biological sequencing data is growing by the day. Although there exists a number of standard data compression algorithms, they are not efficient in compressing biological data. These generic algorithms do not exploit some inherent properties of the sequencing data while compressing. To exploit statistical and information-theoretic properties of genomic sequences, we need specialized compression algorithms. Five different next-generation sequencing data compression problems have been identified and studied in the literature. We propose a novel algorithm for one of these problems known as reference-based genome compression.

resultsWe have done extensive experiments using five real sequencing datasets. The results on real genomes show that our proposed algorithm is indeed competitive and performs better than the best known algorithms for this problem. It achieves compression ratios that are better than those of the currently best performing algorithms. The time to compress and decompress the whole genome is also very promising. AVAILABILITY AND IMPLEMENTATION: The implementations are freely available for non-commercial purposes. They can be downloaded from http://engr.uconn.edu/∼rajasek/ERGC.zip. CONTACT: rajasek@engr.uconn.edu.

Indexed as

AlgorithmsGenome, HumanChromosome MappingDatabases, FactualData CompressionGenomicsHigh-Throughput Nucleotide SequencingHumansInformation Storage and RetrievalSequence Analysis, DNA

Identifiers

PMID26139636
PMCPMC4838057

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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.