Literature DB >> 23853064

RACER: Rapid and accurate correction of errors in reads.

Lucian Ilie1, Michael Molnar.   

Abstract

MOTIVATION: High-throughput next-generation sequencing technologies enable increasingly fast and affordable sequencing of genomes and transcriptomes, with a broad range of applications. The quality of the sequencing data is crucial for all applications. A significant portion of the data produced contains errors, and ever more efficient error correction programs are needed.
RESULTS: We propose RACER (Rapid and Accurate Correction of Errors in Reads), a new software program for correcting errors in sequencing data. RACER has better error-correcting performance than existing programs, is faster and requires less memory. To support our claims, we performed extensive comparison with the existing leading programs on a variety of real datasets. AVAILABILITY: RACER is freely available for non-commercial use at www.csd.uwo.ca/∼ilie/RACER/.

Mesh:

Year:  2013        PMID: 23853064     DOI: 10.1093/bioinformatics/btt407

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  26 in total

1.  Quality score compression improves genotyping accuracy.

Authors:  Y William Yu; Deniz Yorukoglu; Jian Peng; Bonnie Berger
Journal:  Nat Biotechnol       Date:  2015-03       Impact factor: 54.908

Review 2.  From next-generation resequencing reads to a high-quality variant data set.

Authors:  S P Pfeifer
Journal:  Heredity (Edinb)       Date:  2016-10-19       Impact factor: 3.821

3.  Traversing the k-mer Landscape of NGS Read Datasets for Quality Score Sparsification.

Authors:  Y William Yu; Deniz Yorukoglu; Bonnie Berger
Journal:  Res Comput Mol Biol       Date:  2014-04

4.  Pluribus-Exploring the Limits of Error Correction Using a Suffix Tree.

Authors:  Daniel Savel; Thomas LaFramboise; Ananth Grama; Mehmet Koyuturk
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2016-06-29       Impact factor: 3.710

5.  Frequent loss of heterozygosity in CRISPR-Cas9-edited early human embryos.

Authors:  Gregorio Alanis-Lobato; Jasmin Zohren; Afshan McCarthy; Norah M E Fogarty; Nada Kubikova; Emily Hardman; Maria Greco; Dagan Wells; James M A Turner; Kathy K Niakan
Journal:  Proc Natl Acad Sci U S A       Date:  2021-04-09       Impact factor: 11.205

6.  QuorUM: An Error Corrector for Illumina Reads.

Authors:  Guillaume Marçais; James A Yorke; Aleksey Zimin
Journal:  PLoS One       Date:  2015-06-17       Impact factor: 3.240

7.  Indexing Arbitrary-Length k-Mers in Sequencing Reads.

Authors:  Tomasz Kowalski; Szymon Grabowski; Sebastian Deorowicz
Journal:  PLoS One       Date:  2015-07-16       Impact factor: 3.240

8.  VariantMetaCaller: automated fusion of variant calling pipelines for quantitative, precision-based filtering.

Authors:  András Gézsi; Bence Bolgár; Péter Marx; Peter Sarkozy; Csaba Szalai; Péter Antal
Journal:  BMC Genomics       Date:  2015-10-28       Impact factor: 3.969

Review 9.  Analysis of plant microbe interactions in the era of next generation sequencing technologies.

Authors:  Claudia Knief
Journal:  Front Plant Sci       Date:  2014-05-21       Impact factor: 5.753

10.  EC: an efficient error correction algorithm for short reads.

Authors:  Subrata Saha; Sanguthevar Rajasekaran
Journal:  BMC Bioinformatics       Date:  2015-12-07       Impact factor: 3.169

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