797 related articles for article (PubMed ID: 24919879)
1. Blue: correcting sequencing errors using consensus and context.
Greenfield P; Duesing K; Papanicolaou A; Bauer DC
Bioinformatics; 2014 Oct; 30(19):2723-32. PubMed ID: 24919879
[TBL] [Abstract][Full Text] [Related]
2. QuorUM: An Error Corrector for Illumina Reads.
Marçais G; Yorke JA; Zimin A
PLoS One; 2015; 10(6):e0130821. PubMed ID: 26083032
[TBL] [Abstract][Full Text] [Related]
3. Pollux: platform independent error correction of single and mixed genomes.
Marinier E; Brown DG; McConkey BJ
BMC Bioinformatics; 2015 Jan; 16(1):10. PubMed ID: 25592313
[TBL] [Abstract][Full Text] [Related]
4. Correction of sequencing errors in a mixed set of reads.
Salmela L
Bioinformatics; 2010 May; 26(10):1284-90. PubMed ID: 20378555
[TBL] [Abstract][Full Text] [Related]
5. UNDR ROVER - a fast and accurate variant caller for targeted DNA sequencing.
Park DJ; Li R; Lau E; Georgeson P; Nguyen-Dumont T; Pope BJ
BMC Bioinformatics; 2016 Apr; 17():165. PubMed ID: 27083325
[TBL] [Abstract][Full Text] [Related]
6. A hybrid and scalable error correction algorithm for indel and substitution errors of long reads.
Das AK; Goswami S; Lee K; Park SJ
BMC Genomics; 2019 Dec; 20(Suppl 11):948. PubMed ID: 31856721
[TBL] [Abstract][Full Text] [Related]
7. EC: an efficient error correction algorithm for short reads.
Saha S; Rajasekaran S
BMC Bioinformatics; 2015; 16 Suppl 17(Suppl 17):S2. PubMed ID: 26678663
[TBL] [Abstract][Full Text] [Related]
8. BFC: correcting Illumina sequencing errors.
Li H
Bioinformatics; 2015 Sep; 31(17):2885-7. PubMed ID: 25953801
[TBL] [Abstract][Full Text] [Related]
9. Illumina error correction near highly repetitive DNA regions improves de novo genome assembly.
Heydari M; Miclotte G; Van de Peer Y; Fostier J
BMC Bioinformatics; 2019 Jun; 20(1):298. PubMed ID: 31159722
[TBL] [Abstract][Full Text] [Related]
10. AfterQC: automatic filtering, trimming, error removing and quality control for fastq data.
Chen S; Huang T; Zhou Y; Han Y; Xu M; Gu J
BMC Bioinformatics; 2017 Mar; 18(Suppl 3):80. PubMed ID: 28361673
[TBL] [Abstract][Full Text] [Related]
11. Karect: accurate correction of substitution, insertion and deletion errors for next-generation sequencing data.
Allam A; Kalnis P; Solovyev V
Bioinformatics; 2015 Nov; 31(21):3421-8. PubMed ID: 26177965
[TBL] [Abstract][Full Text] [Related]
12. HISEA: HIerarchical SEed Aligner for PacBio data.
Khiste N; Ilie L
BMC Bioinformatics; 2017 Dec; 18(1):564. PubMed ID: 29258419
[TBL] [Abstract][Full Text] [Related]
13. Correcting errors in short reads by multiple alignments.
Salmela L; Schröder J
Bioinformatics; 2011 Jun; 27(11):1455-61. PubMed ID: 21471014
[TBL] [Abstract][Full Text] [Related]
14. Correcting base-assignment errors in repeat regions of shotgun assembly.
Zhi D; Keich U; Pevzner P; Heber S; Tang H
IEEE/ACM Trans Comput Biol Bioinform; 2007; 4(1):54-64. PubMed ID: 17277413
[TBL] [Abstract][Full Text] [Related]
15. ARAMIS: From systematic errors of NGS long reads to accurate assemblies.
Sacristán-Horcajada E; González-de la Fuente S; Peiró-Pastor R; Carrasco-Ramiro F; Amils R; Requena JM; Berenguer J; Aguado B
Brief Bioinform; 2021 Nov; 22(6):. PubMed ID: 34013348
[TBL] [Abstract][Full Text] [Related]
16. Omega: an overlap-graph de novo assembler for metagenomics.
Haider B; Ahn TH; Bushnell B; Chai J; Copeland A; Pan C
Bioinformatics; 2014 Oct; 30(19):2717-22. PubMed ID: 24947750
[TBL] [Abstract][Full Text] [Related]
17. Correcting short reads with high error rates for improved sequencing result.
Wong TK; Lam TW; Chan PY; Yiu SM
Int J Bioinform Res Appl; 2009; 5(2):224-37. PubMed ID: 19324607
[TBL] [Abstract][Full Text] [Related]
18. Improving the sensitivity of long read overlap detection using grouped short k-mer matches.
Du N; Chen J; Sun Y
BMC Genomics; 2019 Apr; 20(Suppl 2):190. PubMed ID: 30967123
[TBL] [Abstract][Full Text] [Related]
19. CoLoRMap: Correcting Long Reads by Mapping short reads.
Haghshenas E; Hach F; Sahinalp SC; Chauve C
Bioinformatics; 2016 Sep; 32(17):i545-i551. PubMed ID: 27587673
[TBL] [Abstract][Full Text] [Related]
20. Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads.
Wick RR; Judd LM; Gorrie CL; Holt KE
PLoS Comput Biol; 2017 Jun; 13(6):e1005595. PubMed ID: 28594827
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
