Similar articles for PMID: 26026159

Year	Number of Results
2010	1
2011	5
2012	6
2013	7
2014	10
2015	15
2016	16
2017	8
2018	5
2019	13
2020	11
2021	8
2022	5
2023	2
2024	0

1

Denoising DNA deep sequencing data-high-throughput sequencing errors and their correction.

Laehnemann D, Borkhardt A, McHardy AC. Laehnemann D, et al. Brief Bioinform. 2016 Jan;17(1):154-79. doi: 10.1093/bib/bbv029. Epub 2015 May 29. Brief Bioinform. 2016. PMID: 26026159 Free PMC article.

2

A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis.

Akogwu I, Wang N, Zhang C, Gong P. Akogwu I, et al. Hum Genomics. 2016 Jul 25;10 Suppl 2(Suppl 2):20. doi: 10.1186/s40246-016-0068-0. Hum Genomics. 2016. PMID: 27461106 Free PMC article.

3

A survey of tools for variant analysis of next-generation genome sequencing data.

Pabinger S, Dander A, Fischer M, Snajder R, Sperk M, Efremova M, Krabichler B, Speicher MR, Zschocke J, Trajanoski Z. Pabinger S, et al. Brief Bioinform. 2014 Mar;15(2):256-78. doi: 10.1093/bib/bbs086. Epub 2013 Jan 21. Brief Bioinform. 2014. PMID: 23341494 Free PMC article.

4

Using de novo assembly to identify structural variation of eight complex immune system gene regions.

Zhang JY, Roberts H, Flores DSC, Cutler AJ, Brown AC, Whalley JP, Mielczarek O, Buck D, Lockstone H, Xella B, Oliver K, Corton C, Betteridge E, Bashford-Rogers R, Knight JC, Todd JA, Band G. Zhang JY, et al. PLoS Comput Biol. 2021 Aug 3;17(8):e1009254. doi: 10.1371/journal.pcbi.1009254. eCollection 2021 Aug. PLoS Comput Biol. 2021. PMID: 34343164 Free PMC article.

5

CARE 2.0: reducing false-positive sequencing error corrections using machine learning.

Kallenborn F, Cascitti J, Schmidt B. Kallenborn F, et al. BMC Bioinformatics. 2022 Jun 13;23(1):227. doi: 10.1186/s12859-022-04754-3. BMC Bioinformatics. 2022. PMID: 35698033 Free PMC article.

6

NanoSim: nanopore sequence read simulator based on statistical characterization.

Yang C, Chu J, Warren RL, Birol I. Yang C, et al. Gigascience. 2017 Apr 1;6(4):1-6. doi: 10.1093/gigascience/gix010. Gigascience. 2017. PMID: 28327957 Free PMC article.

7

SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing.

Spinella JF, Mehanna P, Vidal R, Saillour V, Cassart P, Richer C, Ouimet M, Healy J, Sinnett D. Spinella JF, et al. BMC Genomics. 2016 Nov 14;17(1):912. doi: 10.1186/s12864-016-3281-2. BMC Genomics. 2016. PMID: 27842494 Free PMC article.

8

QuorUM: An Error Corrector for Illumina Reads.

Marçais G, Yorke JA, Zimin A. Marçais G, et al. PLoS One. 2015 Jun 17;10(6):e0130821. doi: 10.1371/journal.pone.0130821. eCollection 2015. PLoS One. 2015. PMID: 26083032 Free PMC article.

9

Benchmarking of long-read assemblers for prokaryote whole genome sequencing.

Wick RR, Holt KE. Wick RR, et al. F1000Res. 2019 Dec 23;8:2138. doi: 10.12688/f1000research.21782.4. eCollection 2019. F1000Res. 2019. PMID: 31984131 Free PMC article.

10

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. Sacristán-Horcajada E, et al. Brief Bioinform. 2021 Nov 5;22(6):bbab170. doi: 10.1093/bib/bbab170. Brief Bioinform. 2021. PMID: 34013348 Free PMC article.

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