Similar articles for PMID: 21627824

Year	Number of Results
1878	1
2006	2
2007	5
2008	18
2009	9
2010	26
2011	62
2012	55
2013	35
2014	25
2015	14
2016	11
2017	8
2018	9
2019	5
2020	7
2021	9
2022	18
2023	8
2024	0

1

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.

Eckel-Passow JE, Atkinson EJ, Maharjan S, Kardia SL, de Andrade M. Eckel-Passow JE, et al. BMC Bioinformatics. 2011 May 31;12:220. doi: 10.1186/1471-2105-12-220. BMC Bioinformatics. 2011. PMID: 21627824 Free PMC article.

2

Evaluation of copy number variation detection for a SNP array platform.

Zhang X, Du R, Li S, Zhang F, Jin L, Wang H. Zhang X, et al. BMC Bioinformatics. 2014 Feb 21;15:50. doi: 10.1186/1471-2105-15-50. BMC Bioinformatics. 2014. PMID: 24555668 Free PMC article.

3

Family-Based Benchmarking of Copy Number Variation Detection Software.

Nutsua ME, Fischer A, Nebel A, Hofmann S, Schreiber S, Krawczak M, Nothnagel M. Nutsua ME, et al. PLoS One. 2015 Jul 21;10(7):e0133465. doi: 10.1371/journal.pone.0133465. eCollection 2015. PLoS One. 2015. PMID: 26197066 Free PMC article.

4

Genome-wide algorithm for detecting CNV associations with diseases.

Xu Y, Peng B, Fu Y, Amos CI. Xu Y, et al. BMC Bioinformatics. 2011 Aug 9;12:331. doi: 10.1186/1471-2105-12-331. BMC Bioinformatics. 2011. PMID: 21827692 Free PMC article.

5

Fast detection of de novo copy number variants from SNP arrays for case-parent trios.

Scharpf RB, Beaty TH, Schwender H, Younkin SG, Scott AF, Ruczinski I. Scharpf RB, et al. BMC Bioinformatics. 2012 Dec 12;13:330. doi: 10.1186/1471-2105-13-330. BMC Bioinformatics. 2012. PMID: 23234608 Free PMC article.

6

HaplotypeCN: copy number haplotype inference with Hidden Markov Model and localized haplotype clustering.

Lin YJ, Chen YT, Hsu SN, Peng CH, Tang CY, Yen TC, Hsieh WP. Lin YJ, et al. PLoS One. 2014 May 21;9(5):e96841. doi: 10.1371/journal.pone.0096841. eCollection 2014. PLoS One. 2014. PMID: 24849202 Free PMC article.

7

Detection of copy number variations in brown and white layers based on genotyping panels with different densities.

Drobik-Czwarno W, Wolc A, Fulton JE, Dekkers JCM. Drobik-Czwarno W, et al. Genet Sel Evol. 2018 Nov 6;50(1):54. doi: 10.1186/s12711-018-0428-4. Genet Sel Evol. 2018. PMID: 30400769 Free PMC article.

8

Identification of Copy Number Variants from SNP Arrays Using PennCNV.

Fang L, Wang K. Fang L, et al. Methods Mol Biol. 2018;1833:1-28. doi: 10.1007/978-1-4939-8666-8_1. Methods Mol Biol. 2018. PMID: 30039360

9

Characterization of copy number variants in a large multibreed population of beef and dairy cattle using high-density single nucleotide polymorphism genotype data.

Rafter P, Purfield DC, Berry DP, Parnell AC, Gormley IC, Kearney JF, Coffey MP, Carthy TR. Rafter P, et al. J Anim Sci. 2018 Sep 29;96(10):4112-4124. doi: 10.1093/jas/sky302. J Anim Sci. 2018. PMID: 30239746 Free PMC article.

10

Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform.

de Andrade M, Atkinson EJ, Bamlet WR, Matsumoto ME, Maharjan S, Slager SL, Vachon CM, Cunningham JM, Kardia SL. de Andrade M, et al. Hum Hered. 2011;71(4):221-33. doi: 10.1159/000328843. Epub 2011 Jul 2. Hum Hered. 2011. PMID: 21734406 Free PMC article.

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