Similar articles for PMID: 20705737

Year	Number of Results
2008	4
2009	6
2010	15
2011	16
2012	13
2013	16
2014	10
2015	8
2016	6
2017	4
2018	4
2019	4
2020	1
2021	1
2024	0

1

Exome sequencing: the sweet spot before whole genomes.

Teer JK, Mullikin JC. Teer JK, et al. Hum Mol Genet. 2010 Oct 15;19(R2):R145-51. doi: 10.1093/hmg/ddq333. Epub 2010 Aug 12. Hum Mol Genet. 2010. PMID: 20705737 Free PMC article. Review.

2

Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.

Lin X, Tang W, Ahmad S, Lu J, Colby CC, Zhu J, Yu Q. Lin X, et al. Hear Res. 2012 Jun;288(1-2):67-76. doi: 10.1016/j.heares.2012.01.004. Epub 2012 Jan 14. Hear Res. 2012. PMID: 22269275 Free PMC article. Review.

3

Variant detection sensitivity and biases in whole genome and exome sequencing.

Meynert AM, Ansari M, FitzPatrick DR, Taylor MS. Meynert AM, et al. BMC Bioinformatics. 2014 Jul 19;15(1):247. doi: 10.1186/1471-2105-15-247. BMC Bioinformatics. 2014. PMID: 25038816 Free PMC article.

4

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing.

Lee H, O'Connor BD, Merriman B, Funari VA, Homer N, Chen Z, Cohn DH, Nelson SF. Lee H, et al. BMC Genomics. 2009 Dec 31;10:646. doi: 10.1186/1471-2164-10-646. BMC Genomics. 2009. PMID: 20043857 Free PMC article.

5

Whole-exome/genome sequencing and genomics.

Grody WW, Thompson BH, Hudgins L. Grody WW, et al. Pediatrics. 2013 Dec;132(Suppl 3):S211-5. doi: 10.1542/peds.2013-1032E. Pediatrics. 2013. PMID: 24298129

6

Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting.

Teer JK, Johnston JJ, Anzick SL, Pineda M, Stone G; NISC Comparative Sequencing Program; Meltzer PS, Mullikin JC, Biesecker LG. Teer JK, et al. BMC Genomics. 2013 Apr 15;14:253. doi: 10.1186/1471-2164-14-253. BMC Genomics. 2013. PMID: 23586822 Free PMC article.

7

Strategies for exome and genome sequence data analysis in disease-gene discovery projects.

Robinson PN, Krawitz P, Mundlos S. Robinson PN, et al. Clin Genet. 2011 Aug;80(2):127-32. doi: 10.1111/j.1399-0004.2011.01713.x. Epub 2011 Jun 13. Clin Genet. 2011. PMID: 21615730

8

Wessim: a whole-exome sequencing simulator based on in silico exome capture.

Kim S, Jeong K, Bafna V. Kim S, et al. Bioinformatics. 2013 Apr 15;29(8):1076-7. doi: 10.1093/bioinformatics/btt074. Epub 2013 Feb 14. Bioinformatics. 2013. PMID: 23413434 Free PMC article.

9

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.

Teer JK, Bonnycastle LL, Chines PS, Hansen NF, Aoyama N, Swift AJ, Abaan HO, Albert TJ; NISC Comparative Sequencing Program; Margulies EH, Green ED, Collins FS, Mullikin JC, Biesecker LG. Teer JK, et al. Genome Res. 2010 Oct;20(10):1420-31. doi: 10.1101/gr.106716.110. Epub 2010 Sep 1. Genome Res. 2010. PMID: 20810667 Free PMC article.

10

Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.

Carr IM, Morgan J, Watson C, Melnik S, Diggle CP, Logan CV, Harrison SM, Taylor GR, Pena SD, Markham AF, Alkuraya FS, Black GC, Ali M, Bonthron DT. Carr IM, et al. Hum Mutat. 2013 Jul;34(7):945-52. doi: 10.1002/humu.22322. Epub 2013 Apr 29. Hum Mutat. 2013. PMID: 23554237

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