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Results: 1 to 20 of 422

1.

Comparison of solution-based exome capture methods for next generation sequencing.

Sulonen AM, Ellonen P, Almusa H, Lepistö M, Eldfors S, Hannula S, Miettinen T, Tyynismaa H, Salo P, Heckman C, Joensuu H, Raivio T, Suomalainen A, Saarela J.

Genome Biol. 2011 Sep 28;12(9):R94. doi: 10.1186/gb-2011-12-9-r94.

PMID:
21955854
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Comprehensive comparison of three commercial human whole-exome capture platforms.

Asan, Xu Y, Jiang H, Tyler-Smith C, Xue Y, Jiang T, Wang J, Wu M, Liu X, Tian G, Wang J, Wang J, Yang H, Zhang X.

Genome Biol. 2011 Sep 28;12(9):R95. doi: 10.1186/gb-2011-12-9-r95.

PMID:
21955857
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A comparative analysis of exome capture.

Parla JS, Iossifov I, Grabill I, Spector MS, Kramer M, McCombie WR.

Genome Biol. 2011 Sep 29;12(9):R97. doi: 10.1186/gb-2011-12-9-r97.

PMID:
21958622
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.

Summerer D, Schracke N, Wu H, Cheng Y, Bau S, Stähler CF, Stähler PF, Beier M.

Genomics. 2010 Apr;95(4):241-6. doi: 10.1016/j.ygeno.2010.01.006. Epub 2010 Feb 6.

PMID:
20138981
[PubMed - indexed for MEDLINE]
Free Article
5.

Exome sequencing generates high quality data in non-target regions.

Guo Y, Long J, He J, Li CI, Cai Q, Shu XO, Zheng W, Li C.

BMC Genomics. 2012 May 20;13:194. doi: 10.1186/1471-2164-13-194.

PMID:
22607156
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.

Ramos E, Levinson BT, Chasnoff S, Hughes A, Young AL, Thornton K, Li A, Vallania FL, Province M, Druley TE.

BMC Genomics. 2012 Dec 6;13:683. doi: 10.1186/1471-2164-13-683.

PMID:
23216810
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Comparison of three targeted enrichment strategies on the SOLiD sequencing platform.

Hedges DJ, Guettouche T, Yang S, Bademci G, Diaz A, Andersen A, Hulme WF, Linker S, Mehta A, Edwards YJ, Beecham GW, Martin ER, Pericak-Vance MA, Zuchner S, Vance JM, Gilbert JR.

PLoS One. 2011 Apr 29;6(4):e18595. doi: 10.1371/journal.pone.0018595.

PMID:
21559511
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Exome sequencing of a multigenerational human pedigree.

Hedges DJ, Burges D, Powell E, Almonte C, Huang J, Young S, Boese B, Schmidt M, Pericak-Vance MA, Martin E, Zhang X, Harkins TT, Züchner S.

PLoS One. 2009 Dec 14;4(12):e8232. doi: 10.1371/journal.pone.0008232. Erratum in: PLoS One. 2009;4(12). doi: 10.1371/annotation/b0fe9dd5-16e1-4b50-b590-263518fbd5eb. Hedges, Dale [corrected to Hedges, Dale J].

PMID:
20011588
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.

Bainbridge MN, Wang M, Wu Y, Newsham I, Muzny DM, Jefferies JL, Albert TJ, Burgess DL, Gibbs RA.

Genome Biol. 2011 Jul 25;12(7):R68. doi: 10.1186/gb-2011-12-7-r68.

PMID:
21787409
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Performance of microarray and liquid based capture methods for target enrichment for massively parallel sequencing and SNP discovery.

Kiialainen A, Karlberg O, Ahlford A, Sigurdsson S, Lindblad-Toh K, Syvänen AC.

PLoS One. 2011 Feb 9;6(2):e16486. doi: 10.1371/journal.pone.0016486.

PMID:
21347407
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing.

Boland JF, Chung CC, Roberson D, Mitchell J, Zhang X, Im KM, He J, Chanock SJ, Yeager M, Dean M.

Hum Genet. 2013 Oct;132(10):1153-63. doi: 10.1007/s00439-013-1321-4. Epub 2013 Jun 12.

PMID:
23757002
[PubMed - indexed for MEDLINE]
12.

Comparison of commercially available target enrichment methods for next-generation sequencing.

Bodi K, Perera AG, Adams PS, Bintzler D, Dewar K, Grove DS, Kieleczawa J, Lyons RH, Neubert TA, Noll AC, Singh S, Steen R, Zianni M.

J Biomol Tech. 2013 Jul;24(2):73-86. doi: 10.7171/jbt.13-2402-002.

PMID:
23814499
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Performance comparison of exome DNA sequencing technologies.

Clark MJ, Chen R, Lam HY, Karczewski KJ, Chen R, Euskirchen G, Butte AJ, Snyder M.

Nat Biotechnol. 2011 Sep 25;29(10):908-14. doi: 10.1038/nbt.1975.

PMID:
21947028
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Tissue-specific temporal exome capture revealed muscle-specific genes and SNPs in Indian buffalo (Bubalus bubalis).

Jakhesara SJ, Ahir VB, Padiya KB, Koringa PG, Rank DN, Joshi CG.

Genomics Proteomics Bioinformatics. 2012 Apr;10(2):107-13. doi: 10.1016/j.gpb.2012.05.005. Epub 2012 Jun 12.

PMID:
22768984
[PubMed - indexed for MEDLINE]
Free Article
15.

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.

Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP.

Proc Natl Acad Sci U S A. 2009 Nov 10;106(45):19096-101. doi: 10.1073/pnas.0910672106. Epub 2009 Oct 27.

PMID:
19861545
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

An integrative variant analysis suite for whole exome next-generation sequencing data.

Challis D, Yu J, Evani US, Jackson AR, Paithankar S, Coarfa C, Milosavljevic A, Gibbs RA, Yu F.

BMC Bioinformatics. 2012 Jan 12;13:8. doi: 10.1186/1471-2105-13-8.

PMID:
22239737
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Quantifying single nucleotide variant detection sensitivity in exome sequencing.

Meynert AM, Bicknell LS, Hurles ME, Jackson AP, Taylor MS.

BMC Bioinformatics. 2013 Jun 18;14:195. doi: 10.1186/1471-2105-14-195.

PMID:
23773188
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Imputation-based assessment of next generation rare exome variant arrays.

Martin AR, Tse G, Bustamante CD, Kenny EE.

Pac Symp Biocomput. 2014:241-52.

PMID:
24297551
[PubMed - indexed for MEDLINE]
Free Article
19.

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.

Genome Res. 2010 Oct;20(10):1420-31. doi: 10.1101/gr.106716.110. Epub 2010 Sep 1.

PMID:
20810667
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Annotation-based genome-wide SNP discovery in the large and complex Aegilops tauschii genome using next-generation sequencing without a reference genome sequence.

You FM, Huo N, Deal KR, Gu YQ, Luo MC, McGuire PE, Dvorak J, Anderson OD.

BMC Genomics. 2011 Jan 25;12:59. doi: 10.1186/1471-2164-12-59.

PMID:
21266061
[PubMed - indexed for MEDLINE]
Free PMC Article

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