274 related articles for article (PubMed ID: 21554453)
1. Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling.
Marroni F; Pinosio S; Di Centa E; Jurman I; Boerjan W; Felice N; Cattonaro F; Morgante M
Plant J; 2011 Aug; 67(4):736-45. PubMed ID: 21554453
[TBL] [Abstract][Full Text] [Related]
2. Identification of EMS-induced causal mutations in a non-reference Arabidopsis thaliana accession by whole genome sequencing.
Uchida N; Sakamoto T; Kurata T; Tasaka M
Plant Cell Physiol; 2011 Apr; 52(4):716-22. PubMed ID: 21398646
[TBL] [Abstract][Full Text] [Related]
3. Identification of causal sequence variants of disease in the next generation sequencing era.
Kingsley CB
Methods Mol Biol; 2011; 700():37-46. PubMed ID: 21204025
[TBL] [Abstract][Full Text] [Related]
4. High-resolution genetic mapping of allelic variants associated with cell wall chemistry in Populus.
Muchero W; Guo J; DiFazio SP; Chen JG; Ranjan P; Slavov GT; Gunter LE; Jawdy S; Bryan AC; Sykes R; Ziebell A; Klápště J; Porth I; Skyba O; Unda F; El-Kassaby YA; Douglas CJ; Mansfield SD; Martin J; Schackwitz W; Evans LM; Czarnecki O; Tuskan GA
BMC Genomics; 2015 Jan; 16(1):24. PubMed ID: 25613058
[TBL] [Abstract][Full Text] [Related]
5. Population genomic analysis of Tunisian Medicago truncatula reveals candidates for local adaptation.
Friesen ML; Cordeiro MA; Penmetsa RV; Badri M; Huguet T; Aouani ME; Cook DR; Nuzhdin SV
Plant J; 2010 Aug; 63(4):623-35. PubMed ID: 20545888
[TBL] [Abstract][Full Text] [Related]
6. SNP discovery in black cottonwood (Populus trichocarpa) by population transcriptome resequencing.
Geraldes A; Pang J; Thiessen N; Cezard T; Moore R; Zhao Y; Tam A; Wang S; Friedmann M; Birol I; Jones SJ; Cronk QC; Douglas CJ
Mol Ecol Resour; 2011 Mar; 11 Suppl 1():81-92. PubMed ID: 21429165
[TBL] [Abstract][Full Text] [Related]
7. A new expectation-maximization statistical test for case-control association studies considering rare variants obtained by high-throughput sequencing.
Gordon D; Finch SJ; De La Vega FM
Hum Hered; 2011; 71(2):113-25. PubMed ID: 21734402
[TBL] [Abstract][Full Text] [Related]
8. Design of association studies with pooled or un-pooled next-generation sequencing data.
Kim SY; Li Y; Guo Y; Li R; Holmkvist J; Hansen T; Pedersen O; Wang J; Nielsen R
Genet Epidemiol; 2010 Jul; 34(5):479-91. PubMed ID: 20552648
[TBL] [Abstract][Full Text] [Related]
9. Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer.
Mitsui J; Fukuda Y; Azuma K; Tozaki H; Ishiura H; Takahashi Y; Goto J; Tsuji S
J Hum Genet; 2010 Jul; 55(7):448-55. PubMed ID: 20485446
[TBL] [Abstract][Full Text] [Related]
10. Exome versus transcriptome sequencing in identifying coding region variants.
Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815
[TBL] [Abstract][Full Text] [Related]
11. SNP discovery by transcriptome pyrosequencing.
Barbazuk WB; Schnable PS
Methods Mol Biol; 2011; 729():225-46. PubMed ID: 21365494
[TBL] [Abstract][Full Text] [Related]
12. Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome Analyzer.
Szelinger S; Kurdoglu A; Craig DW
Methods Mol Biol; 2011; 700():89-104. PubMed ID: 21204029
[TBL] [Abstract][Full Text] [Related]
13. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
Wagner MJ
Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
[TBL] [Abstract][Full Text] [Related]
14. Fast-forward genetics enabled by new sequencing technologies.
Schneeberger K; Weigel D
Trends Plant Sci; 2011 May; 16(5):282-8. PubMed ID: 21439889
[TBL] [Abstract][Full Text] [Related]
15. Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations.
Londin E; Yadav P; Surrey S; Kricka LJ; Fortina P
Methods Mol Biol; 2013; 1015():127-46. PubMed ID: 23824853
[TBL] [Abstract][Full Text] [Related]
16. Use of Ecotilling as an efficient SNP discovery tool to survey genetic variation in wild populations of Populus trichocarpa.
Gilchrist EJ; Haughn GW; Ying CC; Otto SP; Zhuang J; Cheung D; Hamberger B; Aboutorabi F; Kalynyak T; Johnson L; Bohlmann J; Ellis BE; Douglas CJ; Cronk QC
Mol Ecol; 2006 Apr; 15(5):1367-78. PubMed ID: 16626459
[TBL] [Abstract][Full Text] [Related]
17. Rapid gene identification in sugar beet using deep sequencing of DNA from phenotypic pools selected from breeding panels.
Ries D; Holtgräwe D; Viehöver P; Weisshaar B
BMC Genomics; 2016 Mar; 17():236. PubMed ID: 26980001
[TBL] [Abstract][Full Text] [Related]
18. Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
Ben-David E; Granot-Hershkovitz E; Monderer-Rothkoff G; Lerer E; Levi S; Yaari M; Ebstein RP; Yirmiya N; Shifman S
Hum Mol Genet; 2011 Sep; 20(18):3632-41. PubMed ID: 21680558
[TBL] [Abstract][Full Text] [Related]
19. Development of a next-generation sequencing method for BRCA mutation screening: a comparison between a high-throughput and a benchtop platform.
Chan M; Ji SM; Yeo ZX; Gan L; Yap E; Yap YS; Ng R; Tan PH; Ho GH; Ang P; Lee AS
J Mol Diagn; 2012 Nov; 14(6):602-12. PubMed ID: 22921312
[TBL] [Abstract][Full Text] [Related]
20. Targeted Sequencing Reveals Large-Scale Sequence Polymorphism in Maize Candidate Genes for Biomass Production and Composition.
Muraya MM; Schmutzer T; Ulpinnis C; Scholz U; Altmann T
PLoS One; 2015; 10(7):e0132120. PubMed ID: 26151830
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
