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Items: 1 to 20 of 84

1.

A map of human genome variation from population-scale sequencing.

1000 Genomes Project Consortium., Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA.

Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534. Erratum in: Nature. 2011 May 26;473(7348):544. Xue, Yali [added]; Cartwright, Reed A [added]; Altshuler, David L [corrected to Altshuler, David]; Kebbel, Andrew [corrected to Keebler, Jonathan]; Koko-Gonzales, Paula [corrected to Kokko-Gonzales, Paula]; Nickerson, Debbie A [corrected to Nickerson, Deborah A].

2.
3.

Molecular genetic studies of complex phenotypes.

Marian AJ.

Transl Res. 2012 Feb;159(2):64-79. doi: 10.1016/j.trsl.2011.08.001. Epub 2011 Aug 31. Review.

4.

Genetic variation in the acorn barnacle from allozymes to population genomics.

Flight PA, Rand DM.

Integr Comp Biol. 2012 Sep;52(3):418-29. doi: 10.1093/icb/ics099. Epub 2012 Jul 4. Review.

5.

Genomic resources and their influence on the detection of the signal of positive selection in genome scans.

Manel S, Perrier C, Pratlong M, Abi-Rached L, Paganini J, Pontarotti P, Aurelle D.

Mol Ecol. 2016 Jan;25(1):170-84. doi: 10.1111/mec.13468. Epub 2015 Dec 17. Review.

PMID:
26562485
6.

Understanding genetic variation and function- the applications of next generation sequencing.

Harrison RJ.

Semin Cell Dev Biol. 2012 Apr;23(2):230-6. doi: 10.1016/j.semcdb.2012.01.006. Epub 2012 Jan 20. Review.

PMID:
22285423
7.

SNP and haplotype variation in the human genome.

Salisbury BA, Pungliya M, Choi JY, Jiang R, Sun XJ, Stephens JC.

Mutat Res. 2003 May 15;526(1-2):53-61. Review.

PMID:
12714183
8.

Genomic sequencing in cancer.

Tuna M, Amos CI.

Cancer Lett. 2013 Nov 1;340(2):161-70. doi: 10.1016/j.canlet.2012.11.004. Epub 2012 Nov 23. Review.

9.

Computational methods for discovering structural variation with next-generation sequencing.

Medvedev P, Stanciu M, Brudno M.

Nat Methods. 2009 Nov;6(11 Suppl):S13-20. doi: 10.1038/nmeth.1374. Review.

PMID:
19844226
10.

Genome Wide Sampling Sequencing for SNP Genotyping: Methods, Challenges and Future Development.

Jiang Z, Wang H, Michal JJ, Zhou X, Liu B, Woods LC, Fuchs RA.

Int J Biol Sci. 2016 Jan 1;12(1):100-8. doi: 10.7150/ijbs.13498. eCollection 2016 Jan 1. Review.

11.

Genetic variation and the de novo assembly of human genomes.

Chaisson MJ, Wilson RK, Eichler EE.

Nat Rev Genet. 2015 Nov;16(11):627-40. doi: 10.1038/nrg3933. Epub 2015 Oct 7. Review.

12.

Advances in understanding cancer genomes through second-generation sequencing.

Meyerson M, Gabriel S, Getz G.

Nat Rev Genet. 2010 Oct;11(10):685-96. doi: 10.1038/nrg2841. Review.

PMID:
20847746
13.

Research progress of plant population genomics based on high-throughput sequencing.

Yunsheng W.

Yi Chuan. 2016 Aug;38(8):688-99. doi: 10.16288/j.yczz.16-061. Review.

PMID:
27531607
14.

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data.

Cooper GM, Shendure J.

Nat Rev Genet. 2011 Aug 18;12(9):628-40. doi: 10.1038/nrg3046. Review.

PMID:
21850043
15.

Genome-wide scans for loci under selection in humans.

Ronald J, Akey JM.

Hum Genomics. 2005 Jun;2(2):113-25. Review.

16.

Small insertions and deletions (INDELs) in human genomes.

Mullaney JM, Mills RE, Pittard WS, Devine SE.

Hum Mol Genet. 2010 Oct 15;19(R2):R131-6. doi: 10.1093/hmg/ddq400. Epub 2010 Sep 21. Review.

17.

Direct mutation analysis by high-throughput sequencing: from germline to low-abundant, somatic variants.

Gundry M, Vijg J.

Mutat Res. 2012 Jan 3;729(1-2):1-15. doi: 10.1016/mrfmmm.2011.10.001. Epub 2011 Oct 12. Review.

18.

Cancer genome sequencing: understanding malignancy as a disease of the genome, its conformation, and its evolution.

Patel LR, Nykter M, Chen K, Zhang W.

Cancer Lett. 2013 Nov 1;340(2):152-60. doi: 10.1016/j.canlet.2012.10.018. Epub 2012 Oct 27. Review.

19.

Targeted deep resequencing of the human cancer genome using next-generation technologies.

Myllykangas S, Ji HP.

Biotechnol Genet Eng Rev. 2010;27:135-58. Review.

20.

Computational methods and resources for the interpretation of genomic variants in cancer.

Tian R, Basu MK, Capriotti E.

BMC Genomics. 2015;16 Suppl 8:S7. doi: 10.1186/1471-2164-16-S8-S7. Epub 2015 Jun 18. Review.

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