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Items: 9

1.

Characterization of missing human genome sequences and copy-number polymorphic insertions.

Kidd JM, Sampas N, Antonacci F, Graves T, Fulton R, Hayden HS, Alkan C, Malig M, Ventura M, Giannuzzi G, Kallicki J, Anderson P, Tsalenko A, Yamada NA, Tsang P, Kaul R, Wilson RK, Bruhn L, Eichler EE.

Nat Methods. 2010 May;7(5):365-71.

2.

Human genome variation in health and in neuropsychiatric disorders.

Buretić-Tomljanović A, Tomljanović D.

Psychiatr Danub. 2009 Dec;21(4):562-9. Review.

3.

Whole genome sequencing.

Ng PC, Kirkness EF.

Methods Mol Biol. 2010;628:215-26. doi: 10.1007/978-1-60327-367-1_12. Review.

PMID:
20238084
4.

Impacts of variation in the human genome on gene regulation.

Haraksingh RR, Snyder MP.

J Mol Biol. 2013 Nov 1;425(21):3970-7. doi: 10.1016/j.jmb.2013.07.015. Epub 2013 Jul 16. Review.

5.

One chromosome, one contig: complete microbial genomes from long-read sequencing and assembly.

Koren S, Phillippy AM.

Curr Opin Microbiol. 2015 Feb;23:110-20. doi: 10.1016/j.mib.2014.11.014. Epub 2014 Dec 1. Review.

6.

Challenges in studying genomic structural variant formation mechanisms: the short-read dilemma and beyond.

Onishi-Seebacher M, Korbel JO.

Bioessays. 2011 Nov;33(11):840-50. doi: 10.1002/bies.201100075. Epub 2011 Sep 30. Review.

PMID:
21959584
7.

A decade of structural variants: description, history and methods to detect structural variation.

Escaramís G, Docampo E, Rabionet R.

Brief Funct Genomics. 2015 Sep;14(5):305-14. doi: 10.1093/bfgp/elv014. Epub 2015 Apr 15. Review.

PMID:
25877305
8.

Human transposon tectonics.

Burns KH, Boeke JD.

Cell. 2012 May 11;149(4):740-52. doi: 10.1016/j.cell.2012.04.019. Review.

9.

Identification of structural variation in mouse genomes.

Keane TM, Wong K, Adams DJ, Flint J, Reymond A, Yalcin B.

Front Genet. 2014 Jul 2;5:192. doi: 10.3389/fgene.2014.00192. eCollection 2014. Review.

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