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Items: 5

1.

Accurate and comprehensive sequencing of personal genomes.

Ajay SS, Parker SC, Abaan HO, Fajardo KV, Margulies EH.

Genome Res. 2011 Sep;21(9):1498-505. doi: 10.1101/gr.123638.111.

2.

Toward better understanding of artifacts in variant calling from high-coverage samples.

Li H.

Bioinformatics. 2014 Oct 15;30(20):2843-51. doi: 10.1093/bioinformatics/btu356. Review.

3.

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. Review.

4.

Phylogenetic understanding of clonal populations in an era of whole genome sequencing.

Pearson T, Okinaka RT, Foster JT, Keim P.

Infect Genet Evol. 2009 Sep;9(5):1010-9. doi: 10.1016/j.meegid.2009.05.014. Review.

PMID:
19477301
5.

Annotating individual human genomes.

Torkamani A, Scott-Van Zeeland AA, Topol EJ, Schork NJ.

Genomics. 2011 Oct;98(4):233-41. doi: 10.1016/j.ygeno.2011.07.006. Review.

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