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Items: 6

1.

Predicting the functional effect of amino acid substitutions and indels.

Choi Y, Sims GE, Murphy S, Miller JR, Chan AP.

PLoS One. 2012;7(10):e46688. doi: 10.1371/journal.pone.0046688.

2.

The humankind genome: from genetic diversity to the origin of human diseases.

Beliz√°rio JE.

Genome. 2013 Dec;56(12):705-16. doi: 10.1139/gen-2013-0125. Review.

PMID:
24433206
3.

Rapid turnover of functional sequence in human and other genomes.

Ponting CP, Nellåker C, Meader S.

Annu Rev Genomics Hum Genet. 2011;12:275-99. doi: 10.1146/annurev-genom-090810-183115. Review.

PMID:
21721940
4.

Towards precision medicine: advances in computational approaches for the analysis of human variants.

Peterson TA, Doughty E, Kann MG.

J Mol Biol. 2013 Nov 1;425(21):4047-63. doi: 10.1016/j.jmb.2013.08.008. Review.

5.

Bioinformatic tools for identifying disease gene and SNP candidates.

Mooney SD, Krishnan VG, Evani US.

Methods Mol Biol. 2010;628:307-19. doi: 10.1007/978-1-60327-367-1_17. Review.

6.

Using bioinformatics to predict the functional impact of SNVs.

Cline MS, Karchin R.

Bioinformatics. 2011 Feb 15;27(4):441-8. doi: 10.1093/bioinformatics/btq695. Review.

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