Works matching IS 14712164 AND DT 2013 AND VI 14 AND IP Suppl 3

Results: 11

Multiscale modeling of the causal functional roles of nsSNPs in a genome-wide association study: pplication to hypoxia.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S9

By:

Li Xie;
Clara Ng;
Ali, Thahmina;
Valencia, Raoul;
Ferreira, Barbara L.;
Xue, Vincent;
Tanweer, Maliha;
Dan Zhou;
Haddad, Gabriel G.;
Bourne, Philip E.;
Lei Xie

Publication type:

Article

Revealing selection in cancer using the predicted unctional impact of cancer mutations. pplication to nomination of cancer drivers.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S8

By:

Reva, B.

Publication type:

Article

Assessment of computational methods for redicting the effects of missense mutations in uman cancers.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S7

By:

Gnad, Florian;
Baucom, Albion;
Mukhyala, Kiran;
Manning, Gerard;
Zhang, Zemin

Publication type:

Article

WS-SNPs&GO: a web server for predicting the eleterious effect of human protein variants sing functional annotation.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S6

By:

Capriotti, Emidio;
Calabrese, Remo;
Fariselli, Piero;
Martelli, Pier Luigi;
Altman, Russ B.;
Casadio, Rita

Publication type:

Article

A protein domain-centric approach for the omparative analysis of human and yeast henotypically relevant mutations.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S5

By:

Peterson, Thomas A.;
Park, DoHwan;
Kann, Maricel G.

Publication type:

Article

The SAAP pipeline and database: tools to analyze he impact and predict the pathogenicity of mutations.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S4

By:

Al-Numair, Nouf S.;
Martin, Andrew C. R.

Publication type:

Article

Identifying Mendelian disease genes with the Variant Effect Scoring Tool.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S3

By:

Carter, Hannah;
Douville, Christopher;
Stenson, Peter D.;
Cooper, David N.;
Karchin, Rachel

Publication type:

Article

Collective judgment predicts disease-associated ingle nucleotide variants.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S2

By:

Capriotti, Emidio;
Altman, Russ B.;
Bromberg, Yana

Publication type:

Article

Pathway analysis of genome-wide data improves arfarin dose prediction.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S11

By:

Daneshjou, Roxana;
Tatonetti, Nicholas P.;
Karczewski, Konrad J.;
Sagreiya, Hersh;
Bourgeois, Stephane;
Drozda, Katarzyna;
Burmester, James K.;
Tsunoda, Tatsuhiko;
Nakamura, Yusuke;
Kubo, Michiaki;
Tector, Matthew;
Limdi, Nita A.;
Cavallari, Larisa H.;
Perera, Minoli;
Johnson, Julie A.;
Klein, Teri E.;
Altman, Russ B.

Publication type:

Article

GWIS - model-free, fast and exhaustive search for istatic interactions in case-control GWAS.

Published in:

BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S10

By:

Goudey, Benjamin;
Rawlinson, David;
Qiao Wang;
Fan Shi;
Ferra, Herman;
Campbell, Richard M.;
Stern, Linda;
Inouye, Michael T.;
Ong, Cheng Soon;
Kowalczyk, Adam

Publication type:

Article

Thoughts from SNP-SIG 2012: future challenges in he annotation of genetic variations.

Published in:

2013

By:

Bromberg, Yana;
Capriotti, Emidio

Publication type:

Proceeding