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