CONTENTS
Supplement 8
Volume 10
2009
BMC
Bioinformatics
Editor-in-Chief Melissa Norton, MD
Biology Editor Penny Webb, PhD
In-house Editor Tim Sands
BMC Bioinformatics
(www.biomedcentral.com/bmc bioinformatics) is an open access journal published by BioMed Central Ltd. The journal publishes original peer-reviewed research articles in all aspects of computational methods used in the analysis and annotation of sequences and structures, as well as all other areas of computational biology.
BMC Bioinformatics
(ISSN 1471-2105) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, Scopus, EMBASE, Thomson Reuters (ISI) and Google Scholar.
Contact BioMed Central supplements@ biomedcentral.com
Proceedings of the European Conference on Computational Biology
(ECCB) 2008 Workshop: Annotations, interpretation and management
of mutations (AIMM)
Cagliari, Italy
22 September 2008
Edited by Christopher JO Baker and Dietrich Rebholz-Schuhmann
www.biomedcentral.com/1471-2105/10?issue=S8
S1 Extraction of human kinase mutations from literature, databases and genotyping studies
Martin Krallinger, Jose MG Izarzugaza,
Carlos Rodriguez-Penagos and Alfonso Valencia S2 EnzyMiner: automatic identification of protein level mutations and thei impact on target enzymes from PubMed abstracts
Suveyda Yeniterzi and Ugur Sezerman
S3 Improved mutation tagging with gene identifiers applied to membrane protein stability prediction
Rainer Winnenburg, Conrad Plake and Michael Schroeder
S4 Annotation of protein residues based on a literature analysis: cross-validation against UniProtKb
Kevin Nagel,Antonio Jimeno-Yepes and Dietrich Rebholz-Schuhmann S5 An integrated approach to the interpretation of Single Amino Acid
Polymorphisms with the framework of CATH and Gene3D
Jose MG Izarzugaza,Anja Baresic, Lisa EM McMillan, Corin Yeats,Andrew B Clegg, Christine A Orengo, Andrew CR Martin and Alfonso Valencia
S6 From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways
Anna Bauer-Mehren, Laura I Furlong, Michael Rautschka and Ferran Sanz
S7 MtSNPscore: a combined evidence approach for assessing cumulative impact of
mitochondrial variations in disease
Anshu Bhardwaj, Mitali Mukerji, Shipra Sharma, Jinny Paul, Chaitanya S Gokhale,Achal K Srivastava and Shrish Tiwari
S8 Correlating protein function and stability through the analysis of single amino acid substitutions
Yana Bromberg and Burkhard Rost S9 Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations
Joke Reumers, Joost Schmkowitz and Fréderic Rousseau
S10 Pairwise and higher-order correlations among drug-resistance mutations in HIV-1 subtype protease
Omar Haq, Ronald M Levy,Alexandre V Morozov and Michael Andrec
