Mauno Vihinen

Orcid: 0000-0002-9614-7976

According to our database1, Mauno Vihinen authored at least 40 papers between 1988 and 2023.

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Bibliography

2023
VariBench, new variation benchmark categories and data sets.
Frontiers Bioinform., May, 2023

2020
Variation benchmark datasets: update, criteria, quality and applications.
Database J. Biol. Databases Curation, 2020

2019
How good are pathogenicity predictors in detecting benign variants?
PLoS Comput. Biol., 2019

2018
Representativeness of variation benchmark datasets.
BMC Bioinform., 2018

NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.
Database J. Biol. Databases Curation, 2018

2017
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Nucleic Acids Res., 2017

PON-SC - program for identifying steric clashes caused by amino acid substitutions.
BMC Bioinform., 2017

2016
PON-Sol: prediction of effects of amino acid substitutions on protein solubility.
Bioinform., 2016

2015
No more hidden solutions in bioinformatics.
Nat., 2015

Standard development at the Human Variome Project.
Database J. Biol. Databases Curation, 2015

2014
Identification of core T cell network based on immunome interactome.
BMC Syst. Biol., 2014

Variation ontology: annotator guide.
J. Biomed. Semant., 2014

2012
VarioML framework for comprehensive variation data representation and exchange.
BMC Bioinform., 2012

2010
Accuracy of protein hydropathy predictions.
Int. J. Data Min. Bioinform., 2010

2009
Evaluation of Accuracy and Applicability of Protein Models: Retrospective Analysis of Biological and Biomedical Predictions.
Silico Biol., 2009

2008
National research contributions: A case study on Finnish biomedical research.
Scientometrics, 2008

PseudoGeneQuest - Service for identification of different pseudogene types in the human genome.
BMC Bioinform., 2008

Model-based prediction of sequence alignment quality.
Bioinform., 2008

2007
Evaluation of Protein Hydropathy Scales.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2007

2006
A statistical score for assessing the quality of multiple sequence alignments.
BMC Bioinform., 2006

2005
Distribution of immunodeficiency fact files with XML - from Web to WAP.
BMC Medical Informatics Decis. Mak., 2005

On exact string matching of unique oligonucleotides.
Comput. Biol. Medicine, 2005

Dynamic covariation between gene expression and proteome characteristics.
BMC Bioinform., 2005

2004
Fast Iterative Gene Clustering Based on Information Theoretic Criteria for Selecting the Cluster Structure.
J. Comput. Biol., 2004

2003
On Postprocessing of Neural Network Prediction of Polyproline Type II Secondary Structures: Network Spectrum, Response Analysis, and Scattering.
Neural Comput. Appl., 2003

RankViaContact: ranking and visualization of amino acid contacts.
Bioinform., 2003

Efficient estimation of emission probabilities in profile hidden Markov models.
Bioinform., 2003

Signal transduction-related bioinformatics services.
Briefings Bioinform., 2003

2002
Mobile access to biological databases on the Internet.
IEEE Trans. Biomed. Eng., 2002

IDR: the ImmunoDeficiency Resource.
Nucleic Acids Res., 2002

2001
On preprocessing of protein sequences for neural network prediction of polyproline type II secondary structures.
Comput. Biol. Medicine, 2001

BioWAP, mobile Internet service for bioinformatics.
Bioinform., 2001

On Approximate String Matching of Unique Oligonucleotides.
Proceedings of the MEDINFO 2001, 2001

Binary Vector of Real Value Coding for Secondary Structure Prediction? A Case Study of Polyproline Type II Prediction.
Proceedings of the Medical Data Analysis, Second International Symposium, 2001

1999
KinMutBase, a database of human disease-causing protein kinase mutations.
Nucleic Acids Res., 1999

MUTbase: maintenance and analysis of distributed mutation databases.
Bioinform., 1999

1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Nucleic Acids Res., 1998

1996
BTKbase, mutation database for X-linked agammaglobulinemia (XLA).
Nucleic Acids Res., 1996

1992
MULTICOMP: a program package for multiple sequence comparison.
Comput. Appl. Biosci., 1992

1988
An algorithm for simultaneous comparison of several sequences.
Comput. Appl. Biosci., 1988


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