VariBench: A Benchmark Database for Variations
暂无分享,去创建一个
[1] Peter H. Baenziger,et al. In silico functional profiling of human disease‐associated and polymorphic amino acid substitutions , 2010, Human mutation.
[2] Lode Wyns,et al. SABmark- a benchmark for sequence alignment that covers the entire known fold space , 2005, Bioinform..
[3] Rachel Kolodny,et al. Comprehensive evaluation of protein structure alignment methods: scoring by geometric measures. , 2005, Journal of molecular biology.
[4] Olivier Poch,et al. BAliBASE: a benchmark alignment database for the evaluation of multiple alignment programs , 1999, Bioinform..
[5] András Kocsor,et al. A Protein Classification Benchmark collection for machine learning , 2007, Nucleic Acids Res..
[6] M. Vihinen,et al. Performance of mutation pathogenicity prediction methods on missense variants , 2011, Human mutation.
[7] G. Schreiber,et al. Assessing computational methods for predicting protein stability upon mutation: good on average but not in the details. , 2009, Protein engineering, design & selection : PEDS.
[8] John K. Lyon,et al. What is a database , 1973, SGMD.
[9] John P. Overington,et al. HOMSTRAD: A database of protein structure alignments for homologous families , 1998, Protein science : a publication of the Protein Society.
[10] George P Patrinos,et al. Locus‐specific database domain and data content analysis: evolution and content maturation toward clinical use a , 2010, Human mutation.
[11] L. Serrano,et al. Predicting changes in the stability of proteins and protein complexes: a study of more than 1000 mutations. , 2002, Journal of molecular biology.
[12] M. Vihinen. How to evaluate performance of prediction methods? Measures and their interpretation in variation effect analysis , 2012, BMC Genomics.
[13] Christophe Béroud,et al. Bioinformatics identification of splice site signals and prediction of mutation effects , 2010 .
[14] Michele Magrane,et al. UniProt Knowledgebase: a hub of integrated protein data , 2011, Database J. Biol. Databases Curation.
[15] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..
[16] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[17] Robert C. Edgar,et al. MUSCLE: multiple sequence alignment with high accuracy and high throughput. , 2004, Nucleic acids research.
[18] M. Vihinen,et al. Immunodeficiency mutation databases (IDbases). , 1998, Human mutation.
[19] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[20] Tatiana A. Tatusova,et al. NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy , 2011, Nucleic Acids Res..
[21] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[22] Life Technologies,et al. A map of human genome variation from population-scale sequencing , 2011 .
[23] K. Sirotkin,et al. The NCBI dbGaP database of genotypes and phenotypes , 2007, Nature Genetics.
[24] Syed Haider,et al. Ensembl BioMarts: a hub for data retrieval across taxonomic space , 2011, Database J. Biol. Databases Curation.
[25] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[26] Debasis Dash,et al. HGVbaseG2P: a central genetic association database , 2008, Nucleic Acids Res..
[27] David C. Jones,et al. CATH--a hierarchic classification of protein domain structures. , 1997, Structure.
[28] Alexander V. Diemand,et al. The Swiss‐Prot variant page and the ModSNP database: A resource for sequence and structure information on human protein variants , 2004, Human mutation.
[29] Harri Lähdesmäki,et al. Systematic Analysis of Disease-Related Regulatory Mutation Classes Reveals Distinct Effects on Transcription Factor Binding , 2009, Silico Biol..
[30] John L Hopper,et al. Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics , 2009, Human mutation.
[31] G. Church,et al. Preferred analysis methods for Affymetrix GeneChips revealed by a wholly defined control dataset , 2005, Genome Biology.
[32] Christus,et al. A General Method Applicable to the Search for Similarities in the Amino Acid Sequence of Two Proteins , 2022 .
[33] Ourania Horaitis,et al. A database of locus-specific databases , 2007, Nature Genetics.
[34] Sue Povey,et al. The Human Variome Project , 2008, Science.
[35] Mauno Vihinen,et al. Performance of protein stability predictors , 2010, Human mutation.
[36] R. E. Tully,et al. Locus Reference Genomic sequences: an improved basis for describing human DNA variants , 2010, Genome Medicine.
[37] Carol A. Bocchini,et al. A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®) , 2011, Human mutation.
[38] J. Thompson,et al. Issues in bioinformatics benchmarking: the case study of multiple sequence alignment , 2010, Nucleic acids research.
[39] M. Vihinen,et al. Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods , 2009, Human mutation.
[40] M. A. McClure,et al. Comparative analysis of multiple protein-sequence alignment methods. , 1994, Molecular biology and evolution.
[41] P. Stenson,et al. The Human Gene Mutation Database: 2008 update , 2009, Genome Medicine.
[42] Akinori Sarai,et al. ProTherm and ProNIT: thermodynamic databases for proteins and protein–nucleic acid interactions , 2005, Nucleic Acids Res..
[43] M. Daly,et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.
[44] Ying Gao,et al. Bioinformatics Applications Note Sequence Analysis Cd-hit Suite: a Web Server for Clustering and Comparing Biological Sequences , 2022 .
[45] G. Rubin,et al. A computer program for aligning a cDNA sequence with a genomic DNA sequence. , 1998, Genome research.
[46] M. Vihinen,et al. Classification of mismatch repair gene missense variants with PON‐MMR , 2012, Human mutation.
[47] Zhiping Weng,et al. Protein–protein docking benchmark version 4.0 , 2010, Proteins.
[48] Mauno Vihinen,et al. PON‐P: Integrated predictor for pathogenicity of missense variants , 2012, Human mutation.
[49] Gajendra P. S. Raghava,et al. OXBench: A benchmark for evaluation of protein multiple sequence alignment accuracy , 2003, BMC Bioinformatics.
[50] Rachel Karchin,et al. Next generation tools for the annotation of human SNPs , 2009, Briefings Bioinform..
[51] Peter B. McGarvey,et al. A comprehensive protein-centric ID mapping service for molecular data integration , 2011, Bioinform..
[52] Qianqian Zhu,et al. Preferred analysis methods for Affymetrix GeneChips. II. An expanded, balanced, wholly-defined spike-in dataset , 2010, BMC Bioinformatics.
[53] Terence P. Speed,et al. A benchmark for Affymetrix GeneChip expression measures , 2004, Bioinform..
[54] Marek Kimmel,et al. Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed , 2011, Human mutation.
[55] Tim J. P. Hubbard,et al. SCOP: a structural classification of proteins database , 1998, Nucleic Acids Res..
[56] Piero Fariselli,et al. A neural-network-based method for predicting protein stability changes upon single point mutations , 2004, ISMB/ECCB.
[57] Emidio Capriotti,et al. Bioinformatics for personal genome interpretation , 2012, Briefings Bioinform..