Related references
Note: Only part of the references are listed.Exploring functional variant discovery in non-coding regions with SInBaD
Kjong-Van Lehmann et al.
NUCLEIC ACIDS RESEARCH (2013)
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases
Miao-Xin Li et al.
NUCLEIC ACIDS RESEARCH (2012)
dbNSFP: A Lightweight Database of Human Nonsynonymous SNPs and Their Functional Predictions
Xiaoming Liu et al.
HUMAN MUTATION (2011)
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data
Gregory M. Cooper et al.
NATURE REVIEWS GENETICS (2011)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
MutationTaster evaluates disease-causing potential of sequence alterations
Jana Marie Schwarz et al.
NATURE METHODS (2010)
Single-nucleotide evolutionary constraint scores highlight disease-causing mutations
Gregory M. Cooper et al.
NATURE METHODS (2010)
The Universal Protein Resource (UniProt) in 2010
Rolf Apweiler et al.
NUCLEIC ACIDS RESEARCH (2010)
Identification of deleterious mutations within three human genomes
Sung Chun et al.
GENOME RESEARCH (2009)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Impact of residue accessible surface area on the prediction of protein secondary structures
Amir Momen-Roknabadi et al.
BMC BIOINFORMATICS (2008)
Sequence-based prioritization of nonsynonymous single-nucleotide polymorphisms for the study of disease mutations
Rui Jiang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
SNAP: predict effect of non-synonymous polymorphisms on function
Yana Bromberg et al.
NUCLEIC ACIDS RESEARCH (2007)
Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes
S. Nakken et al.
NEUROSCIENCE (2007)
PROFbval: predict flexible and rigid residues in proteins
A Schlessinger et al.
BIOINFORMATICS (2006)
Loss of protein structure stability as a major causative factor in monogenic disease
P Yue et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Combining prediction of secondary structure and solvent accessibility in proteins
R Adamczak et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)
Sequence-based prediction of pathological mutations
C Ferrer-Costa et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2004)
Human gene mutation database (HGMD®):: 2003 update
PD Stenson et al.
HUMAN MUTATION (2003)
Human non-synonymous SNPs: server and survey
V Ramensky et al.
NUCLEIC ACIDS RESEARCH (2002)
HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources
D Fredman et al.
NUCLEIC ACIDS RESEARCH (2002)
Predicting deleterious amino acid substitutions
PC Ng et al.
GENOME RESEARCH (2001)
Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation
D Chasman et al.
JOURNAL OF MOLECULAR BIOLOGY (2001)
Prediction of deleterious human alleles
S Sunyaev et al.
HUMAN MOLECULAR GENETICS (2001)
SNPs, protein structure, and disease
Z Wang et al.
HUMAN MUTATION (2001)
dbSNP: the NCBI database of genetic variation
ST Sherry et al.
NUCLEIC ACIDS RESEARCH (2001)
Share Paper
