about
Data integration workflow for search of disease driving genes and genetic variantsSnpdat: Easy and rapid annotation of results from de novo snp discovery projects for model and non-model organismsConcept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions.Next generation tools for the annotation of human SNPsANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataMeet me halfway: when genomics meets structural bioinformatics.Genome-wide survey of allele-specific splicing in humans.The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.Functional analysis of novel SNPs and mutations in human and mouse genomes.Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databasesScripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver.A proteogenomic analysis of Anopheles gambiae using high-resolution Fourier transform mass spectrometry.Natural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution.SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.DNA copy number aberrations in breast cancer by array comparative genomic hybridization.A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity.AnnotQTL: a new tool to gather functional and comparative information on a genomic region.Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.Distinguishing the disease-associated SNPs based on composition frequency analysis.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Snap: an integrated SNP annotation platform.
@ast
Snap: an integrated SNP annotation platform.
@en
type
label
Snap: an integrated SNP annotation platform.
@ast
Snap: an integrated SNP annotation platform.
@en
prefLabel
Snap: an integrated SNP annotation platform.
@ast
Snap: an integrated SNP annotation platform.
@en
P2093
P2860
P50
P356
P1476
Snap: an integrated SNP annotation platform.
@en
P2093
P2860
P304
P356
10.1093/NAR/GKL969
P407
P433
Database issue
P577
2006-11-29T00:00:00Z