Distribution and intensity of constraint in mammalian genomic sequence
about
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectA user's guide to the encyclopedia of DNA elements (ENCODE)Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysisIntegrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locusPhased whole-genome genetic risk in a family quartet using a major allele reference sequenceUsing comparative genomics to reorder the human genome sequence into a virtual sheep genomeA catalog of neutral and deleterious polymorphism in yeastThe case for junk DNAWhat fraction of the human genome is functional?Five-vertebrate ChIP-seq reveals the evolutionary dynamics of transcription factor bindingEnsembl 2008Variation in genome-wide mutation rates within and between human familiesAn integrated encyclopedia of DNA elements in the human genomeGenomic views of distant-acting enhancersDiamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28EXTREME: an online EM algorithm for motif discoveryEnsembl 2014Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesisEnsembl 2011Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndromeMutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenanceUltraconservation identifies a small subset of extremely constrained developmental enhancersVectorBase: a data resource for invertebrate vector genomicsStrong purifying selection at synonymous sites in D. melanogasterMutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated NeuronsPhenotype-driven strategies for exome prioritization of human Mendelian disease genes.Methods to detect selection on noncoding DNAComputational and statistical approaches to analyzing variants identified by exome sequencingLa FAM fatale: USP9X in development and diseaseRecessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor developmentExpression variants of the lipogenic AGPAT6 gene affect diverse milk composition phenotypes in Bos taurusUnderstanding rare and common diseases in the context of human evolutionThe genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevanceConnecting the CNTNAP2 Networks with Neurodevelopmental DisordersMutations in DCHS1 cause mitral valve prolapseEnsembl 2012Lagging-strand replication shapes the mutational landscape of the genomeNEK1 variants confer susceptibility to amyotrophic lateral sclerosisEnredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogsMapping Argonaute and conventional RNA-binding protein interactions with RNA at single-nucleotide resolution using HITS-CLIP and CIMS analysis
P2860
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P2860
Distribution and intensity of constraint in mammalian genomic sequence
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Distribution and intensity of constraint in mammalian genomic sequence
@ast
Distribution and intensity of constraint in mammalian genomic sequence
@en
type
label
Distribution and intensity of constraint in mammalian genomic sequence
@ast
Distribution and intensity of constraint in mammalian genomic sequence
@en
prefLabel
Distribution and intensity of constraint in mammalian genomic sequence
@ast
Distribution and intensity of constraint in mammalian genomic sequence
@en
P2093
P2860
P3181
P356
P1433
P1476
Distribution and intensity of constraint in mammalian genomic sequence
@en
P2093
P2860
P304
P3181
P356
10.1101/GR.3577405
P407
P577
2005-07-01T00:00:00Z