Allelic expression of deleterious protein-coding variants across human tissues. - Wikidata - wikimedia - TriplyDB

Allelic expression of deleterious protein-coding variants across human tissues.

Allelic expression of deleterious protein-coding variants across human tissues.

http://www.wikidata.org/entity/Q35160833

about

SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data.Assessing allele-specific expression across multiple tissues from RNA-seq read data Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels Non-Coding Loss-of-Function Variation in Human Genomes.Analysis of stop-gain and frameshift variants in human innate immunity genes.Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations QuASAR: quantitative allele-specific analysis of reads.Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease Personalized biochemistry and biophysics.Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.Tools and best practices for data processing in allelic expression analysis.Adult porcine genome-wide DNA methylation patterns support pigs as a biomedical model.GeneiASE: Detection of condition-dependent and static allele-specific expression from RNA-seq data without haplotype information.Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome A haplotype-based normalization technique for the analysis and detection of allele specific expression.High-throughput allele-specific expression across 250 environmental conditions.Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population.Analysis of population-specific pharmacogenomic variants using next-generation sequencing data.Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change.Epigenetic supersimilarity of monozygotic twin pairs.Pharmacogenomics of GPCR Drug Targets.ASElux: An Ultra-Fast and Accurate Allelic Reads Counter.Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease.Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes.

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Allelic expression of deleterious protein-coding variants across human tissues.

http://www.wikidata.org/entity/Q35160833

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Allelic expression of deleterious protein-coding variants across human tissues.

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Allelic expression of deleterious protein-coding variants across human tissues.

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type

label

Allelic expression of deleterious protein-coding variants across human tissues.

@ast

Allelic expression of deleterious protein-coding variants across human tissues.

@en

prefLabel

Allelic expression of deleterious protein-coding variants across human tissues.

@ast

Allelic expression of deleterious protein-coding variants across human tissues.

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JOURNAL.PGEN.1004304

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Allelic expression of deleterious protein-coding variants across human tissues.

@en

P2093

Daniel G Macarthur

http://www.w3.org/2001/XMLSchema#string

David A Knowles

http://www.w3.org/2001/XMLSchema#string

Jin Billy Li

http://www.w3.org/2001/XMLSchema#string

Kevin S Smith

http://www.w3.org/2001/XMLSchema#string

Kimberly R Kukurba

http://www.w3.org/2001/XMLSchema#string

Meng How Tan

http://www.w3.org/2001/XMLSchema#string

Michael Snyder

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Monkol Lek

http://www.w3.org/2001/XMLSchema#string

Robert Piskol

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Xin Li

http://www.w3.org/2001/XMLSchema#string

P2860

dbSNP: the NCBI database of genetic variation

A map of human genome variation from population-scale sequencing

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

Fast and accurate short read alignment with Burrows-Wheeler transform

TopHat: discovering splice junctions with RNA-Seq

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

A method and server for predicting damaging missense mutations

The Sequence Alignment/Map format and SAMtools

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome

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e1004304

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scholarly article

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10.1371/JOURNAL.PGEN.1004304

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5

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10

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Stephen Montgomery

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2014-05-01T00:00:00Z

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262018045

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