Current status and new features of the Consensus Coding Sequence database - Wikidata - wikimedia - TriplyDB

Current status and new features of the Consensus Coding Sequence database

Current status and new features of the Consensus Coding Sequence database

http://www.wikidata.org/entity/Q24567717

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Perturbation of m6A writers reveals two distinct classes of mRNA methylation at internal and 5' sites Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research Decoding mechanisms by which silent codon changes influence protein biogenesis and function The neXtProt knowledgebase on human proteins: current status Lineage-Specific Changes in Biomarkers in Great Apes and Humans Explorations to improve the completeness of exome sequencing Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation The complexity, challenges and benefits of comparing two transporter classification systems in TCDB and Pfam Ensembl 2015 The 2014 Nucleic Acids Research Database Issue and an updated NAR online Molecular Biology Database Collection.Protein Bioinformatics Databases and Resources.Construction of a virtual Mycobacterium tuberculosis consensus genome and its application to data from a next generation sequencer.Genome annotation for clinical genomic diagnostics: strengths and weaknesses A Computational Methodology to Overcome the Challenges Associated With the Search for Specific Enzyme Targets to Develop Drugs Against Leishmania major.Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease.Genenames.org: the HGNC resources in 2015 Transcriptional diversity during lineage commitment of human blood progenitors.High throughput exome coverage of clinically relevant cardiac genes.Developmental regulation of human cortex transcription and its clinical relevance at single base resolution.Analysis of long non-coding RNAs highlights tissue-specific expression patterns and epigenetic profiles in normal and psoriatic skin.Systematic discovery of regulated and conserved alternative exons in the mammalian brain reveals NMD modulating chromatin regulators.Gene: a gene-centered information resource at NCBI.AnimalTFDB 2.0: a resource for expression, prediction and functional study of animal transcription factors.On the normalization of the minimum free energy of RNAs by sequence length.Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.Ratios of Four STAT3 Splice Variants in Human Eosinophils and Diffuse Large B Cell Lymphoma Cells Identification of genomic features in the classification of loss- and gain-of-function mutation.Restriction-based Multiple-fragment Assembly Strategy to Avoid Random Mutation during Long cDNA Cloning.Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth Hormone Mouse genome annotation by the RefSeq project RelA-Induced Interferon Response Negatively Regulates Proliferation deepBase v2.0: identification, expression, evolution and function of small RNAs, LncRNAs and circular RNAs from deep-sequencing data.A unified gene catalog for the laboratory mouse reference genome.Topology based identification and comprehensive classification of four-transmembrane helix containing proteins (4TMs) in the human genome Selective forces and mutational biases drive stop codon usage in the human genome: a comparison with sense codon usage Improving microRNA target prediction with gene expression profiles.Creating reference gene annotation for the mouse C57BL6/J genome assembly.Tissue-Specificity of Gene Expression Diverges Slowly between Orthologs, and Rapidly between Paralogs.

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P2860

Current status and new features of the Consensus Coding Sequence database

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description

2014 nî lūn-bûn

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2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունվարին հրատարակված գիտական հոդված

@hy

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

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2014年論文

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2014年論文

@zh-tw

2014年论文

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name

Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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type

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Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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prefLabel

Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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Current status and new features of the Consensus Coding Sequence database

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Nucleic Acids Research

P1476

Current status and new features of the Consensus Coding Sequence database

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P2093

Adam Frankish

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

Andrei Shkeda

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

Bhanu Rajput

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Catherine M Farrell

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Craig Wallin

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Daniel Barrell

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

David Haussler

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David Webb

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

Garth R Brown

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

James M Ostell

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P2860

Modernizing reference genome assemblies

A comparative analysis of exome capture

An integrated encyclopedia of DNA elements in the human genome

GENCODE: the reference human genome annotation for The ENCODE Project

Tracking and coordinating an international curation effort for the CCDS Project

Genome-wide annotation and quantitation of translation by ribosome profiling

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

The Genotype-Tissue Expression (GTEx) project

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D865-72

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scholarly article

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1240248

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10.1093/NAR/GKT1059

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P433

Database issue

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P478

42

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Stephen Trevanion

Laurens G Wilming

Jose M Gonzalez

Jane E Loveland

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2013-11-11T00:00:00Z

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258445480

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24217909

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3965069

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