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Studies of DECIPHER interactive web based database
National Center for Biotechnology Information
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
The DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the identification and interpretation of pathogenic genetic variation in patients with rare disorders.
Author: Eugene Bragin…
Published: 2014/01/01
Publication: Nucleic A…
National Center for Biotechnology Information
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
Many patients suffering from developmental disorders harbor submicroscopic deletions or duplications that, by affecting the copy number of dosage-sensitive genes or disrupting normal gene expression, lead to disease. However, many aberrations are novel
Author: Helen V. Firth, …
Published: 2009/04/04
Publication: Am J Hu…
PubMed
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
The DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the identification and interpretation of pathogenic genetic variation in patients with rare disorders.
Author: Eugene Bragin
Published: 2014/1
Keywords: National In…
PubMed
DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders
Patients with developmental disorders often harbour sub-microscopic deletions or duplications that lead to a disruption of normal gene expression or perturbation in the copy number of dosage-sensitive genes. Clinical interpretation for such patients in
Author: Ganesh J Swa…
Published: 2012/10/15
Keywords: National In…
ResearchGate
DECIPHER: Database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
The DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the identification and interpretation of pathogenic genetic variation in patients with rare disorders.
Published: 2013/10/22
DOI: 10.1093/nar/gkt937
PubMed
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
Many patients suffering from developmental disorders harbor submicroscopic deletions or duplications that, by affecting the copy number of dosage-sensitive genes or disrupting normal gene expression, lead to disease. However, many aberrations are novel
Author: Helen V Firth
Published: 2009/4
Keywords: National In…
National Center for Biotechnology Information
Diagnostic Interpretation of Array Data Using Public Databases and Internet Sources
The range of commercially available array platforms and analysis software packages is expanding and their utility is improving, making reliable detection of copy-number variants (CNVs) relatively straightforward. Reliable interpretation of CNV data, however,
Author: Nicole de Leeu…
Published: 2012/06
DOI: 10.1002/humu.22…
ResearchGate
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources
Many patients suffering from developmental disorders harbor submicroscopic deletions or duplications that, by affecting the copy number of dosage-sensitive genes or disrupting normal gene expression, lead to disease. However, many aberrations are novel
Published: 2009/05/01
DOI: 10.1016/j.ajhg.200…
DECIPHER
https://www.deciphergenomics.org
DECIPHER v11.25: Mapping the clinical genome
WebExplore DECIPHER. It's free and you don't need to log in. DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER …
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  Genes with Sequence Variants in DECIPHER This is a list of genes for …
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Wellcome Sanger Institute
https://www.sanger.ac.uk/tool/decipher-mapping-the-clinical-genome
DECIPHER – Mapping the Clinical Genome - Wellcome Sanger …
WebDECIPHER is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants. DECIPHER enhances clinical …
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DECIPHER Tutorial
deciphergenomics.org
(PDF) DECIPHER: Database for the interpretation of ... - …
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Wikipedia
https://en.wikipedia.org/wiki/DECIPHER
DECIPHER - Wikipedia
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DECIPHER is a web-based resource and database of genomic variation data from analysis of patient DNA. It documents submicroscopic chromosome abnormalities (microdeletions and duplications) and pathogenic sequence variants (single nucleotide variants - SNVs, Insertions, Deletions, InDels), from over 25000 patients and maps them to the human genome using Ensembl or UCSC Genome Browser
Wikipedia · Text under CC-BY-SA license
- Estimated Reading Time: 9 mins
Wellcome Sanger Institute
https://www.sanger.ac.uk/group/decipher
DECIPHER - Wellcome Sanger Institute
WebThe DECIPHER database and team moved to EMBL’s European Bioinformatics Institute (EMBL-EBI) in July 2023. The database can be accessed at: …
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Decipher Database
Decipher Definition Biology
Decipher Genes
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Decipher Uk
Decipher Biosciences
National Center for Biotechnology Information
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667985
DECIPHER: Database of Chromosomal Imbalance and …
WebApr 4, 2009 · To facilitate the analysis of these rare events, we have developed an interactive web-based database called DECIPHER (Database of Chromosomal …
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Decipher Database
Decipher Genetics
Decipher Genome Browser
+2
Decipher Survey
Publish Year:2009
illumina.github.io
https://illumina.github.io/.../data-sources/decipher
DECIPHER | Nirvana
WebOverview. DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources) is an interactive web-based database which incorporates a suite …
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Decipher Database
Clinical Interpretation
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What is DECIPHER database?DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources) is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants.
DECIPHER - Wellcome Sanger Institute
sanger.ac.uk
What is decipher & how does it work?DECIPHER is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants. DECIPHER enhances clinical diagnosis by retrieving information from a variety of bioinformatics resources relevant to the variant found in the patient.
DECIPHER – Mapping the Clinical Genome - Wellcome Sanger Institute
sanger.ac.uk
What EMBL-EBI data is used for the decipher project?The DECIPHER project has always benefited from EMBL-EBI data, displaying information from many of the institute’s data resources to assist in variant interpretation. These include data from Ensembl, the Ensembl Variant Effect Predictor (VEP), UniProt, Protein Data Bank in Europe (PDBe), and Gene2Phenotype.
DECIPHER database for rare diseases joins EMBL-EBI
embl.org
Who contributes to the DECIPHER database?Contributing to the DECIPHER database is a Consortium, comprising an international network of academic departments of clinical genetics now numbering more than 100 centers and having uploaded more than 2000 cases (current statistics can be found on the DECIPHER homepage).
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Hu…
ncbi.nlm.nih.gov
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National Center for Biotechnology Information
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965078
DECIPHER: database for the interpretation of phenotype-linked …
WebJan 1, 2014 · The DECIPHER database ( https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the …
Tags:
Decipher Database
Genetic Variation
Publish Year:2014
+2
10.1093/nar/gkt937
Published:2014/01/01
Oxford Academic
https://academic.oup.com/hmg/article/21/R1/R37/658334
DECIPHER: web-based, community resource for clinical …
WebSep 8, 2012 · DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders. Ganesh J. Swaminathan. , Eugene Bragin. , Eleni …
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Clinical Interpretation
Decipher Pathology
Publish Year:2012
Wiley Online Library
https://onlinelibrary.wiley.com/doi/full/10.1002/humu.24340
DECIPHER: Supporting the interpretation and ... - Wiley Online …
WebDECIPHER ( https://www.deciphergenomics.org) is a free web platform for sharing anonymized phenotype-linked variant data from rare disease patients. Its dynamic …
DECIPHER
https://www.deciphergenomics.org/files/pdfs/...
[PDF]
Searching DECIPHER
WebDECIPHER has an advanced search facility that allows querying the database using a combination of terms including phenotypes, gene symbols, chromosomal …
PubMed
https://pubmed.ncbi.nlm.nih.gov/24150940
DECIPHER: database for the interpretation of phenotype-linked …
WebThe DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the identification and …
Tags:
Decipher Database
Genetic Variation
Publish Year:2014
European Molecular Biology Laboratory
https://www.embl.org/news/science/decipher...
DECIPHER database for rare diseases joins EMBL-EBI
WebJul 6, 2023 · The DECIPHER website and database, which are used globally by researchers and clinicians to interpret and share phenotypic and genotypic data from …
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Decipher Database
Decipher Rare Disease
PubMed
https://pubmed.ncbi.nlm.nih.gov/22962312
DECIPHER: web-based, community resource for clinical
WebOct 15, 2012 · The DECIPHER project (https://decipher.sanger.ac.uk) was established in 2004 as an accessible online repository of genomic and associated phenotypic data with …
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Clinical Interpretation
Decipher Rare Disease
Decipher Pathology
Limbus News
https://blog.limbus-medtec.com/decipher-in-cnv...
DECIPHER in CNV analysis. The Database of Chromosomal …
WebApr 8, 2022. What is DECIPHER? The Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources (DECIPHER) is an interactive web …
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Decipher Database
Decipher Cnv
Wellcome Sanger Institute
https://www.sanger.ac.uk/science/tools
Tools - Wellcome Sanger Institute
WebDECIPHER is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants. DECIPHER ... Analysis
Academia.edu
https://www.academia.edu/10454994/DECIPHER...
(PDF) DECIPHER: database for the interpretation of phenotype …
WebOct 22, 2013 · DECIPHER (https://decipher.sanger.ac.uk) is a web-based platform for secure deposition, analysis, and sharing of plausibly pathogenic genomic variants from …
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Decipher Database
Eleni Chatzimichali
ResearchGate
https://www.researchgate.net/publication/258037025
(PDF) DECIPHER: Database for the interpretation of
WebOct 22, 2013 · The DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the …
Tags:
Decipher Database
Genetic Variation
PubMed
https://pubmed.ncbi.nlm.nih.gov/19344873
DECIPHER: Database of Chromosomal Imbalance and …
WebTo facilitate the analysis of these rare events, we have developed an interactive web-based database called DECIPHER (Database of Chromosomal Imbalance and …
National Center for Biotechnology Information
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027376
Diagnostic Interpretation of Array Data Using Public Databases …
WebThe DECIPHER is an interactive Web-based database that incorporates a suite of tools designed to aid the interpretation of submicroscopic chromosomal imbalances.
Tags:
Decipher Database
Publish Year:2012
Interpret Data Research
+2
10.1002/humu.22049
Published:2012/06
ResearchGate
https://www.researchgate.net/publication/24256247
DECIPHER: Database of Chromosomal Imbalance and
WebMay 1, 2009 · To facilitate the analysis of these rare events, we have developed an interactive web-based database called DECIPHER (Database of Chromosomal …
researchgate.net
https://www.researchgate.net/publication/230827021
(PDF) DECIPHER: Web-based, community resource for clinical ...
WebSep 8, 2012 · DECIPHER: Web-based, community resource for clinical interpretation of rare variants in developmental disorders. September 2012. Human Molecular Genetics 21 (R1):R37-44. DOI:...
Oxford Academic
https://academic.oup.com/nar/article/42/D1/D993/1068216
DECIPHER: database for the interpretation of phenotype-linked …
WebOct 21, 2013 · The DECIPHER database ( https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the …
Tags:
Decipher Database
Genetic Variation
Publish Year:2014
Decipher Cnv
cardiodb.org
https://www.cardiodb.org
Cardiovascular Genetics and Genomics
WebDECIPHER. DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources) is an interactive web-based database which incorporates a suite …
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Decipher Database
Genomics
National Genomics Data Center
https://ngdc.cncb.ac.cn/databasecommons/database/id/284
DECIPHER - Database Commons - National Genomics Data Center
WebDECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders. [PMID: 22962312] Swaminathan GJ, Bragin E, Chatzimichali …
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Decipher Database
Clinical Interpretation
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