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Domain Informations
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- Domain created: 2020-04-17T15:08:23Z
- Domain updated: 2023-08-19T19:59:02Z
- Domain expires: 2028-04-17T15:08:23Z 3 Years, 330 Days left
- Website age: 4 Years, 34 Days
- Registrar Domain ID: 33e3cb6103fd4a16b889757eb9a89fad-LROR
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Host Informations
| Host name | 193.62.193.83 |
| IP address | 193.62.193.83 |
| Location | Hinxton United Kingdom |
| Latitude | 52.055 |
| Longitude | 0.3132 |
| Timezone | Europe/London |
| Postal | CB10 |
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Site Inspections
Websites Listing
We found Websites Listing below when search with deciphergenomics.org on Search Engine
genome.ucsc.edu
Genome.ucsc.edu
Genome.ucsc.eduDA: 15 PA: 36 MOZ Rank: 51
DECIPHER CNVs Track Settings - University of California, …
For more information on DECIPHER, please contact contact@deciphergenomics. org. References. Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, Rajan D, Van Vooren S, …
Genome-euro.ucsc.eduDA: 20 PA: 18 MOZ Rank: 39
Deciphering Developmental Disorders (DDD) project
Accessing DDD data. The DDD study has a responsibility to all participants to maintain the confidentiality of their data and to maximise the opportunities for diagnosis. We are pioneering …
Ddduk.orgDA: 13 PA: 12 MOZ Rank: 27
Welcome to ClinGen - clinicalgenome.org
ClinGen was founded in 2013 by the National Human Genome Research Institute, ClinGen is a growing collaborative effort, involving three grants, seven principal investigators and over …
Clinicalgenome.orgDA: 22 PA: 22 MOZ Rank: 26
Citing Matchmaker Exchange - Matchmaker Exchange
Citing Matchmaker Exchange. Please acknowledge the Matchmaker Exchange, and the specific MME node that supported any discoveries, in publications. The table below provides …
Matchmakerexchange.orgDA: 26 PA: 12 MOZ Rank: 42
DECIPHER SNVs Track Settings
DECIPHER: Chromosomal Imbalance and Phenotype in Humans (SNVs) (All Phenotype and Literature tracks) Display mode:
Genome.ucsc.eduDA: 15 PA: 18 MOZ Rank: 38
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, …
A number sign (#) is used with this entry because Charcot-Marie-Tooth disease type 1A is caused by duplication of, or mutation in, the gene encoding peripheral myelin protein-22 (PMP22; …
Omim.orgDA: 12 PA: 13 MOZ Rank: 31
爬取DECIPHER Genomics数据库 - 生物信息文件夹
DECIPHER数据库收集了关于拷贝数变异的已知综合征及病例信息。本次爬取主要是收集里面每个基因的pLI、LOEUF、sHet、%HI等值，其他内容并不在目标中。通过网页 …
Pzweuj.github.ioDA: 16 PA: 33 MOZ Rank: 56
Mapping the Clinical Genome - Wellcome Sanger Institute
DECIPHER - Mapping the Clinical Genome. DECIPHER is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants. …
Sanger.ac.ukDA: 16 PA: 43 MOZ Rank: 67
DECIPHER: Supporting the interpretation and sharing of rare …
DECIPHER ( https://www.deciphergenomics.org) is a free web platform for sharing anonymized phenotype-linked variant data from rare disease patients. Its dynamic …
Onlinelibrary.wiley.comDA: 23 PA: 27 MOZ Rank: 59
マイクロアレイ染色体検査の結果解釈の補助ソフトウェアツール …
本ソフトウェアはマイクロアレイ染色体検査の結果において、①CNV syndromesとして登録されている症候群の欠失 (LossあるいはDeletion)と重複（GainあるいはDuplication） …
Cmg.med.keio.ac.jpDA: 18 PA: 18 MOZ Rank: 46
DECIPHER developer - EURAXESS
DECIPHER">https://www.deciphergenomics.org/">DECIPHER brings together genetic variation and clinical symptoms in patients with undiagnosed genetic disorders, to …
Euraxess.ec.europa.euDA: 21 PA: 12 MOZ Rank: 44
DECIPHER: Database of Chromosomal Imbalance and
Many patients suffering from developmental disorders harbor submicroscopic deletions or duplications that, by affecting the copy number of dosage-sensitive genes or …
Researchgate.netDA: 20 PA: 50 MOZ Rank: 38
New Honorary Professor - Academic Department of Medical …
The Department of Medical Genetics announces new Honorary Professor, Professor Helen Firth. “The rare award of a Honorary Professorship is testament to Professor Firth’s …
Medgen.medschl.cam.ac.ukDA: 24 PA: 29 MOZ Rank: 66
临床基因组分析相关数据库汇总 - 腾讯云开发者社区-腾讯云
ClinGen是美国国立卫生研究院(NIH)资助的数据库资源，用于精准医学，研究基因和变异的临床相关性。ClinGen提供了变异的剂量敏感性，有助于辨别突变的显隐性异常模式。
Cloud.tencent.comDA: 17 PA: 26 MOZ Rank: 57
January 2021 - Decipher-announce - public-lists.sanger.ac.uk
Upcoming domain change - https://deciphergenomics.org ===== Clinical genetics centres from around the world deposit data to DECIPHER. In view of this, the web domain will be updated …
Public-lists.sanger.ac.ukDA: 25 PA: 50 MOZ Rank: 95
Honorary Professor Helen Firth - Academic Department of Medical …
Professor Firth’s main research interests are in mapping of the clinical genome and the matching of rare genomic variants to empower discovery and diagnosis in rare disease. Helen chairs the …
Medgen.medschl.cam.ac.ukDA: 24 PA: 32 MOZ Rank: 72
Recommendations for whole genome sequencing in diagnostics …
EuroGentest is a European initiative, aiming to promoting accurate, reliable and high-quality genetic diagnostics across Europe. Initially funded by the European commission, …
Nature.comDA: 14 PA: 28 MOZ Rank: 59
Saturation genome editing of DDX3X clarifies pathogenicity of …
This study makes use of data generated by the DECIPHER community. A full list of centres who contributed to the generation of the data is available from …
Medrxiv.orgDA: 15 PA: 38 MOZ Rank: 71
怎样看懂一份基因检测报告:报告解读常用数据库
Leiden Open Variation Database (LOVD)是莱顿大学医学中心开发的开源式平台，其目的是提供一个灵活和免费的工具，收集和显示以基因为中心的DNA变异。. 基本信息包括基 …
Aisoutu.comDA: 15 PA: 10 MOZ Rank: 44
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