Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 11:34, 21 Nov 2018 (not approved):
'domains' has been modified:
Before:
Biomedical Science
Chromosomal aberration
Chromosome
Genome visualisation
Life Science
Variant
After:
Biomedical Science
Chromosomal aberration
Chromosome
Genome visualisation
Life Science
Sequence variant
Added:
Sequence variant
Removed:
Variant
'miriam_id' has been modified:
Before:
After: None
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 17:19, 17 Oct 2018 (approved):
'organizations' has been modified:
Before:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
Cambridge South REC, UK|https://www.hra.nhs.uk/about-us/committees-and-services/res-and-recs/search-research-ethics-committees/|Funds
After:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
Cambridge South REC, UK|https://www.hra.nhs.uk/about-us/committees-and-services/res-and-recs/search-research-ethics-committees/|Funds
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK|http://www.sanger.ac.uk|Maintains
Added:
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK|http://www.sanger.ac.uk|Maintains
Removed:
'description' has been modified:
Before: DECIPHER (Database of Chromosomal Imbalance 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 submicroscopic chromosomal imbalance, inversions, and translocations.
After: DECIPHER (Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources) is an interactive web-based resource that incorporates a suite of tools designed to aid the interpretation of submicroscopic chromosomal imbalance, inversions, and translocations.
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 20:54, 09 Aug 2018 (approved):
'licences' has been modified:
Before:
Data sharing|https://decipher.sanger.ac.uk/datasharing|Data
After:
DECIPHER Data Sharing|https://decipher.sanger.ac.uk/datasharing|Data
Added:
DECIPHER Data Sharing|https://decipher.sanger.ac.uk/datasharing|Data
Removed:
Data sharing|https://decipher.sanger.ac.uk/datasharing|Data
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'JForeman' at 09:32, 09 Aug 2018 (approved):
'contactEmail' has been modified:
Before: ganesh.swaminathan@sanger.ac.uk
After: jf11@sanger.ac.uk
'contact' has been modified:
Before: G. Jawahar Swaminathan
After: Julia Foreman
'contactORCID' has been modified:
Before: https://orcid.org/0000-0002-0215-4084
After:
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 16:38, 03 Aug 2018 (approved):
'licences' has been modified:
Before:
After:
Data sharing|https://decipher.sanger.ac.uk/datasharing|Data
Added:
Data sharing|https://decipher.sanger.ac.uk/datasharing|Data
Removed:
'supportLinks' has been modified:
Before:
After:
blog|https://decipher.sanger.ac.uk/
contact form|https://decipher.sanger.ac.uk/
email|decipher@sanger.ac.uk
online documentation|https://decipher.sanger.ac.uk/files/pdfs/decipher_database_flowchart.pdf
online documentation|https://decipher.sanger.ac.uk/files/pdfs/decipher_ethical_framework.pdf
Added:
blog|https://decipher.sanger.ac.uk/
contact form|https://decipher.sanger.ac.uk/
email|decipher@sanger.ac.uk
online documentation|https://decipher.sanger.ac.uk/files/pdfs/decipher_database_flowchart.pdf
online documentation|https://decipher.sanger.ac.uk/files/pdfs/decipher_ethical_framework.pdf
Removed:
'dataProcesses' has been modified:
Before:
After:
Genome Browser
Phenotype Browser
Gene Browser
Gene Disorders Browser
CNV Syndromes Browser
Search
Login
Download
Added:
Genome Browser
Phenotype Browser
Gene Browser
Gene Disorders Browser
CNV Syndromes Browser
Search
Login
Download
Removed:
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 16:27, 03 Aug 2018 (approved):
'organizations' has been modified:
Before:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
After:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
Cambridge South REC, UK|https://www.hra.nhs.uk/about-us/committees-and-services/res-and-recs/search-research-ethics-committees/|Funds
Added:
Cambridge South REC, UK|https://www.hra.nhs.uk/about-us/committees-and-services/res-and-recs/search-research-ethics-committees/|Funds
Removed:
'grants' has been modified:
Before:
WT077008
After:
04/MRE05/50
WT077008
Added:
04/MRE05/50
Removed:
Edits to 'https://fairsharing.org/FAIRsharing.l8Sf5x' by 'The FAIRsharing Team' at 16:22, 03 Aug 2018 (approved):
'related_databases' has been modified:
Before:
After:
Pfam Protein Families
Integrated resource of protein families, domains and functional sites
Ensembl
Online Mendelian Inheritance in Man
Added:
Pfam Protein Families
Integrated resource of protein families, domains and functional sites
Ensembl
Online Mendelian Inheritance in Man
Removed:
'organizations' has been modified:
Before:
After:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
Added:
The Wellcome Trust, UK|https://wellcome.ac.uk|Funds
Removed:
'grants' has been modified:
Before:
After:
WT077008
Added:
WT077008
Removed:
'publications' has been modified:
Before:
After:
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation.|Bragin E,Chatzimichali EA,Wright CF,Hurles ME,Firth HV,Bevan AP,Swaminathan GJ|Nucleic Acids Res|2013
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.|Firth HV,Richards SM,Bevan AP,Clayton S,Corpas M,Rajan D,Van Vooren S,Moreau Y,Pettett RM,Carter NP|Am J Hum Genet|2009
Added:
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation.|Bragin E,Chatzimichali EA,Wright CF,Hurles ME,Firth HV,Bevan AP,Swaminathan GJ|Nucleic Acids Res|2013
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.|Firth HV,Richards SM,Bevan AP,Clayton S,Corpas M,Rajan D,Van Vooren S,Moreau Y,Pettett RM,Carter NP|Am J Hum Genet|2009
Removed: