Record added: Aug. 3, 2018, 2:58 p.m.
Record updated: Oct. 17, 2018, 5:19 p.m. by The FAIRsharing Team.

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: