Record updated: July 18, 2017, 12:16 p.m. by The FAIRsharing Team.

Edits to 'https://fairsharing.org/FAIRsharing.xk98ez' by 'The FAIRsharing Team' at 13:56, 11 Jul 2017 (approved):

	'shortname' has been modified:
		Before: ngd
		After: 

            

Edits to 'https://fairsharing.org/FAIRsharing.xk98ez' by 'The FAIRsharing Team' at 09:40, 28 Nov 2016 (approved):

	'description' has been modified:
		Before: The NimbleGen Gene Description is a text tabular format that contains descriptive information (annotation) about the genes on an array design. 
		After: The NimbleGen Gene Description is a text tabular format that contains descriptive information (annotation) about the genes on an array. 

            

Edits to 'https://fairsharing.org/FAIRsharing.xk98ez' by 'The FAIRsharing Team' at 05:06, 26 Nov 2016 (approved):

	'homepage' has been modified:
		Before: http://www.nimblegen.com/products/methylation/dataguide/index.html
		After: https://dmac.cbs.dtu.dk/service/data-formats

            

Edits to 'https://fairsharing.org/FAIRsharing.xk98ez' by 'The FAIRsharing Team' at 09:58, 22 Oct 2016 (approved):

	'description' has been modified:
		Before: "Nimblegen Gene Data Format" is a standard, specialising in the fields described under "scope and data types", below. Until this entry is claimed, more information on this project can be found at http://www.nimblegen.com/products/methylation/dataguide/index.html. This text was generated automatically. If you work on the project responsible for "Nimblegen Gene Data Format" then please consider helping us  by claiming this record  and updating it appropriately.
		After: Roche NimbleGen is an innovator in genomics focused on developing target enrichment solutions for next-generation sequencing. NimbleGen technologies allow researchers to selectively target DNA sequences of interest in their genome of interest, human or non-human, either through focused exomes or custom designed gene panels, for variant discovery and validation. With a suite of tools for targeted DNA sequencing, bi-sulfite sequencing and transcriptome sequencing, we are enabling the life science community to achieve their research goals more efficiently in order to understand the association genomics and epigenomics have with diseases and biological processes. Countries have changed:  Previous values: New values:  USA Taxonomy list has changed:  Previous values: New values:  All|http://identifiers.org/taxonomy/1?resource=MIR:00100019 Support links have changed:  Previous values: New values:  http://sequencing.roche.com/contact-us.html