The research
Scientific field, completed studies or experimental programs and acquisition period. Include the material families, biological systems or methods represented.
Existing experimental collections may be relevant to teams developing scientific AI. Describe the data already held by your organization, the records that connect it and who can discuss a licence.
An archive is easier to assess when its measurements can be understood in context. Start with a description of what exists today.
Scientific field, completed studies or experimental programs and acquisition period. Include the material families, biological systems or methods represented.
Approximate volume, number of samples or experiments, measurement types and file formats. Counts of independent records help explain what a large archive contains.
How raw files connect to preparation, methods, measurements, labels and results. Describe the identifiers that connect records across instruments or studies.
Controls, replicates, unsuccessful runs and relevant variations. Describe exclusions and incomplete records rather than assuming every series is complete.
Data dictionaries, method descriptions, acquisition settings and other existing documentation. Identify any preparation or explanation that a review would require.
Who holds the collection and who coordinates licensing discussions. Equipment ownership and permission to license its stored research data are separate questions.
Process history + measurements + results
A completed experimental program may hold synthesis records, characterization files and property measurements connected by sample identifiers. Describe those relationships, approximate scope and any gaps.
Study structure + measurements + labels
A completed research study may hold molecular outputs or images alongside preparation methods, annotations and experimental outcomes. Start with aggregate scope and the available relationships.
A description does not commit you to share files or grant a licence. Terms are specific to the transaction.
SIB reviews the description against an acquisition requirement and identifies the technical questions that need clarification.
Where appropriate, discuss the information or bounded sample needed to assess suitability. The purpose, recipient and access arrangements are settled before anything moves.
The discussion can cover permitted use, the included records and the holder’s interests in the collection. Do not assume the same terms apply to every dataset.
Agree any preparation work, acceptance criteria and transfer arrangements as part of the transaction. File volume alone does not define the scope.
Leave patient records, research images and confidential dataset files out of the initial website enquiry. Any later sample review and transfer are arranged separately.
Tell us the field, approximate scope, methods and connected records. We can identify the next questions together.