TEST DIRECTORY

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Laboratory：Akiruno

○HemeSight (hematopoietic tumor gene panel)

CODE：00L94 6

  • TEST NAME SPECIMEN
    REQUIREMENT
    （ｍL）     CONTAINER CAP COLOR STORE
    TEMPERATURE
    (STABILITY)     TURNAROUND
    TIME (DAY)     METHODOLOGY REFERENCE RANGE
    (UNIT)
  • Specified days
    HemeSight (hematopoietic tumor gene panel)
    Tumor
    and
    normal area
    See below
    See below refer to the following
     Please contact us in advance. Next Generation Sequencing (NGS)

    A method that uses a next-generation sequencer to simultaneously determine the base sequences of a huge number of DNA fragments.

COMMENT


Acceptable days are from Monday to Friday.
When requesting this test, please be sure to submit both tumor and normal area specimens in pairs at the same time.
The tumor specimen should be one of the following: blood, bone marrow fluid, unstained specimen slides, or fresh specimen. The tumor specimen must contain at least 20% tumor cells.

For the normal area, one of the following should be submitted: oral mucosa or fingernail.

Specimens from tumor and normal areas should be collected and stored in accordance with specimen handling guidelines, etc. (e.g., Rules for Handling Tissue Specimens for Genomic Medicine: prepared by the Japanese Society of Pathology, Specimen Quality Control Manual: prepared by the Japanese Council on Clinical Laboratory Standards, etc.).
Please avoid duplicate requests with other items. This testing method increases the influence of contamination, so please be careful when handling the specimen. The number of days required may vary depending on the measurement and analysis situation.

After applying for a HemeSight Portal account in advance, submit a request in accordance with the “HemeSight Portal Instruction Manual”.

An account registration is required to make a request, and a request form and specimen label must be submitted from the HemeSight Portal.
Both interim and final inspection reports must be received from the HemeSight Portal.
The interim report is expected to require 7 to 11 days. However, this does not apply to cases where a part of the process is repeated or additional confirmation is required due to the nature of the specimen or other reasons. This is also subject to the status of specimen requests, so please contact us if you are in a hurry.
●About requesting this test
When requesting this test, following explanation of the purpose and limitations of the test and confirmation that the subject's written consent has been obtained, use the dedicated request form output from the HemeSight Portal.
●How to make a request
1. Access the dedicated request entry site (HemeSight Portal).
2. After logging in, enter the necessary request information. *The subject's consent for the test must also be checked.
3. After inputting the necessary information, print out the dedicated request form and the specimen label.
4. Attach the label to the specimen and submit the specimen together with the dedicated request form.
* Internet connection is required.

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