Skip to Content
Merck
All Photos(1)

Documents

NIST8392

Human DNA for Whole-Genome Variant Assessment (Family Trio of Eastern European Ashkenazi Jewish Ancestry) (HG-002, HG-003, HG-004)

NIST®SRM®

Synonym(s):

Human DNA for Variant Calling (Ashkenazi Jewish) (HG-002, HG-003, HG-004)

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
41116107
NACRES:
NA.24

form

liquid

packaging

pkg of 10 μg (3 vials)

manufacturer/tradename

NIST®

application(s)

genomic analysis

storage temp.

−20°C

General description

Human DNA for Whole-Genome Variant Assessment Reference Material (RM) is intended for validation, optimization, and process evaluation purposes. It consists of three human whole genome samples from a son-father-mother family trio of Eastern European Ashkenazi Jewish ancestry from the Personal Genome Project (IDs huAA53E0, hu6E4515, and hu8E87A9). A unit of RM 8392 consists of three vials containing human genomic DNA from a specific family member; extracted from three large growths of human lymphoblastoid cell lines from the Coriell Institute for Medical Research (Camden, NJ): GM24385 (son) labeled as HG-002, GM24149 (father) labeled as HG-003, and GM24143 (mother) labeled as HG-004. Each vial contains approximately 10 µg of genomic DNA, and the DNA is in TE buffer (10 mM TRIS, 1 mM EDTA, pH 8.0)

SRM 8392_cert

SRM 8392_SDS

Application

Human DNA for Whole-Genome Variant Assessment Reference Material is intended for assessing the performance of human genome sequencing variant calling by obtaining estimates of true positives, false positives, and false negatives. Sequencing applications could include:

  • whole genome sequencing
  • whole exome sequencing
  • targeted sequencing such as gene panels

Features and Benefits

  • This reference material contains isolated DNA rather than live cells and is intended for research use.
  • An extensive report of the investigation is available through NIST
  • Information values are provided for single nucleotide variations (SNVs), small insertions and deletions (indels), and homozygous reference genotypes.

Other Notes

  • RM 8392 is stored at –20 °C at NIST but will be shipped in freezer packs and may not arrive frozen.
  • Details on expiration, storage, safety, usage, and source are provided in the NIST certificate.
  • Information on biomaterials, disposal, and transport is available in the SDS.
  • he size distributions are measured using PFGE, and biases of this method were not characterized.

Legal Information

NIST is a registered trademark of National Institute of Standards and Technology
SRM is a registered trademark of National Institute of Standards and Technology

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Bennett O V Shum et al.
The Journal of molecular diagnostics : JMD, 19(4), 602-612 (2017-05-16)
The sensitivity and specificity of next-generation sequencing laboratory developed tests (LDTs) are typically determined by an analyte-specific approach. Analyte-specific validations use disease-specific controls to assess an LDT's ability to detect known pathogenic variants. Alternatively, a methods-based approach can be used
Determining Performance Metrics for Targeted Next-Generation Sequencing Panels Using Reference Materials
Cleveland MH, et al.
The Journal of Molecular Diagnostics : JMD, 20, 583-590 (2018)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service