Analysis of nucleic acids is playing an increasing role in the diagnosis and management of patients with hematopoietic
neoplasms. The tests include those for detection of clonality by analysis of gene rearrangements in the antigen receptor genes or
detection of nonrandom inactivation of the X chromosome, detection and quantification of junctions formed by chromosomal
translocations, detection of micromutations, quantification of chimerism after allogeneic hematopoietic transplantation, and
quantification of normal DNA or RNA sequences. The methods used in clinical molecular hematopathology include end-point
PCR, reverse-transcriptase PCR, real-time fluorescence-based PCR, DNA sequencing, FISH, and hybridization-based microarray
and microbead assays.
Clinical and Laboratory Standards Institute document MM05-A2 - Nucleic Acid Amplification Assays for Molecular
Hematopathology; Approved Guideline - Second Edition addresses the needs of the laboratory by providing recommendations on
a variety of laboratory tests based on analysis of nucleic acids. It addresses preexamination and examination issues affecting
assay performance, reporting of laboratory results, and QA. The guideline is designed to assist a molecular diagnostic laboratory
in acquiring a new assay or new technology, as well as serve as a refresher for those already experienced with a particular area of
analysis.
Document identifier
CLSI MM05-A2 (R2018)
Title
Nucleic Acid Amplification Assays for Molecular Hematopathology; Approved Guideline-Second Edition,MM05A2E
CLSI Category
Molecular Methods
Publication date
2012-03-01
International Relationship
History of version
CLSI MM05-A2 (R2018) * CLSI MM05A
Price |
140 vnd |