TY - JOUR
T1 - Towards systematic nomenclature for cell-free DNA
AU - Bronkhorst, Abel J.
AU - Ungerer, Vida
AU - Diehl, Frank
AU - Anker, Philippe
AU - Dor, Yuval
AU - Fleischhacker, Michael
AU - Gahan, Peter B.
AU - Hui, Lisa
AU - Holdenrieder, Stefan
AU - Thierry, Alain R.
N1 - Publisher Copyright: © 2020, The Author(s).
PY - 2021/4
Y1 - 2021/4
N2 - Cell-free DNA (cfDNA) has become widely recognized as a promising candidate biomarker for minimally invasive characterization of various genomic disorders and other clinical scenarios. However, among the obstacles that currently challenge the general progression of the research field, there remains an unmet need for unambiguous universal cfDNA nomenclature. To address this shortcoming, we classify in this report the different types of cfDNA molecules that occur in the human body based on its origin, genetic traits, and locality. We proceed by assigning existing terms to each of these cfDNA subtypes, while proposing new terms and abbreviations where clarity is lacking and more precise stratification would be beneficial. We then suggest the proper usage of these terms within different contexts and scenarios, focusing mainly on the nomenclature as it relates to the domains of oncology, prenatal testing, and post-transplant surgery surveillance. We hope that these recommendations will serve as useful considerations towards the establishment of universal cfDNA nomenclature in the future. In addition, it is conceivable that many of these recommendations can be transposed to cell-free RNA nomenclature by simply exchanging “DNA” with “RNA” in each acronym/abbreviation. Similarly, when describing DNA and RNA collectively, the suffix can be replaced with “NAs” to indicate nucleic acids.
AB - Cell-free DNA (cfDNA) has become widely recognized as a promising candidate biomarker for minimally invasive characterization of various genomic disorders and other clinical scenarios. However, among the obstacles that currently challenge the general progression of the research field, there remains an unmet need for unambiguous universal cfDNA nomenclature. To address this shortcoming, we classify in this report the different types of cfDNA molecules that occur in the human body based on its origin, genetic traits, and locality. We proceed by assigning existing terms to each of these cfDNA subtypes, while proposing new terms and abbreviations where clarity is lacking and more precise stratification would be beneficial. We then suggest the proper usage of these terms within different contexts and scenarios, focusing mainly on the nomenclature as it relates to the domains of oncology, prenatal testing, and post-transplant surgery surveillance. We hope that these recommendations will serve as useful considerations towards the establishment of universal cfDNA nomenclature in the future. In addition, it is conceivable that many of these recommendations can be transposed to cell-free RNA nomenclature by simply exchanging “DNA” with “RNA” in each acronym/abbreviation. Similarly, when describing DNA and RNA collectively, the suffix can be replaced with “NAs” to indicate nucleic acids.
UR - http://www.scopus.com/inward/record.url?scp=85094208055&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/s00439-020-02227-2
DO - https://doi.org/10.1007/s00439-020-02227-2
M3 - مقالة مرجعية
C2 - 33123832
SN - 0340-6717
VL - 140
SP - 565
EP - 578
JO - Human Genetics
JF - Human Genetics
IS - 4
ER -