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. 2014 Sep 3;3(3):972–985. doi: 10.3390/jcm3030972

Table 2.

Some distinctive and common qualities in the comparison of fetal cell and cell free DNA based prenatal testing.

Question DNA Source Distinctive Qualities Common Qualities
What are the instrument needs? Fetal Cells Cell sorting
Microscopes
Cell culture (?)
CGH-SNP Platform
PCR related
NextGen Sequencing
Fetal Cell-Free DNA DNA isolation
Mass spectrometer
What are the advantageous capabilities? Fetal Cells Potential to be a diagnostic test and not limited to screening
Direct analysis of single (?) or pooled (?) cells using biological measurements
Amenable to FISH and/or qfPCR analyses for rapid analysis of aneuploidy
Capacity for single gene analysis, variation screening or sequencing
Potential for functional and polygenic analyses
Amenable to CNV (copy number variation) determinations by CGH-SNP analysis
Non-invasive
Capacity for both aneuploidy and CNV analyses
Fetal Cell-Free DNA Preparation more rapid than cells
Minimal problems in transporting blood from clinic to centralized labs
Potential for CNV determinations by deep sequencing and analysis
What are the apparent disadvantages or important challenges to be met? Fetal Cells Isolation of cells may be labor intensive; cost effective throughput has not been demonstrated
Integrity of DNA in possibly apoptotic cells may dictate consistency and quantity of cells required for reliable evaluations
Requires faithful and complete amplification of DNA
Likely to be few cells analyzed from a sample and thus less likely to be representative of a mosaic condition
Stability and integrity maintenance requirements for transport of cells from phlebotomist to laboratory
Requisite equipment and expertise may limit distribution beyond centralized laboratories
Fetal Cell-Free DNA Becoming validated as an effective diagnostic as well as screening test
Accuracy seems to depend on level of proportion of extracted DNA derived from fetus
Results are based on (powerful) statistical methods rather than direct biological measurements
Unable to determine mosaicism if present
Degree of extension of analyses beyond aneuploidy yet to be determined and validated