Comment on "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods"
Prenat Diagn
.
2017 Jul;37(7):725-726.
doi: 10.1002/pd.5072.
Authors
Allison Ryan
1
,
Kimberly A Martin
2
Affiliations
1
Natera Statistics, San Carlos, CA, USA.
2
Natera, San Carlos, CA, USA.
PMID:
28675625
PMCID:
PMC5575504
DOI:
10.1002/pd.5072
No abstract available
Publication types
Letter
Comment
MeSH terms
DNA
Female
Fetus*
High-Throughput Nucleotide Sequencing
Humans
Nucleotides
Polymorphism, Single Nucleotide
Pregnancy
Prenatal Diagnosis*
Sequence Analysis, DNA
Substances
Nucleotides
DNA