Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods"
Prenat Diagn
.
2017 Jul;37(7):727-728.
doi: 10.1002/pd.5071.
Authors
Dale Muzzey
1
,
Carrie Haverty
1
,
Eric A Evans
1
,
James D Goldberg
1
Affiliation
1
Counsyl Inc., South San Francisco, CA, USA.
PMID:
28675624
PMCID:
PMC5811916
DOI:
10.1002/pd.5071
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