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Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”
Author(s) -
Ryan Allison,
Martin Kimberly A.
Publication year - 2017
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.5072
Subject(s) - whole genome sequencing , single nucleotide polymorphism , cell free fetal dna , trisomy , snp , computational biology , dna sequencing , genetics , biology , genome , prenatal diagnosis , fetus , dna , genotype , pregnancy , gene
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