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■ Search Result - Abbreviation : SNVs

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Abbreviation: SNVs
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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
single nucleotide variants
(607 times)
Genetics, Medical
(69 times)
CNVs (62 times)
NGS (56 times)
WGS (40 times)
2002 High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia.
single nucleotide variations
(162 times)
(26 times)
NGS (17 times)
CNVs (15 times)
WGS (8 times)
2005 Variation analysis of the severe acute respiratory syndrome coronavirus putative non-structural protein 2 gene and construction of three-dimensional model.
systemic necrotizing vasculitides
(4 times)
(2 times)
MPA (2 times)
PAN (2 times)
AAVs (1 time)
2011 Pregnancies in systemic necrotizing vasculitides: report on 12 women and their 20 pregnancies.
sequence variants
(2 times)
Medical Informatics
(1 time)
BMD (1 time)
CHARGE (1 time)
CNV (1 time)
2009 Inferring relative proportions of DNA variants from sequencing electropherograms.
sequencing of identified variants
(1 time)
(1 time)
DNMBP (1 time)
2016 Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24.
signature variation residues
(1 time)
(1 time)
SARS (1 time)
2005 Molecular evolution analysis and geographic investigation of severe acute respiratory syndrome coronavirus-like virus in palm civets at an animal market and on farms.
silicon nanovectors
(1 time)
(1 time)
Si (1 time)
2011 Size of the nanovectors determines the transplacental passage in pregnancy: study in rats.
single nt variants
(1 time)
Communicable Diseases
(1 time)
MLVA (1 time)
PCR (1 time)
PFGE (1 time)
2015 The utility of multiple molecular methods including whole genome sequencing as tools to differentiate Escherichia coli O157:H7 outbreaks.
specific mutations -single-nucleotide variations
(1 time)
Medical Informatics
(1 time)
SNPs (1 time)
SVs (1 time)
2018 Comparing the performance of selected variant callers using synthetic data and genome segmentation.
10  variations-single nucleotide variants
(1 time)
(1 time)
aCGH (1 time)
ASD (1 time)
CNVs (1 time)
2017 Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.