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Abbreviation: SNVs
Appearance Frequency: 1660 time(s)
Long forms: 17

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
single nucleotide variants
(1638 times)
Genetics, Medical
(165 times)
CNVs (201 times)
NGS (158 times)
WGS (99 times)
2002 High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia.
systemic necrotizing vasculitides
(5 times)
(2 times)
MPA (2 times)
PAN (2 times)
AAVs (1 time)
2010 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.
spanlastic nanovesicles
(2 times)
Drug Therapy
(2 times)
AKBA (1 time)
DSC (1 time)
EA (1 time)
2019 Transdermal delivery of fluvastatin sodium via tailored spanlastic nanovesicles: mitigated Freund's adjuvant-induced rheumatoid arthritis in rats through suppressing p38 MAPK signaling pathway.
seed-derived nanovesicles
(1 time)
(1 time)
DSS (1 time)
HNVs (1 time)
HSNVs (1 time)
2022 Hemp-Derived Nanovesicles Protect Leaky Gut and Liver Injury in Dextran Sodium Sulfate-Induced Colitis.
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.
Seven variations of a single nucleotide
(1 time)
(1 time)
INSL3 (1 time)
PCR (1 time)
UTR (1 time)
2019 Novel combined insulin-like 3 variations of a single nucleotide in cryptorchidism.
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.
10  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.
11  single nucleotide variants and polymorphisms
(1 time)
(1 time)
OCA (1 time)
TYR (1 time)
2021 Biophysical Compatibility of a Heterotrimeric Tyrosinase-TYRP1-TYRP2 Metalloenzyme Complex.
12  Single number variants
(1 time)
(1 time)
apoB (2 times)
ACS (1 time)
CG (1 time)
2022 Analysis of the APOB Gene and Apolipoprotein B Serum Levels in a Mexican Population with Acute Coronary Syndrome: Association with the Single Nucleotide Variants rs1469513, rs673548, rs676210, and rs1042034.
13  single-variant polymorphisms
(1 time)
Natural Science Disciplines
(1 time)
PCR-RFLP (1 time)
2021 Genetic polymorphisms of inflammasome genes associated with pediatric acute lymphoblastic leukemia and clinical prognosis in the Brazilian Amazon.
14  SNVs, also known as single nucleotide polymorphisms
(1 time)
Natural Science Disciplines
(1 time)
GWAS (1 time)
2021 Reproducibility in the UK biobank of genome-wide significant signals discovered in earlier genome-wide association studies.
15  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.
16  standard normal variables
(1 time)
BP-ANN (1 time)
PCA (1 time)
SVM (1 time)
2022 A Method for Capture and Detection of Crop Airborne Disease Spores Based on Microfluidic Chips and Micro Raman Spectroscopy.
17  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.