This is a table of type bigram and their frequencies. Use it to search & browse the list to learn more about your study carrel.
bigram | frequency |
---|---|
isothermal amplification | 908 |
mediated isothermal | 784 |
lamp assay | 653 |
nucleic acid | 330 |
reverse transcription | 307 |
rapid detection | 261 |
lamp reaction | 213 |
transcription loop | 158 |
clinical samples | 154 |
dna polymerase | 140 |
rna extraction | 137 |
chain reaction | 134 |
viral rna | 134 |
time pcr | 130 |
respiratory syndrome | 125 |
lamp method | 118 |
lamp assays | 117 |
amplification method | 114 |
agarose gel | 111 |
polymerase chain | 110 |
nucleic acids | 105 |
amplification assay | 103 |
acute respiratory | 102 |
acid amplification | 97 |
detection limit | 94 |
gel electrophoresis | 92 |
severe acute | 91 |
granted medrxiv | 88 |
author funder | 88 |
dna amplification | 87 |
lamp primers | 87 |
copyright holder | 86 |
sybr green | 85 |
primer sets | 85 |
reverse transcriptase | 84 |
loop primers | 81 |
primer set | 79 |
time rt | 79 |
version posted | 77 |
novel coronavirus | 76 |
conventional rt | 76 |
syndrome coronavirus | 76 |
lamp products | 75 |
lamp reactions | 74 |
amplifi cation | 73 |
reaction mixture | 70 |
pcr assay | 69 |
positive samples | 68 |
real time | 68 |
peer review | 66 |
strand displacement | 65 |
virus infection | 65 |
doc id | 63 |
cord uid | 63 |
infectious diseases | 63 |
visual detection | 61 |
green i | 61 |
time reverse | 60 |
amplification reaction | 60 |
high sensitivity | 60 |
positive results | 60 |
dna extraction | 59 |
rapid diagnosis | 57 |
zika virus | 56 |
loop mediated | 56 |
loopmediated isothermal | 56 |
viral load | 56 |
lateral flow | 55 |
medrxiv preprint | 55 |
japanese encephalitis | 53 |
qpcr assay | 53 |
magnetic bead | 53 |
target dna | 53 |
clinical specimens | 51 |
isothermal conditions | 50 |
based amplification | 50 |
negative samples | 48 |
influenza virus | 48 |
detection method | 48 |
dengue virus | 47 |
rna polymerase | 47 |
magnesium pyrophosphate | 47 |
reaction time | 46 |
based detection | 46 |
water bath | 45 |
swab samples | 45 |
color change | 45 |
mycobacterium tuberculosis | 45 |
per reaction | 45 |
using loop | 45 |
virus isolation | 44 |
ct values | 44 |
blood samples | 43 |
conventional pcr | 43 |
new england | 42 |
performed using | 42 |
whole blood | 42 |
orf ab | 41 |
lamp primer | 41 |
copies per | 41 |
escherichia coli | 41 |
master mix | 41 |
detection methods | 41 |
inner primer | 41 |
west nile | 40 |
england biolabs | 40 |
negative control | 40 |
bst dna | 40 |
cell death | 40 |
dna synthesis | 39 |
target sequence | 39 |
sample preparation | 39 |
disease virus | 39 |
nasopharyngeal swabs | 39 |
serial dilutions | 38 |
copy number | 38 |
specific primers | 38 |
acid sequence | 37 |
public health | 37 |
amplification using | 36 |
free water | 36 |
high specificity | 36 |
molecular detection | 36 |
naked eye | 36 |
qlamp assay | 36 |
copies reaction | 36 |
acid testing | 36 |
specific amplification | 35 |
encephalitis virus | 34 |
porcine circovirus | 34 |
reaction temperature | 34 |
highly specific | 34 |
outer primers | 34 |
pcr assays | 34 |
lamp amplification | 34 |
ethidium bromide | 33 |
positive control | 33 |
rna viruses | 33 |
amplification products | 32 |
time detection | 32 |
present study | 32 |
total rna | 32 |
step rt | 32 |
coronavirus disease | 32 |
serum samples | 31 |
inner primers | 31 |
sensitive detection | 31 |
patient samples | 31 |
false positives | 31 |
swab specimens | 31 |
porcine parvovirus | 31 |
sputum samples | 31 |
clinical diagnosis | 31 |
made available | 30 |
rights reserved | 30 |
cancer cells | 30 |
higher sensitivity | 30 |
lamp detection | 30 |
highly sensitive | 30 |
je virus | 30 |
reaction volume | 30 |
nile virus | 30 |
reaction mixtures | 30 |
reuse allowed | 29 |
amplified products | 29 |
standard curve | 29 |
eiken chemical | 29 |
direct detection | 29 |
constant temperature | 29 |
international license | 29 |
room temperature | 29 |
time monitoring | 29 |
rna isolation | 29 |
nested rt | 29 |
primer design | 29 |
without permission | 29 |
allowed without | 29 |
primers targeting | 29 |
chik virus | 28 |
polymerase amplification | 28 |
amplification efficiency | 28 |
applied biosystems | 28 |
avian influenza | 28 |
genomic dna | 28 |
dried blood | 28 |
bead rna | 28 |
primer mix | 28 |
rna samples | 28 |
fold serial | 28 |
detection system | 28 |
colorimetric lamp | 28 |
viral nucleic | 28 |
recombinase polymerase | 28 |
negative controls | 28 |
six primers | 28 |
using rt | 27 |
posted november | 27 |
dna template | 27 |
syndrome virus | 27 |
results showed | 27 |
colorimetric rt | 27 |
false positive | 27 |
detection using | 27 |
isothermal nucleic | 27 |
acid detection | 26 |
stranded dna | 26 |
virus detection | 26 |
widely used | 26 |
commercially available | 26 |
mycobacterium ulcerans | 26 |
infectious peritonitis | 26 |
molecular diagnostics | 26 |
feline infectious | 26 |
magnetic beads | 25 |
specific lamp | 25 |
target rna | 25 |
samples collected | 25 |
copy numbers | 25 |
microfluidic disc | 25 |
diagnostic test | 25 |
rna template | 25 |
diagnostic methods | 25 |
pcr methods | 25 |
newly developed | 25 |
assay using | 25 |
specific detection | 25 |
novel loop | 24 |
molecular diagnostic | 24 |
optimal reaction | 24 |
specific rt | 24 |
pathogen detection | 24 |
buruli ulcer | 24 |
respiratory viruses | 24 |
extraction kit | 24 |
middle east | 24 |
loop primer | 24 |
amplification techniques | 24 |
snp detection | 24 |
detecting sars | 24 |
isothermal amplifi | 23 |
lung cancer | 23 |
east respiratory | 23 |
detection results | 23 |
developing countries | 23 |
united states | 23 |
accelerated reaction | 23 |
outer primer | 23 |
gold standard | 23 |
diagnostic method | 23 |
fluorescence signal | 23 |
rna detection | 23 |
reaction tube | 23 |
influenza viruses | 23 |
detection rate | 23 |
human papillomavirus | 23 |
circovirus type | 23 |
herpes simplex | 23 |
microfluidic system | 22 |
pcr amplification | 22 |
pcr products | 22 |
armored rna | 22 |
simplex virus | 22 |
primer explorer | 22 |
sample types | 22 |
newcastle disease | 22 |
colorimetric detection | 22 |
lamp system | 22 |
fever virus | 22 |
four primers | 22 |
chikungunya virus | 22 |
linked immunosorbent | 22 |
conventional lamp | 22 |
urine samples | 21 |
well plate | 21 |
posted july | 21 |
rna particles | 21 |
virus serotypes | 21 |
lysis buffer | 21 |
nasopharyngeal swab | 21 |
two outer | 21 |
qpcr assays | 21 |
nested pcr | 21 |
using clinical | 21 |
feline coronavirus | 21 |
chemical co | 21 |
viral genome | 21 |
lamp test | 21 |
virus rna | 20 |
copies ml | 20 |
african genotype | 20 |
lamp results | 20 |
induced autophagy | 20 |
egfr mutations | 20 |
amplification technique | 20 |
generation sequencing | 20 |
within min | 20 |
blood spots | 20 |
gene amplification | 20 |
virus type | 20 |
displacement activity | 20 |
dilution series | 20 |
reaction mix | 20 |
detect sars | 20 |
diagnostic laboratory | 20 |
primers used | 20 |
mediated autophagy | 20 |
viral infections | 20 |
pcr method | 19 |
gene sequences | 19 |
gargle lavage | 19 |
intravenous alteplase | 19 |
described previously | 19 |
pcr kit | 19 |
authors declare | 19 |
infected shrimp | 19 |
igg antibodies | 19 |
infected patients | 19 |
peripheral blood | 19 |
purified dna | 19 |
assay developed | 19 |
rna virus | 19 |
listeria monocytogenes | 19 |
displacement amplification | 19 |
iu ml | 19 |
fluorescent dye | 19 |
dna products | 19 |
rna extracted | 19 |
fluorescence detection | 18 |
copies tube | 18 |
time fluorescence | 18 |
turbidity derived | 18 |
genbank accession | 18 |
posted may | 18 |
clinical diagnostic | 18 |
lamp product | 18 |
carotid artery | 18 |
mm tris | 18 |
hybridization chain | 18 |
amplification assays | 18 |
accession number | 18 |
immunosorbent assay | 18 |
ct value | 18 |
pyrophosphate formation | 18 |
extracted rna | 18 |
template dna | 18 |
positive result | 18 |
supplementary table | 18 |
positive reaction | 18 |
using reverse | 18 |
isothermal dna | 18 |
thermal cycler | 18 |
pocket warmer | 18 |
amplified dna | 18 |
hbv dna | 18 |
lamp amplicons | 18 |
false negatives | 17 |
hpv type | 17 |
developed rt | 17 |
amplification rapid | 17 |
rolling circle | 17 |
induces autophagy | 17 |
target gene | 17 |
filter paper | 17 |
limited settings | 17 |
diagnostic tool | 17 |
distinct regions | 17 |
amplification methods | 17 |
samples using | 17 |
visual inspection | 17 |
viral dna | 17 |
direct naats | 17 |
detection sensitivity | 17 |
virus rapid | 17 |
denv infection | 17 |
uv light | 17 |
base apparatus | 17 |
backward inner | 17 |
displacement dna | 17 |
results indicated | 17 |
host cell | 17 |
clinical signs | 17 |
forward inner | 17 |
infectious bronchitis | 17 |
pcr system | 17 |
transmissible gastroenteritis | 17 |
isolated rna | 17 |
acute phase | 17 |
less sensitive | 17 |
molecular diagnosis | 17 |
using lamp | 17 |
thermal cycling | 17 |
rna copies | 16 |
sry gene | 16 |
amplification detection | 16 |
circle amplification | 16 |
opiph system | 16 |
without rna | 16 |
detect viral | 16 |
viral replication | 16 |
assay showed | 16 |
one step | 16 |
detection limits | 16 |
specific dna | 16 |
vhs virus | 16 |
target sequences | 16 |
hpv dna | 16 |
fecal samples | 16 |
reaction tubes | 16 |
situ rt | 16 |
wasting syndrome | 16 |
coronavirus sars | 16 |
disease control | 16 |
alteplase infusion | 16 |
world health | 16 |
rna using | 16 |
syncytial virus | 16 |
using primer | 16 |
two loop | 16 |
respiratory syncytial | 16 |
tested positive | 16 |
designed using | 16 |
based assays | 16 |
obtained using | 16 |
laboratory diagnosis | 16 |
stranded rna | 16 |
expensive equipment | 16 |
health organization | 16 |
early diagnosis | 16 |
lamp reagents | 16 |
quantitative pcr | 15 |
serially diluted | 15 |
qpcr using | 15 |
cancer cell | 15 |
thermo fisher | 15 |
hcv rna | 15 |
total volume | 15 |
positive reactions | 15 |
simple visual | 15 |
tested using | 15 |
induce autophagy | 15 |
crispr cas | 15 |
multisystemic wasting | 15 |
commonly used | 15 |
dna sequences | 15 |
diagnostic accuracy | 15 |
hbv lamp | 15 |
acid extraction | 15 |
bronchitis virus | 15 |
immunodeficiency virus | 15 |
visual rt | 15 |
immune system | 15 |
isothermal device | 15 |
cell culture | 15 |
dependent amplification | 15 |
phenol red | 15 |
multiplex pcr | 15 |
lamp protocol | 15 |
ab gene | 15 |
turkey coronavirus | 15 |
ischemic stroke | 15 |
tuberculosis complex | 15 |
clinical sample | 15 |
negative results | 15 |
serotype specific | 15 |
novel rt | 15 |
centrifugal microfluidic | 15 |
great potential | 15 |
iso buffer | 15 |
dna fragments | 15 |
predictive value | 15 |
host cells | 15 |
direct pcr | 15 |
human immunodeficiency | 15 |
analytical sensitivity | 14 |
rapid diagnostic | 14 |
cost effective | 14 |
distilled water | 14 |
large numbers | 14 |
conserved region | 14 |
rapid molecular | 14 |
suspected covid | 14 |
binding proteins | 14 |
upper respiratory | 14 |
amplification technologies | 14 |
informed consent | 14 |
pharyngeal swab | 14 |
rapid identification | 14 |
dna purification | 14 |
quantitative rt | 14 |
diagnostic testing | 14 |
viral pathogens | 14 |
restriction enzyme | 14 |
rainbow trout | 14 |
fisher scientific | 14 |
reaction buffer | 14 |
assay detection | 14 |
ebola virus | 14 |
hydroxynaphthol blue | 14 |
clinical trials | 14 |
based methods | 14 |
pcr detection | 14 |
postweaning multisystemic | 14 |
extraction protocol | 14 |
optical detection | 14 |
viral hemorrhagic | 14 |
previous studies | 14 |
coronavirus using | 14 |
dna extracts | 14 |
positive controls | 14 |
integrated isothermal | 14 |
viral infection | 14 |
results obtained | 14 |
autophagosome formation | 14 |
amplification test | 14 |
even though | 14 |
causative agent | 14 |
infectious disease | 13 |
dna detection | 13 |
nucleotide sequence | 13 |
swab sample | 13 |
heating block | 13 |
mm dntps | 13 |
final volume | 13 |
infected individuals | 13 |
detection assays | 13 |
pseudorabies virus | 13 |
confidence intervals | 13 |
dengue viruses | 13 |
body cavity | 13 |
deficient mice | 13 |
saliva samples | 13 |
porcine reproductive | 13 |
neurodegenerative diseases | 13 |
primer dimers | 13 |
elution buffer | 13 |
transcriptase polymerase | 13 |
reaction products | 13 |
time loop | 13 |
flow dipstick | 13 |
dna loop | 13 |
detecting ibv | 13 |
mini kit | 13 |
prv ge | 13 |
yellow head | 13 |
amplification kit | 13 |
selective autophagy | 13 |
viral loads | 13 |
diagnostic assays | 13 |
also tested | 13 |
detection kits | 13 |
ns antigen | 13 |
reaction conditions | 13 |
commercial rt | 13 |
pcr test | 13 |
care diagnostics | 13 |
conducted using | 13 |
heat block | 13 |
like pattern | 13 |
rna purification | 13 |
extraction methods | 13 |
sars coronavirus | 13 |
extracted using | 13 |
fl uorescent | 13 |
using real | 12 |
pharyngeal swabs | 12 |
tissue samples | 12 |
oxidative stress | 12 |
autophagy genes | 12 |
previous study | 12 |
conventional one | 12 |
temperature control | 12 |
detection mix | 12 |
mumps virus | 12 |
ns serotype | 12 |
genome sequences | 12 |
mediated amplification | 12 |
assays targeting | 12 |
foster city | 12 |
protease inhibitors | 12 |
transcription polymerase | 12 |
internal control | 12 |
sequence analysis | 12 |
hemorrhagic septicaemia | 12 |
dependent rna | 12 |
pcr results | 12 |
sample collection | 12 |
positive signal | 12 |
time quantitative | 12 |
polymerase activity | 12 |
vhs rna | 12 |
digital pcr | 12 |
head virus | 12 |
samples tested | 12 |
exponential amplification | 12 |
time points | 12 |
fimbriae gene | 12 |
negative predictive | 12 |
molecular methods | 12 |
tcid ml | 12 |
six distinct | 12 |
molecular assays | 12 |
virus replication | 12 |
designed primers | 12 |
ethics committee | 12 |
clinical symptoms | 12 |
detection systems | 12 |
test results | 12 |
ns ag | 12 |
cycle threshold | 12 |
time required | 12 |
qpcr detection | 12 |
based tests | 12 |
amplification curves | 12 |
critically ill | 12 |
poc diagnostics | 12 |
immune response | 12 |
swine fever | 12 |
gene sequence | 12 |
assay may | 12 |
necrosis virus | 12 |
nasal swabs | 12 |
detection time | 12 |
reaction using | 12 |
blood spot | 12 |
previously described | 11 |
lowest detection | 11 |
sex determination | 11 |
method rapid | 11 |
clinical application | 11 |
care testing | 11 |
clinical use | 11 |
results indicate | 11 |
gene detection | 11 |
agarose gels | 11 |
type prv | 11 |
assay development | 11 |
amplification process | 11 |
diagnostic tests | 11 |
rna molecules | 11 |
chamber iii | 11 |
diarrhea virus | 11 |
single reaction | 11 |
fold higher | 11 |
primers loop | 11 |
type strains | 11 |
digital lamp | 11 |
sensitivity test | 11 |
highly conserved | 11 |
single step | 11 |
salmonella enterica | 11 |
simultaneous detection | 11 |
oligonucleotide primers | 11 |
two primers | 11 |
mouth disease | 11 |
visualized using | 11 |
lymph nodes | 11 |
closely related | 11 |
rna standard | 11 |
single strand | 11 |
extraction method | 11 |
dna rna | 11 |
chlamydia trachomatis | 11 |
also known | 11 |
touchdown lamp | 11 |
serological tests | 11 |
samples obtained | 11 |
two assays | 11 |
mm mgso | 11 |
turnaround time | 11 |
chik fever | 11 |
virus genome | 11 |
false negative | 11 |
lamp technology | 11 |
gastroenteritis coronavirus | 11 |
disposable micro | 11 |
clinical validation | 11 |
pcr reaction | 11 |
total reaction | 11 |
amplified product | 11 |
assays using | 11 |
glu lys | 11 |
amplification time | 11 |
transport media | 11 |
two different | 11 |
serial dilution | 11 |
respiratory tract | 11 |
competing interests | 11 |
uvrd helicase | 11 |
new generation | 11 |
isothermal mastermix | 11 |
primer sequences | 11 |
human herpesvirus | 11 |
direct sequencing | 11 |
standard curves | 11 |
posted august | 11 |
amplification tests | 11 |
resource settings | 11 |
cell lung | 11 |
single tube | 11 |
porcine epidemic | 11 |
egfr mutation | 11 |
distinct sequences | 11 |
table ii | 10 |
human coronaviruses | 10 |
using primers | 10 |
bip primers | 10 |
specially designed | 10 |
two inner | 10 |
low viral | 10 |
complementary sequence | 10 |
uv transilluminator | 10 |
cohort i | 10 |
covert mortality | 10 |
test kit | 10 |
pcr product | 10 |
dna rapid | 10 |
factor receptor | 10 |
epidemic diarrhea | 10 |
inhibiting autophagy | 10 |
intercalating dye | 10 |
university hospital | 10 |
human genomic | 10 |
isothermal master | 10 |
autophagic vacuoles | 10 |
virol methods | 10 |
viral diseases | 10 |
epidermal growth | 10 |
copper plates | 10 |
spike protein | 10 |
lavage samples | 10 |
swine transmissible | 10 |
specific reaction | 10 |
reliable detection | 10 |
clinical management | 10 |
gene rt | 10 |
qiaamp viral | 10 |
quantitative detection | 10 |
novel sars | 10 |
study showed | 10 |
methods require | 10 |
gene primers | 10 |
dna sequencing | 10 |
time consuming | 10 |
lamp may | 10 |
reaction system | 10 |
virus dna | 10 |
rna amplification | 10 |
detection rates | 10 |
healthy individuals | 10 |
assay detected | 10 |
amplification reactions | 10 |
molecular techniques | 10 |
human coronavirus | 10 |
hcr reaction | 10 |
ulcerans infection | 10 |
infectious agents | 10 |
nervous system | 10 |
template rna | 10 |
wide range | 10 |
simple method | 10 |
lamp technique | 10 |
pcr using | 10 |
classical swine | 10 |
enterotoxigenic escherichia | 10 |
colour change | 10 |
positive predictive | 10 |
quantitative real | 10 |
two samples | 10 |
blue dye | 10 |
molecular test | 10 |
positive rt | 10 |
wild type | 10 |
ec nv | 10 |
akt mtor | 10 |
buccal swab | 10 |
rna per | 10 |
two sets | 10 |
independent cohort | 10 |
dna strand | 10 |
danon disease | 10 |
structural proteins | 10 |
aldh glu | 10 |
two methods | 10 |
different concentrations | 10 |
forward primer | 10 |
asian genotype | 10 |
novel reverse | 10 |
using rna | 10 |
amplification development | 10 |
growth factor | 10 |
inhibit autophagy | 10 |
pulmonary adenocarcinoma | 10 |
human respiratory | 10 |
molecular weight | 10 |
autophagy autophagy | 10 |
fip bip | 10 |
tris buffer | 10 |
likelihood ratios | 10 |
methods doi | 10 |
septicaemia virus | 10 |
samples containing | 10 |
optigene ltd | 10 |
early stages | 9 |
open access | 9 |
warmstart colorimetric | 9 |
multiplex rt | 9 |
amplification product | 9 |
minor gii | 9 |
epithelial cells | 9 |
field conditions | 9 |
recognize six | 9 |
zoster virus | 9 |
pcr tests | 9 |
different primer | 9 |
care test | 9 |
realtime pcr | 9 |
optimal temperature | 9 |
chronic hepatitis | 9 |
sample type | 9 |
single nucleotide | 9 |
without dna | 9 |
ph indicator | 9 |
prevalent gii | 9 |
commercial kit | 9 |
purified using | 9 |
high risk | 9 |
patients infected | 9 |
untranslated region | 9 |
stem cell | 9 |
coronavirus infection | 9 |
rdrp gene | 9 |
extraction kits | 9 |
direct amplification | 9 |
small molecule | 9 |
scale testing | 9 |
chik infection | 9 |
class ii | 9 |
template control | 9 |
chest ct | 9 |
microfluidic chip | 9 |
rapid test | 9 |
detection assay | 9 |
reaction solution | 9 |
staphylococcus aureus | 9 |
flow assay | 9 |
iron homeostasis | 9 |
qpcr test | 9 |
respiratory samples | 9 |
tumor progression | 9 |
high throughput | 9 |
effective diagnostic | 9 |
pcv lamp | 9 |
time turbidimeter | 9 |
lower sensitivity | 9 |
care home | 9 |
molecular tests | 9 |
using two | 9 |
eight distinct | 9 |
alere i | 9 |
confirmed cases | 9 |
life technologies | 9 |
antiviral drugs | 9 |
ns gene | 9 |
amplification date | 9 |
quantifi cation | 9 |
target nucleic | 9 |
clinical evaluation | 9 |
purified rna | 9 |
target amplification | 9 |
open reading | 9 |
well plates | 9 |
situ hybridization | 9 |
based assay | 9 |
bst polymerase | 9 |
pot real | 9 |
confidence interval | 9 |
potential use | 9 |
pcr machine | 9 |
oropharyngeal swab | 9 |
viral antigens | 9 |
extraction step | 9 |
using isothermal | 9 |
cdc real | 9 |
case report | 9 |
intercalating dyes | 9 |
stroke treatment | 9 |
measured using | 9 |
polymerase promoter | 9 |
infected samples | 9 |
primary material | 9 |
rna fragment | 9 |
novel nucleic | 9 |
overall sensitivity | 9 |
emerging viruses | 9 |
qpcr results | 9 |
trained personnel | 9 |
nucleotide polymorphisms | 9 |
human influenza | 9 |
detection unit | 9 |
respiratory specimens | 9 |
er stress | 9 |
mm edta | 9 |
mm mgcl | 9 |
artery stenting | 9 |
powdery mildew | 9 |
enzyme mix | 9 |
recent advances | 9 |
asymptomatic carrier | 9 |
times higher | 9 |
amplification combined | 9 |
expensive instrumentation | 9 |
polymerase gene | 9 |
gmo detection | 9 |
melt curve | 9 |
control group | 9 |
cmnv rt | 9 |
specifically designed | 9 |
recent years | 9 |
conventional kit | 9 |
creative commons | 9 |
new coronavirus | 9 |
serum specimens | 9 |
dna development | 9 |
viral sequences | 9 |
loop dna | 9 |
allantoic fluid | 9 |
cavity effusions | 9 |
global pandemic | 9 |
autophagy may | 9 |
sequence based | 8 |
white precipitate | 8 |
protein gene | 8 |
using colorimetric | 8 |
nucleocapsid protein | 8 |
gene specific | 8 |
innate immune | 8 |
ha gene | 8 |
lamp showed | 8 |
field detection | 8 |
amv reverse | 8 |
converting enzyme | 8 |
lamp methods | 8 |
genefinder tm | 8 |
may also | 8 |
loop structure | 8 |
conserved regions | 8 |
pcr inhibitors | 8 |
processing time | 8 |
recent outbreak | 8 |
acute ischemic | 8 |
experimentally infected | 8 |
cellular autophagy | 8 |
amplification loop | 8 |
ml reaction | 8 |
cell survival | 8 |
inverted repeats | 8 |
internal primers | 8 |
testing methods | 8 |
nonspecific amplification | 8 |
light source | 8 |
including two | 8 |
target genes | 8 |
supplementary material | 8 |
using ph | 8 |
detection platform | 8 |
method using | 8 |
optimized rt | 8 |
stem loop | 8 |
tissue kit | 8 |
positive rate | 8 |
lamp pcr | 8 |
reference laboratory | 8 |
study design | 8 |
cation method | 8 |
acute gastroenteritis | 8 |
fully automated | 8 |
zikv infection | 8 |
supporting information | 8 |
amplification system | 8 |
cohort study | 8 |
fi gure | 8 |
traditional chinese | 8 |
time assays | 8 |
cell surface | 8 |
without loop | 8 |
primer combinations | 8 |
based diagnostics | 8 |
endoplasmic reticulum | 8 |
transcription loopmediated | 8 |
correlation coefficient | 8 |
methods used | 8 |
dna strands | 8 |
grape powdery | 8 |
kidney disease | 8 |
hais due | 8 |
reaction units | 8 |
assay results | 8 |
early stage | 8 |
primer specificity | 8 |
several studies | 8 |
erysiphe necator | 8 |
reaction unit | 8 |
sets targeting | 8 |
infl uenza | 8 |
based testing | 8 |
reverse primer | 8 |
beclin expression | 8 |
forward loop | 8 |
aichi virus | 8 |
signal amplification | 8 |
stem cells | 8 |
routine rt | 8 |
sequence alignment | 8 |
based real | 8 |
data analysis | 8 |
infected cells | 8 |
mean detection | 8 |
signaling pathways | 8 |
primers fip | 8 |
hda system | 8 |
denv rt | 8 |
lamp testing | 8 |
test kits | 8 |
atg expression | 8 |
large fragment | 8 |
viral transport | 8 |
amplification technology | 8 |
clinical features | 8 |
developed using | 8 |
time nucleic | 8 |
dependent isothermal | 8 |
cell line | 8 |
turbidity detection | 8 |
detection techniques | 8 |
immune responses | 8 |
reaction chamber | 8 |
initial denaturation | 8 |
suspected patients | 8 |
rna sequences | 8 |
disease caused | 8 |
microfluidic devices | 8 |
easy detection | 8 |
dna polymerases | 8 |
amplified using | 8 |
coronavirus rna | 8 |
simple detection | 8 |
cohort ii | 8 |
i influenza | 8 |
step reverse | 8 |
pregnant women | 8 |
optimized lamp | 8 |
direct nucleic | 8 |
first report | 8 |
cell lines | 8 |
designed based | 8 |
hemagglutinin gene | 8 |
evaluated using | 8 |
single stranded | 8 |
ndv strains | 8 |
fip primers | 8 |
agarose beads | 8 |
mouse model | 8 |
pcr based | 8 |
smartphone camera | 8 |
roundup ready | 8 |
nv detection | 8 |
specific real | 8 |
global health | 8 |
time point | 7 |
fluorescence intensity | 7 |
mineral oil | 7 |
multiplexed rt | 7 |
target snp | 7 |
genomic rna | 7 |
two additional | 7 |
time lamp | 7 |
pcr cycler | 7 |
protein aggregates | 7 |
institutional review | 7 |
automated microfluidic | 7 |
set targeting | 7 |
positive amplification | 7 |
san diego | 7 |
valproic acid | 7 |
minimum concentration | 7 |
genomic sequences | 7 |
severe cases | 7 |
pcr reactions | 7 |
plasmon resonance | 7 |
id now | 7 |
pot visual | 7 |
autophagy research | 7 |
nv gi | 7 |
sample rods | 7 |
science foundation | 7 |
qpcr kit | 7 |
genome amplification | 7 |
diagnostic sensitivity | 7 |
assay targeting | 7 |
diagnosis using | 7 |
accurate diagnostic | 7 |
spore samplers | 7 |
rapid rt | 7 |
previously reported | 7 |
base pairs | 7 |
lamp master | 7 |
duck hepatitis | 7 |
plasmid standards | 7 |
enzymatic amplification | 7 |
specific primer | 7 |
excessive autophagy | 7 |
transport medium | 7 |
two major | 7 |
accelerating primer | 7 |
blood sample | 7 |
mhc class | 7 |
binding protein | 7 |
diagnostic tools | 7 |
template input | 7 |
serological assays | 7 |
plasmid dna | 7 |
serial diluted | 7 |
stepone tm | 7 |
greater sensitivity | 7 |
final extension | 7 |
reverse primers | 7 |
bronchoalveolar lavage | 7 |
based rna | 7 |
extremely high | 7 |
emerging infectious | 7 |
isothermal condition | 7 |
microfluidic device | 7 |
taq polymerase | 7 |
human cells | 7 |
white spot | 7 |
molecular beacons | 7 |
penaeus monodon | 7 |
recently developed | 7 |
detection based | 7 |
lamp amplifi | 7 |
autophagy inhibition | 7 |
sample size | 7 |
fold dilutions | 7 |
lamp result | 7 |
standard rt | 7 |
four sets | 7 |
final concentration | 7 |
north america | 7 |
related viruses | 7 |
high viral | 7 |
rna target | 7 |
polymerase used | 7 |
online version | 7 |
transcriptase loop | 7 |
dna helicase | 7 |
rna fragments | 7 |
samples isolated | 7 |
herpesvirus dna | 7 |
containing ml | 7 |
asymptomatic carriers | 7 |
centrifugal platform | 7 |
autophagy induction | 7 |
denv serotypes | 7 |
mortality disease | 7 |
molecular beacon | 7 |
detection kit | 7 |
virus loop | 7 |
mixture contained | 7 |
negative reactions | 7 |
poc test | 7 |
respiratory disease | 7 |
neisseria gonorrhoeae | 7 |
routine clinical | 7 |
prevent cross | 7 |
specialized equipment | 7 |
based lamp | 7 |
diagnostic platform | 7 |
qiacube extraction | 7 |
sense sequence | 7 |
cost effectiveness | 7 |
test using | 7 |
lamp mixture | 7 |
clinical setting | 7 |
established rt | 7 |
gene fragment | 7 |
camostat mesylate | 7 |
positive clinical | 7 |
analyzed using | 7 |
automated centrifugal | 7 |
subsequent amplification | 7 |
ibv strains | 7 |
clostridium difficile | 7 |
diagnostic potential | 7 |
min using | 7 |
denv ns | 7 |
successfully applied | 7 |
zikv strains | 7 |
lamp target | 7 |
monocytogenes dna | 7 |
coat protein | 7 |
hemorrhagic fever | 7 |
temperature range | 7 |
autophagy protein | 7 |
transcription pcr | 7 |
virus strains | 7 |
require expensive | 7 |
primer regions | 7 |
capsid protein | 7 |
membrane protein | 7 |
biological substances | 7 |
specifi city | 7 |
bacterial infection | 7 |
coronavirus rapid | 7 |
chamber i | 7 |
dna templates | 7 |
reaction denv | 7 |
innate immunity | 7 |
pcr analysis | 7 |
low cost | 7 |
review board | 7 |
specific loop | 7 |
small sample | 7 |
spore quantities | 7 |
high numbers | 7 |
electron microscopy | 7 |
growing season | 7 |
defective autophagy | 7 |
white shrimp | 7 |
ncov infection | 7 |
gene copy | 7 |
innovative gene | 7 |
examined using | 7 |
high degree | 7 |
autoimmune diseases | 7 |
viral particles | 7 |
cell lysis | 7 |
true positive | 7 |
specimens collected | 7 |
direct rt | 7 |
integrated microfluidic | 7 |
hepatocellular carcinoma | 7 |
like structures | 7 |
negative diagnosis | 7 |
fluorescent detection | 7 |
taqman real | 7 |
simple operation | 7 |
nasopharyngeal specimens | 7 |
hot swab | 7 |
accurate diagnosis | 7 |
two cohorts | 7 |
poc applications | 7 |
primer pairs | 7 |
mutation detection | 7 |
heidelberg university | 7 |
low concentrations | 7 |
patient sample | 7 |
diagnostic qpcr | 7 |
antibody responses | 7 |
also used | 7 |
detect rna | 7 |
ns rt | 7 |
novel method | 7 |
extraction using | 7 |
stool samples | 7 |
virus isolates | 7 |
care settings | 7 |
reactions using | 7 |
lamp using | 7 |
dna extracted | 7 |
signaling pathway | 7 |
analysis using | 7 |
direct testing | 7 |
acute stage | 7 |
gargle lavages | 7 |
confirmed covid | 7 |
lamp mix | 7 |
negative rt | 7 |
following intravenous | 7 |
double stranded | 7 |
matrix gene | 7 |
assay rapid | 7 |
oilseed rape | 7 |
scored negative | 7 |
surface plasmon | 7 |
vp gene | 7 |
showed high | 7 |
reagent injection | 7 |
two pairs | 7 |
snps detection | 7 |
sensitive dyes | 7 |
written informed | 7 |
time nasba | 7 |
commercial kits | 7 |
amino acid | 7 |
ccc pipeline | 7 |
detected using | 7 |
proliferative kidney | 7 |
dna accelerated | 7 |
signal enhancement | 6 |
complementary strand | 6 |
free molecular | 6 |
rapid method | 6 |
pipette tips | 6 |
chinese medicine | 6 |
control line | 6 |
one single | 6 |
genetic variation | 6 |
nm annealed | 6 |
personalized medicine | 6 |
clinical study | 6 |
molecular characterization | 6 |
large amount | 6 |
directly added | 6 |
respiratory viral | 6 |
per sample | 6 |
avian myeloblastosis | 6 |
crispr diagnostics | 6 |
patient management | 6 |
screening method | 6 |
calculated using | 6 |
simulation samples | 6 |
ge gene | 6 |
fecal specimens | 6 |
negative patients | 6 |
rapid reaction | 6 |
products using | 6 |
least one | 6 |
turbidity assay | 6 |
like bands | 6 |
inhibits autophagy | 6 |
transcription step | 6 |
mm thick | 6 |
one hour | 6 |
synthetic sars | 6 |
denv rna | 6 |
software program | 6 |
speed centrifugation | 6 |
target rt | 6 |
alternately inverted | 6 |
amplify dna | 6 |
plasmodium falciparum | 6 |
abbott id | 6 |
broad range | 6 |
per ml | 6 |
based signal | 6 |
spot syndrome | 6 |
mm kcl | 6 |
unfolded protein | 6 |
different primers | 6 |
using fluorescent | 6 |
pacific white | 6 |
porcine circoviruses | 6 |
antigen presentation | 6 |
amplification times | 6 |
different temperatures | 6 |
membrane fusion | 6 |
high consistency | 6 |
background dna | 6 |
rna sequence | 6 |
primers specific | 6 |
serological methods | 6 |
protein response | 6 |
lamp amplified | 6 |
primer designing | 6 |
molecular mechanisms | 6 |
dengue infection | 6 |
one study | 6 |
life sciences | 6 |
takes place | 6 |
showed higher | 6 |
tm system | 6 |
water samples | 6 |
isothermal detection | 6 |
new method | 6 |
amplification speed | 6 |
poor settings | 6 |
ndv alone | 6 |
amplification step | 6 |
cdna synthesis | 6 |
independent sequences | 6 |
oncorhynchus mykiss | 6 |
autophagy via | 6 |
pvx rna | 6 |
time polymerase | 6 |
rapid screening | 6 |
autophagy inhibitors | 6 |
regulate autophagy | 6 |
zikv sequences | 6 |
diagnostic performance | 6 |
quantitative results | 6 |
tested negative | 6 |
papillomavirus type | 6 |
six different | 6 |
determined using | 6 |
detected within | 6 |
fluorescence signals | 6 |
sensitivity compared | 6 |
table iv | 6 |
infected pigs | 6 |
cell growth | 6 |
multiple displacement | 6 |
lamp devices | 6 |
important role | 6 |
backward outer | 6 |
commercial rna | 6 |
natural science | 6 |
respiratory pathogens | 6 |
blood plasma | 6 |
lamp approach | 6 |
pyrophosphate ions | 6 |
valuable tool | 6 |
internal carotid | 6 |
using crispr | 6 |
medical sciences | 6 |
loop dnas | 6 |
dna samples | 6 |
based method | 6 |
since lamp | 6 |
rna kit | 6 |
similar sensitivity | 6 |
avian infectious | 6 |
autophagic degradation | 6 |
also performed | 6 |
food samples | 6 |
biosafety level | 6 |
generated using | 6 |
human blood | 6 |
randomly selected | 6 |
purification step | 6 |
northwest university | 6 |
ndv detection | 6 |
respiratory infections | 6 |
coronavirus pneumonia | 6 |
forming units | 6 |
homozygous mutation | 6 |
promoter sequence | 6 |
dao thi | 6 |
accession numbers | 6 |
extremely useful | 6 |
gel stained | 6 |
clinical trial | 6 |
diabetes mellitus | 6 |
single rt | 6 |
cervical cancer | 6 |
slit lamp | 6 |
commercial isothermal | 6 |
bowenoid papulosis | 6 |
standard method | 6 |
reading frame | 6 |
mycoplasma pneumoniae | 6 |
denv serotype | 6 |
min time | 6 |
protein kinase | 6 |
standard operating | 6 |
provide appropriate | 6 |
ncov detection | 6 |
complementary dna | 6 |
pandemic influenza | 6 |
culture medium | 6 |
critical review | 6 |
sample handling | 6 |
traditional pcr | 6 |
dna sequence | 6 |
necator dna | 6 |
small cell | 6 |
breast cancer | 6 |
viruses including | 6 |
amplification results | 6 |
novel anti | 6 |
autophagic cell | 6 |
tumor cell | 6 |
dnase rnase | 6 |
specificity study | 6 |
increase sensitivity | 6 |
assay demonstrated | 6 |
successfully detected | 6 |
multiple loops | 6 |
health emergency | 6 |
viruses using | 6 |
detecting pedv | 6 |
first time | 6 |
west sussex | 6 |
endemic countries | 6 |
two hospitals | 6 |
different genotypes | 6 |
molecular biology | 6 |
like viruses | 6 |
lamp shield | 6 |
without fip | 6 |
mortality rate | 6 |
ivt rna | 6 |
digital droplet | 6 |
ex taq | 6 |
also showed | 6 |
fold dilution | 6 |
uorescent dye | 6 |
table i | 6 |
probe sets | 6 |
immune cells | 6 |
answer detection | 6 |
displacement reaction | 6 |
kinase complex | 6 |
vitro transcription | 6 |
complete genome | 6 |
south america | 6 |
customized instrument | 6 |
pcr positive | 6 |
volume containing | 6 |
care diagnostic | 6 |
melting temperature | 6 |
myeloblastosis virus | 6 |
method may | 6 |
commons attribution | 6 |
infected fish | 6 |
phosphate buffered | 6 |
similar results | 6 |
fine needle | 6 |
blot hybridization | 6 |
nonstructural proteins | 6 |
microbial infections | 6 |
mononuclear cells | 6 |
rna genome | 6 |
infected bhk | 6 |
fluorescence microscopy | 6 |
laboratory confirmation | 6 |
four samples | 6 |
mtor pathway | 6 |
ml eppendorf | 6 |
sensitive loop | 6 |
regulates autophagy | 6 |
southeast asia | 6 |
likelihood ratio | 6 |
early detection | 6 |
rna mini | 6 |
field applications | 6 |
animal health | 6 |
lamp detected | 6 |
gene expression | 6 |
helicase dependent | 6 |
simple water | 6 |
i dye | 6 |
also developed | 6 |
measles virus | 6 |
cerebrospinal fluid | 6 |
genie ii | 6 |
heat treatment | 6 |
targeting orf | 6 |
ndv rna | 6 |
dna extractions | 6 |
clinical laboratories | 6 |
genotype sequences | 6 |
respiratory secretions | 6 |
melting curve | 6 |
mediated detection | 6 |
chinese academy | 6 |
standard deviation | 6 |
review editing | 6 |
loop structures | 6 |
gii primer | 6 |
assay system | 6 |
loops formed | 6 |
cancer therapy | 6 |
genital lesions | 6 |
ap pathway | 6 |
previous reports | 6 |
plasma samples | 6 |
dna polymerization | 6 |
dna directly | 6 |
using molecular | 6 |
target region | 6 |
patients suspected | 6 |
virus development | 6 |
using dna | 6 |
inhibitory effect | 6 |
sangon biotech | 6 |
isothermal techniques | 6 |
based dlamp | 6 |
inoculum detection | 6 |
asymptomatic covid | 6 |
effective method | 6 |
isothermal amplificatio | 6 |
eppendorf tube | 6 |
magnetic rack | 6 |
starting structure | 6 |
metal block | 6 |
blood mononuclear | 6 |
yellow fever | 6 |
strains used | 6 |
guanidine hydrochloride | 6 |
tertiary care | 6 |
integrated dna | 6 |
lavage fluid | 6 |
clinical practice | 6 |
poc testing | 6 |
temperature cycling | 5 |
dis doi | 5 |
amplify target | 5 |
gp helicase | 5 |
coronavirus loop | 5 |
three primer | 5 |
bovine serum | 5 |
may improve | 5 |
crude dna | 5 |
simple isothermal | 5 |
significant difference | 5 |
ngs confirmation | 5 |
overall specificity | 5 |
lupus erythematosus | 5 |
quantified using | 5 |
incubation time | 5 |
green color | 5 |
quantitative assay | 5 |
operating procedures | 5 |
virus infections | 5 |
related protein | 5 |
supplementary data | 5 |
multiplex loop | 5 |
products showed | 5 |
control template | 5 |
valley fever | 5 |
chikungunya fever | 5 |
close contact | 5 |
way junction | 5 |
major advantage | 5 |
targeting severe | 5 |
molecular size | 5 |
health care | 5 |
time turbidimetry | 5 |
high ct | 5 |
rapid amplification | 5 |
biotech co | 5 |
displacing polymerase | 5 |
min incubation | 5 |
portable device | 5 |
tumor suppression | 5 |
pcr testing | 5 |
accessory proteins | 5 |
selected based | 5 |
via autophagy | 5 |
field use | 5 |
promising approach | 5 |
phase serum | 5 |
tube rt | 5 |
dna ladder | 5 |
heart failure | 5 |
amplify specific | 5 |
drug administration | 5 |
seed plate | 5 |
clinical serum | 5 |
inconsistent results | 5 |
small amount | 5 |
assay used | 5 |
newly designed | 5 |
nested polymerase | 5 |
rapid early | 5 |
commercial qiacube | 5 |
receptor binding | 5 |
assays performed | 5 |
complex samples | 5 |
strand displacing | 5 |
centrifugal force | 5 |
using serial | 5 |
true negative | 5 |
autophagy proteins | 5 |
detection process | 5 |
specifically amplify | 5 |
acid purification | 5 |
dna replication | 5 |
hae iii | 5 |
gastroenteritis virus | 5 |
situ reverse | 5 |
plasmids containing | 5 |
sputum specimens | 5 |
based test | 5 |
one primer | 5 |
clinical manifestations | 5 |
ms rf | 5 |
hbv viral | 5 |
central nervous | 5 |
target concentrations | 5 |
genotype zikv | 5 |
rnase free | 5 |
autophagy plays | 5 |
flow icts | 5 |
personal protective | 5 |
dna intermediate | 5 |
leafroll virus | 5 |
monoclonal antibodies | 5 |
amino acids | 5 |
green fluorescence | 5 |
confirmed using | 5 |
national institute | 5 |
reported previously | 5 |
higher amplification | 5 |
routine diagnostic | 5 |
molecular grade | 5 |
sequence replication | 5 |
tubes containing | 5 |
sequence complementary | 5 |
care homes | 5 |
protective equipment | 5 |
low positive | 5 |
widely available | 5 |
dna real | 5 |
positive patients | 5 |
acs synthetic | 5 |
transcriptase step | 5 |
rotation rate | 5 |
detection tool | 5 |
multiplex tandem | 5 |
supplementary information | 5 |
monitoring methods | 5 |
designed targeting | 5 |
autophagy regulation | 5 |
gg gene | 5 |
tgev detection | 5 |
dry swabs | 5 |
chamber ii | 5 |
observational cohort | 5 |
relatively low | 5 |
qpcr testing | 5 |
protease inhibitor | 5 |
tumor suppressor | 5 |
us government | 5 |
detection reagent | 5 |
lamp process | 5 |
diagnostics using | 5 |
vitro antiviral | 5 |
surplus material | 5 |
field samples | 5 |
lamp also | 5 |
lysosomal dysfunction | 5 |
stem lengths | 5 |
uv illumination | 5 |
samples also | 5 |
quantifying template | 5 |
visual observation | 5 |
ill patients | 5 |
infectious hematopoietic | 5 |
determine whether | 5 |
coli uvrd | 5 |
turbidity measurement | 5 |
org synthbio | 5 |
nan doi | 5 |
deletion mutation | 5 |
virol doi | 5 |
mosaic virus | 5 |
throat swabs | 5 |
increased sensitivity | 5 |
reference strains | 5 |
recently reported | 5 |
fluorescent signal | 5 |
infected culture | 5 |
cell cycle | 5 |
gene primer | 5 |
transcription recombinase | 5 |
alternative method | 5 |
diagnostic laboratories | 5 |
warmstart dna | 5 |
signal magnitude | 5 |
displacing dna | 5 |
molecular testing | 5 |
based rt | 5 |
lamp procedure | 5 |
autophagosome maturation | 5 |
nondenatured template | 5 |
mbs bio | 5 |
samples rapid | 5 |
performed without | 5 |
specific regions | 5 |
access article | 5 |
listeria species | 5 |
optimized conditions | 5 |
synthetic rna | 5 |
grand island | 5 |
low concentration | 5 |
assimilating probe | 5 |
care nucleic | 5 |
nbnm beads | 5 |
systematic review | 5 |
major role | 5 |
step amplification | 5 |
point mutations | 5 |
human fecal | 5 |
pyrophosphate precipitate | 5 |
sample pre | 5 |
hmg box | 5 |
disease detection | 5 |
hs bp | 5 |
field application | 5 |
reaction product | 5 |
biotechnology co | 5 |
laboratory testing | 5 |
potato virus | 5 |
based dna | 5 |
autocycling strand | 5 |
typically used | 5 |
enzyme linked | 5 |
reaction efficiency | 5 |
likely due | 5 |
orange color | 5 |
disease severity | 5 |
chemical reaction | 5 |
cells autophagy | 5 |
reference rt | 5 |
transcription lamp | 5 |
amplification real | 5 |
available online | 5 |
autophagy machinery | 5 |
common respiratory | 5 |
global public | 5 |
standard procedures | 5 |
strains isolated | 5 |
detection strategy | 5 |
gene protein | 5 |
utm pbs | 5 |
electrochemical detection | 5 |
result diagnosis | 5 |
southern india | 5 |
ulcerans disease | 5 |
mixture containing | 5 |
diagnostic technique | 5 |
two separate | 5 |
rna directly | 5 |
assays require | 5 |
porcine viruses | 5 |
strand exchange | 5 |
min followed | 5 |
input volume | 5 |
test line | 5 |
nucleotide database | 5 |
direct swab | 5 |
article distributed | 5 |
identifi cation | 5 |
condyloma acuminatum | 5 |
sense rna | 5 |
related genes | 5 |
human genome | 5 |
detected vhs | 5 |
multiplex real | 5 |
forward outer | 5 |
mammalian autophagy | 5 |
even higher | 5 |
rift valley | 5 |
genome sequence | 5 |
positive lamp | 5 |
antiplatelet medication | 5 |
cation methods | 5 |
transcriptional loop | 5 |
acute denv | 5 |
bacterial pathogens | 5 |
potato viruses | 5 |
naoh solution | 5 |
molecular method | 5 |
potato leafroll | 5 |
primer fip | 5 |
vhs serotypes | 5 |
control reactions | 5 |
also observed | 5 |
future perspectives | 5 |
systemic lupus | 5 |
temple johnson | 5 |
directly without | 5 |
designed primer | 5 |
hcv infection | 5 |
direct visualization | 5 |
fold greater | 5 |
one microliter | 5 |
genotyping results | 5 |
gene based | 5 |
aichi viruses | 5 |
six regions | 5 |
ic ct | 5 |
positive test | 5 |
reverse transcriptional | 5 |
negative regulator | 5 |
disease progression | 5 |
used method | 5 |
results demonstrated | 5 |
gi primer | 5 |
hematopoietic necrosis | 5 |
zikv strain | 5 |
international concern | 5 |
useful tool | 5 |
primers within | 5 |
inconsistent samples | 5 |
conditions using | 5 |
correctly identified | 5 |
lamp kit | 5 |
clinical utility | 5 |
may provide | 5 |
sherlock assays | 5 |
qiacube rna | 5 |
explorer version | 5 |
imaging system | 5 |
loopamp real | 5 |
potential therapeutic | 5 |
ct imaging | 5 |
taqman probes | 5 |
differential diagnosis | 5 |
mathematical model | 5 |
african trypanosomes | 5 |
care detection | 5 |
computed tomography | 5 |
polymerase inhibitors | 5 |
colon cancer | 5 |
leaf curl | 5 |
high correlation | 5 |
detect ibv | 5 |
method used | 5 |
control measures | 5 |
swabs without | 5 |
different types | 5 |
dye sybr | 5 |
high efficiency | 5 |
quantitative analysis | 5 |
therapeutic target | 5 |
ppv vp | 5 |
see table | 5 |
selected temperature | 5 |
shellfish diseases | 5 |
positive cases | 5 |
spurious amplification | 5 |
reaction condition | 5 |
cardiovascular diseases | 5 |
positive using | 5 |
may cause | 5 |
porcine pegivirus | 5 |
detect human | 5 |
research institute | 5 |
transcriptase pcr | 5 |
amplification directly | 5 |
new approach | 5 |
viruses detection | 5 |
sample nucleic | 5 |
clinical specimen | 5 |
detect ppv | 5 |
ml total | 5 |
promote cell | 5 |
later stages | 5 |
dna technologies | 5 |
tract infections | 5 |
induced apoptosis | 5 |
acid release | 5 |
samples positive | 5 |
monoclonal antibody | 5 |
noise ratio | 5 |
amies medium | 5 |
rna concentration | 5 |
results show | 5 |
better sensitivity | 5 |
novel dna | 5 |
higher sensitivities | 5 |
negative likelihood | 5 |
potential cross | 5 |
samples diluted | 5 |
coronavirus severe | 5 |
isolation kit | 5 |
diluted sybr | 5 |
biology pubs | 5 |
kindly provided | 5 |
genbank database | 5 |
data curation | 5 |
order nidovirales | 5 |
egfr pcr | 5 |
mesenchymal stem | 5 |
small amounts | 5 |
coronavirus associated | 5 |
sample matrix | 5 |
scientific research | 5 |
gradient pcr | 5 |
reference genome | 5 |
large number | 5 |
cold metal | 5 |
heat inactivation | 5 |
four different | 5 |
primer pair | 5 |
one sample | 5 |
rna technology | 5 |
qlamp detection | 5 |
exact test | 5 |
autophagosome biogenesis | 5 |
ph value | 5 |
ml lamp | 5 |
rpa reaction | 5 |
rna standards | 5 |
pcr primers | 5 |
hcr products | 5 |
tissue culture | 5 |
dna using | 5 |
detecting viral | 5 |
needle aspirates | 5 |
human monoclonal | 5 |
nicking enzyme | 5 |
channel layer | 5 |
positive sample | 5 |
per well | 5 |
financial support | 5 |
buffered saline | 5 |
additional primers | 5 |
threshold time | 5 |
step process | 5 |
specificity test | 5 |
etiological agent | 5 |
future studies | 5 |
annealing temperature | 5 |
significant number | 5 |
approximately min | 5 |
fatal disease | 5 |
associated protein | 5 |
uv lamp | 5 |
community settings | 5 |
visualized via | 5 |
rna transcripts | 5 |
ndv templates | 5 |
specific reactions | 5 |
spin column | 5 |
comparable sensitivity | 5 |
therascreen egfr | 5 |
sensitive method | 5 |
high mortality | 5 |
funding acquisition | 5 |
highly desirable | 5 |
equipped laboratories | 5 |
arbovirus infection | 5 |
also applied | 5 |
ulk complex | 5 |
droplet pcr | 5 |
software primer | 5 |
nasba assay | 5 |
annealing temperatures | 5 |
microfluidic chips | 5 |
lyophilized reagents | 5 |
viral detection | 5 |
blast search | 5 |
throughput sequencing | 5 |
viral diagnostics | 5 |
sensitivity using | 5 |
signal change | 5 |
observed directly | 5 |
therascreen assay | 5 |
indian ocean | 5 |
stock solution | 5 |
virus titer | 5 |
reticulum stress | 5 |
clinical laboratory | 5 |
tn transposase | 5 |
diagnostic applications | 5 |
cell development | 5 |
single infected | 5 |
national science | 5 |
dna damage | 5 |
hda systems | 5 |
samples used | 5 |
curl virus | 5 |
table shows | 5 |
synthetic biology | 5 |
requires expensive | 5 |
dna molecular | 5 |
warmer lamp | 5 |
ml buffer | 5 |
autophagy pathway | 5 |
synthbio review | 5 |
visualized directly | 4 |
envelope protein | 4 |
size marker | 4 |
frequently used | 4 |
similar viruses | 4 |
interacting protein | 4 |
circulating strains | 4 |
continuous flow | 4 |
designed set | 4 |
background interference | 4 |
prm gene | 4 |
genetic testing | 4 |
low copy | 4 |
amplification helicase | 4 |
also thank | 4 |
salmonella typhimurium | 4 |
current knowledge | 4 |
health systems | 4 |
patient nasopharyngeal | 4 |
also detected | 4 |
viral burden | 4 |
may require | 4 |
repeated testing | 4 |
detection procedure | 4 |
nasopharyngeal samples | 4 |
viral protein | 4 |
early phase | 4 |
primer binds | 4 |
hereditary spastic | 4 |
also included | 4 |
may occur | 4 |
primers hybridize | 4 |
active form | 4 |
genomic sequence | 4 |
lysosomal proteases | 4 |
cycle progression | 4 |
synthesized dna | 4 |
significantly higher | 4 |
colorimetric readout | 4 |
disposable pocket | 4 |
reactive oxygen | 4 |
japanese yam | 4 |
spiral chip | 4 |
chicken embryos | 4 |
southern blot | 4 |
several intrinsic | 4 |
samples directly | 4 |
family coronaviridae | 4 |
eid ml | 4 |
supplemental material | 4 |
dual role | 4 |
based extraction | 4 |
avian virus | 4 |
pcr without | 4 |
expensive instruments | 4 |
well pcr | 4 |
either high | 4 |
necator conidia | 4 |
active covid | 4 |
class i | 4 |
target regions | 4 |
also reported | 4 |
like illness | 4 |
mtor signaling | 4 |
flow cabinet | 4 |
conducted qlamp | 4 |
colorectal cancer | 4 |
strand invasion | 4 |
often cumbersome | 4 |
using isolated | 4 |
preliminary results | 4 |
high pure | 4 |
exhibit increased | 4 |
laboratory tests | 4 |
surveillance studies | 4 |
based nucleic | 4 |
shenzhen luohu | 4 |
diagnostic rt | 4 |
cell membrane | 4 |
chip release | 4 |
identify infected | 4 |
laser diode | 4 |
virus stock | 4 |
corresponding author | 4 |
ppgv infection | 4 |
recognize eight | 4 |
identical reaction | 4 |
reported lamp | 4 |
lamp developed | 4 |
health concern | 4 |
single test | 4 |
virus disease | 4 |
chinese center | 4 |
three major | 4 |
step single | 4 |
kisker biotech | 4 |
cellular entry | 4 |
set used | 4 |
may serve | 4 |
tm ii | 4 |
respiratory distress | 4 |
transcription factors | 4 |
side effects | 4 |
drug metabolism | 4 |
amplifi ed | 4 |
lower concentration | 4 |
eukaryotic initiation | 4 |
sample volume | 4 |
dendritic cells | 4 |
sensitive reverse | 4 |
lamp employs | 4 |
bubble plots | 4 |
definitive diagnosis | 4 |
important lessons | 4 |
repurposed drugs | 4 |
using uv | 4 |
plays important | 4 |
heat transfer | 4 |
cell therapy | 4 |
heating module | 4 |
relatively conserved | 4 |
pcr detected | 4 |
inactivated nasopharyngeal | 4 |
sequencing run | 4 |
cap gene | 4 |
bowel disease | 4 |
regulated optical | 4 |
daan gene | 4 |
lysosomal membrane | 4 |
loopamp rna | 4 |
qpcr machine | 4 |
detect target | 4 |
polymerase large | 4 |
cmnv plasmid | 4 |
taq tm | 4 |
sample treatment | 4 |
autophagy deficiency | 4 |
dna target | 4 |
fold serially | 4 |
technology co | 4 |
validated using | 4 |
various concentrations | 4 |
air samples | 4 |
carryover contamination | 4 |
least times | 4 |
two negative | 4 |
care hospital | 4 |
tetracapsuloides bryosalmonae | 4 |
clinical characteristics | 4 |
autophagy enhancer | 4 |
rural areas | 4 |
scored positive | 4 |
gene segments | 4 |
classical lamp | 4 |
touchdown pcr | 4 |
autophagy stimulation | 4 |
circulating nucleic | 4 |
obtained within | 4 |
tests using | 4 |
hairpin assembly | 4 |
rheumatoid arthritis | 4 |
small round | 4 |
iii reverse | 4 |
whole genome | 4 |
sealing layer | 4 |
autophagy protects | 4 |
designed four | 4 |
within one | 4 |
symptomatic patients | 4 |
detecting hcv | 4 |
biomedical importance | 4 |
stimulate autophagy | 4 |
beclin overexpression | 4 |
using different | 4 |
nh cl | 4 |
purification kit | 4 |
influenza outbreaks | 4 |
porcine pseudorabies | 4 |
rna sample | 4 |
quantitative lamp | 4 |
equipped labs | 4 |
aluminum foil | 4 |
extension amplification | 4 |
infection control | 4 |
primer bip | 4 |
one nasopharyngeal | 4 |
warmstart rtx | 4 |
lfd assays | 4 |
sequence identity | 4 |
subsequent rt | 4 |
diagnostically useful | 4 |
artery stenosis | 4 |
performed according | 4 |
sequences available | 4 |
ndv qrt | 4 |
extraction protocols | 4 |
positive specimens | 4 |
final products | 4 |
washing buffer | 4 |
naturally infected | 4 |
linear curve | 4 |
different stages | 4 |
higher positive | 4 |
fluorescence monitoring | 4 |
activate autophagy | 4 |
sporadic cases | 4 |
adhesive foil | 4 |
viral copy | 4 |
time fluorometer | 4 |
pathogenic role | 4 |
sputum specimen | 4 |
diseases autophagy | 4 |
pigs infected | 4 |
developed lamp | 4 |
acid releasing | 4 |
several inverted | 4 |
labeled primer | 4 |
culture supernatant | 4 |
human health | 4 |
death mechanisms | 4 |
various clinical | 4 |
preceding stroke | 4 |
prv wild | 4 |
reaction occurs | 4 |
cell entry | 4 |
template controls | 4 |
assay sensitivity | 4 |
bp fragment | 4 |
strand rna | 4 |
many countries | 4 |
barr virus | 4 |
superscript iii | 4 |
two distinct | 4 |
authors acknowledge | 4 |
optical density | 4 |
human transmission | 4 |
throat swab | 4 |
fully scalable | 4 |
corona virus | 4 |
nanopore target | 4 |
mm naoh | 4 |
ncov igm | 4 |
standards ranging | 4 |
aerosol contaminants | 4 |
assay exhibited | 4 |
diagnostic kits | 4 |
samples detection | 4 |
cation assay | 4 |
first step | 4 |
new york | 4 |
every participant | 4 |
within minutes | 4 |
crick institute | 4 |
regression analysis | 4 |
circulating dna | 4 |
like products | 4 |
various pathogens | 4 |
inoculum concentration | 4 |
amplification buffer | 4 |
amplifies dna | 4 |
various rna | 4 |
pbmcs isolated | 4 |
clinically suspected | 4 |
two groups | 4 |
recent studies | 4 |
processing steps | 4 |
also suitable | 4 |
many rt | 4 |
internal primer | 4 |
rtx reverse | 4 |
therapeutic strategies | 4 |
newly synthesized | 4 |
assay established | 4 |
maintaining homeostasis | 4 |
rna polymerases | 4 |
inhibitory effects | 4 |
reported sample | 4 |
biological samples | 4 |
water buffalo | 4 |
virus comparison | 4 |
guangdong provincial | 4 |
amplification curve | 4 |
stroke patients | 4 |
sickle cell | 4 |
therapeutic effects | 4 |
data processing | 4 |
spike gene | 4 |
either dna | 4 |
six independent | 4 |
qpcr positive | 4 |
francis crick | 4 |
using direct | 4 |
synthetic viral | 4 |
autophagy regulators | 4 |
autophagic flux | 4 |
mix consisted | 4 |
fast detection | 4 |
avian respiratory | 4 |
current study | 4 |
hairy nymphae | 4 |
future prospects | 4 |
conventional snp | 4 |
biomedical research | 4 |
encephalitis viral | 4 |
igm antibodies | 4 |
south india | 4 |
lung injury | 4 |
considered positive | 4 |
widely applied | 4 |
test lines | 4 |
rna isolated | 4 |
related coronaviruses | 4 |
effusion samples | 4 |
unless otherwise | 4 |
commercial lamp | 4 |
signal acquisition | 4 |
initial stage | 4 |
green channel | 4 |
validated loop | 4 |
used directly | 4 |
lg ml | 4 |
specimens obtained | 4 |
studies showed | 4 |
ethical committee | 4 |
surgically resected | 4 |
taq dna | 4 |
initiation factor | 4 |
cfu tube | 4 |
fungicide applications | 4 |
virus lysis | 4 |
displaced strand | 4 |
rna tissue | 4 |
blind manner | 4 |
coronavirus outbreak | 4 |
positives due | 4 |
coronavirus development | 4 |
seen whether | 4 |
inducing autophagy | 4 |
assay evaluation | 4 |
per cycle | 4 |
dengue igg | 4 |
positive sense | 4 |
broad antiviral | 4 |
several nucleic | 4 |
acid isolation | 4 |
high sequence | 4 |
glycoprotein gene | 4 |
different sizes | 4 |
pcr plate | 4 |
methods based | 4 |
higher ct | 4 |
tte uvrd | 4 |
practical applications | 4 |
accurately detect | 4 |
lamp uses | 4 |
different samples | 4 |
fluorescent signals | 4 |
treated blood | 4 |
mg ml | 4 |
target sequencing | 4 |
standard strains | 4 |
two regions | 4 |
microfluidic platform | 4 |
experimental procedures | 4 |
necator inoculum | 4 |
transparent adhesive | 4 |
human dna | 4 |
improved sensitivity | 4 |
genetic disorders | 4 |
genetically modified | 4 |
hnb respectively | 4 |
cold chain | 4 |
high cost | 4 |
additional advantage | 4 |
bead stock | 4 |
buffer containing | 4 |
based diagnostic | 4 |
reverse complement | 4 |
short period | 4 |
inflammatory bowel | 4 |
also useful | 4 |
service improvement | 4 |
edwardsiella tarda | 4 |
yielding inconsistent | 4 |
ph change | 4 |
economic losses | 4 |
virus using | 4 |
relatively small | 4 |
respiratory infection | 4 |
restriction enzymes | 4 |
lamp kits | 4 |
fl uorescence | 4 |
emergent carotid | 4 |
digital loop | 4 |
suspected clinically | 4 |
enhance autophagy | 4 |
promotes apoptosis | 4 |
bead capture | 4 |
reference material | 4 |
sophisticated equipment | 4 |
autophagy suppresses | 4 |
apoptosis induced | 4 |
seven clinical | 4 |
two patients | 4 |
autophagic pathway | 4 |
based probe | 4 |
detect pathogens | 4 |
flow control | 4 |
polymorphism genotyping | 4 |
ileumecaecal junction | 4 |
amplifies nucleic | 4 |
low sensitivity | 4 |
rapid tests | 4 |
isolation methods | 4 |
nonstructural protein | 4 |
dna dye | 4 |
autophagy controls | 4 |
zikv infections | 4 |
west africa | 4 |
antiviral drug | 4 |
mass testing | 4 |
handheld lamp | 4 |
important roles | 4 |
ct cutoff | 4 |
threshold value | 4 |
early identification | 4 |
atg complex | 4 |
beads packed | 4 |
first evaluated | 4 |
access holes | 4 |
samples detected | 4 |
strains prv | 4 |
guanidinium thiocyanate | 4 |
four negative | 4 |
gold particles | 4 |
neurological signs | 4 |
suspected cases | 4 |