ライフサイエンスコーパス: copy

1 licated by the fact that males only have one copy.

2 /- 0.44 mm Hg (pcom = 0.01) per risk variant copy.

3 gence and expression difference of duplicate copies.

4 equal expression of the two chromosomal gene copies.

5 units in addition to the native Hordeum rDNA copies.

6 inguish between CAM-related and non-CAM gene copies.

7 ELL gene with different number of functional copies.

8 rkably large and contain multiple chromosome copies.

9 ications, as well as for different number of copies and copy-neutral loss-of-heterozygosity (LOH).

10 ets of epigenetic regulation into (i) single copy and methylated exclusively at CpGs, readily forming

11 mbination differ considerably between single-copy and tandemly-repeated genes.

12 DNA is a remarkably precise medium for copying and storing biological information.

13 template is precisely defined, processively copied, and regenerated by release of single-stranded pr

14 mbination decreased the number of bound L7Ae copies, and either eliminated or changed the L7Ae footpr

15 One of the three SMN2 copies appears to have been converted from SMN1, but exc

16 er genetic variants determining amylase gene copies are associated with 2-year changes in adiposity a

17 These are then copied as RNA and exported to manufacture new proteins.

18 Using a single-copy assay, we measured HIV-1 RNA levels in CSF and plas

19 uL and detectable plasma HIV-1 RNA by single-copy assay.

20 etermined the number of CFHR3 and CFHR1 gene copies by quantitative PCR and collected clinical and bi

21 Tens to thousands of DNA copies can be reliably quantified with excellent single-

22 Instead of copying demonstrators moving balls over long distances,

23 y purification of a sequence-specific single-copy endogenous chromosomal locus containing a DNA doubl

24 a 95% detection probability were 11.5 genome copy equivalents (GCE)/ml (95% fiducial limits, 7.9 to 2

25 n widely observed that sex-related genes are copied from sex chromosomes and inserted into autosomes,

26 during DNA synthesis and exchanges with free copies from solution.

27 t kinetic steps of transcription on a single-copy gene in vivo.

28 ative PCRs and a telomere-sequence to single-copy-gene-sequence ratio method to determine telomere le

29 We propose that co-option of single-copy genes may be a common but relatively understudied m

30 Engineered polymerases that can copy genetic information between DNA and xeno-nucleic ac

31 that production and packaging of the single-copy genome into gametes during the second meiotic divis

32 ces in amylase amount and activity, and AMY1 copies have been associated with adiposity.

33 Among them, five copies have undergone pseudogenization by various mutati

34 h 2 genital specimens each containing >/=105 copies herpes simplex virus DNA/ml collected a median of

35 We generated data for all gene copies (homeologs, paralogs, and segregating alleles) pr

36 he chromosome can be present at thousands of copies in a single cell (in contrast to two copies of nu

37 ates the physical mapping of amplified EPSPS copies in A tuberculatus.

38 ose BCGM by the higher- and lower-expression copies in the mutant.

39 his aim, we coupled mobilization of a single-copy inactivating Sleeping Beauty transposon to Pten dis

40 the growing duplex as the template strand is copied into XNA.

41 pic changes in metabolism following a single copy knock-in of mutant PIK3CA (H1047R) in the MCF10A ce

42 of detection of 3.40 +/- 0.20 log10 genomic copies (LGC), which is comparable to most other reported

43 iated gene dependencies and identify partial copy-loss of wild-type SF3B1 as a novel, non-driver canc

44 mptomatic cases were approximately 1-2 log10 copies lower than in symptomatic cases.

45 ic coastal upwelling for OI (36 713 +/- 1485 copies ml(-1) ) and the Kuroshio Front for OII (50 189 +

46 d the Kuroshio Front for OII (50 189 +/- 561 copies ml(-1) ) and the two overlapped only in frontal r

47 -1 RNA increased from <20 copies/mL to >1500 copies/mL (range, 21-1571 copies/mL) during treatment.

48 HIV RNA of 36 copies/mL that rose to 59,805 copies/mL 6 days later.

49 apped substantially (range, 0.16-989.9 x 103 copies/mL and 0.01-551.9 x 103 copies/mL, respectively).

50 The probability of confirmed HIV RNA >1000 copies/mL by 48 months was 0.07 and 0.12 in the EFV and

51 re 19.3 copies/ml for the 1-ml assay and 126 copies/ml for the 0.175-ml assay.

52 ties determined by probit analysis were 19.3 copies/ml for the 1-ml assay and 126 copies/ml for the 0

53 detection of 1000 copies/mL in semen and 275 copies/mL in blood.

54 e assay produced limits of detection of 1000 copies/mL in semen and 275 copies/mL in blood.

55 T at the WHO-recommended threshold of >1,000 copies/ml on the Roche CAP/CTM system.

56 oportion who died or had a viral load of 400 copies/mL or higher at 12 months post-ART initiation was

57 d subjects with plasma viremia of <3,000 RNA copies/ml over 17 to 179 weeks.

58 or 7.4 months, rebounding with HIV RNA of 36 copies/mL that rose to 59,805 copies/mL 6 days later.

59 cipants, plasma HIV-1 RNA increased from <20 copies/mL to >1500 copies/mL (range, 21-1571 copies/mL)

60 ing retained at 12 months with HIV-1 RNA <50 copies/ml was 1.21 (95% CI: 1.04, 1.38; p = 0.015) for t

61 Pneumococcal colonization density >6.9 log10 copies/mL was strongly associated with MCPP and could be

62 yses described the incidence of major (>1000 copies/mL) and minor (50-1000 copies/mL) viremic episode

63 lers (ie, persons with a viral load of </=40 copies/mL) and noncontrollers, antibody parameters were

64 copies/mL to >1500 copies/mL (range, 21-1571 copies/mL) during treatment.

65 56 cases with MCPP (MCPP cases; 17.28 x 106 copies/mL) exceeded that of cases without MCPP (non-MCPP

66 f major (>1000 copies/mL) and minor (50-1000 copies/mL) viremic episodes (VEs) and factors associated

67 n with VEs, peak viremia (median, 3.79 log10 copies/mL) was linearly related to pre-ART VL.

68 (adjPRR) of detectable HIV shedding (VL > 40 copies/mL) were estimated by Poisson regression models w

69 an controls (median, 4.0 x 103 vs 0.19 x 103 copies/mL), but overlapped substantially (range, 0.16-98

70 he height of the neurological symptoms (1.5E copies/mL).

71 th undetectable plasma viral load (pVL) (<20 copies/ml).

72 tage 3 who became virally suppressed (</=200 copies/mL).

73 At <1000 copies/ml, agreement between DBS and plasma was 96.7% (k

74 6-989.9 x 103 copies/mL and 0.01-551.9 x 103 copies/mL, respectively).

75 nt samples was shown from 1.54 to 6.93 log10 copies/ml.

76 sure of VL and ARV status (VL <400 or >/=400 copies/mL; ARV therapy or no ARV therapy).

77 s well as for different number of copies and copy-neutral loss-of-heterozygosity (LOH).

78 first assessed the association between AMY1 copy number (genotyped by digital droplet polymerase cha

79 d volume were positively associated with CR1 copy number (mean number of CR1 molecules per erythrocyt

80 ich can lead to changes in mitochondrial DNA copy number (mtDNAcn).

81 Then we inferred the changes in gene copy number (N), syntenies, and tuning sites along each

82 ed bees (7.45*10(12) +/- 1.62*10(12) average copy number +/- standard error) compared to other tested

83 igned to detect driver mutations, chromosome copy number aberrations, and mutation signatures.

84 Copy number alteration (CNA) is a major contributor to g

85 tween immune metagene expression and somatic copy number alteration levels (rho = -0.484, P = 2 x 10-

86 ncordance of clonal somatic mutations (88%), copy number alterations (80%), mutational signatures, an

87 We stratify mutations and copy number alterations for important kidney cancer gene

88 netic basis for immune evasion: near-uniform copy number alterations of chromosome 9p24.1 and the ass

89 ct primary tumors and did not harbor similar copy number alterations or demonstrate significant mutat

90 re frequently targeted by somatic mutations, copy number alterations, DE and AS, indicating their pro

91 aracterized by increased accumulation of DNA copy number alterations, greater genetic diversity and i

92 d did not show a bias to regions involved in copy number alterations.

93 ration sequencing studies for mutational and copy number analysis.

94 in the group of participants with a low AMY1 copy number and a high dietary intake of starch.Our find

95 and its target genes (IL8, CSF2), and TRIB1 copy number and expression were predictive of clinical o

96 d with 528 genes having correlations between copy number and gene expression.

97 ecDNA amplification would increase oncogene copy number and intratumoural heterogeneity more effecti

98 We investigated the association between AMY1 copy number and obesity traits, and the effect of the in

99 phenome-wide association studies, as well as copy number and rare variant analyses.

100 icant effect of the interaction between AMY1 copy number and starch intake on BMI (P-interaction = 0.

101 d the effect of the interaction between AMY1 copy number and starch intake on these obesity traits.We

102 nslated region (UTR), which affect both mRNA copy number and translation.

103 d by targeted next-generation sequencing and copy number array.

104 pan of Tk2-deficient mice and restored mtDNA copy number as well as respiratory chain enzyme activiti

105 We hypothesised that EGFR copy number by fluorescence in-situ hybridisation (FISH)

106 eneration sequencing analysis of chromosomal copy number changes and mutations is useful in distingui

107 We used gene expression and copy number data to infer pathway activities for cell li

108 Neither the copy number differences nor the rearrangements were obse

109 trotransposons (RTs) can rapidly increase in copy number due to periodic bursts of transposition.

110 Moreover, copy number elevations of COMT or Tbx1 reduced the proli

111 ovide evidence for the novel hypothesis that copy number elevations of these 22q11.2 genes alter the

112 Interestingly, we do not observe the extreme copy number expansion of the AMY2B gene characteristic o

113 tinib with that of placebo according to EGFR copy number gain (CNG) and EGFR, KRAS, BRAF, and PIK3CA

114 NVs were found in <1.5% of brains, including copy number gains of PRPH that were overrepresented in A

115 gree of aneuploidy and is partly due to gene copy number imbalances, suggesting that subtle changes i

116 Gene copy number impacts on gene expression were detected wit

117 rial fragmentation and reduced ATP and mtDNA copy number in FECD.

118 expression correlated with increased genomic copy number in SCLC lines.

119 Sal-1, one such fragment with the highest copy number in the infected cells, is derived from Salmo

120 (Rho = 0.3531; P = 0.0218) and the proviral copy number in the peripheral blood as an indirect measu

121 mple and accurate determination of transgene copy number in these six important crop species.

122 DNA methylation and copy number integration with transcript levels yielded a

123 First, the copy number is estimated by maximum likelihood and assoc

124 ity of NLRC5 caused by promoter methylation, copy number loss, or somatic mutations is associated wit

125 te that this approach can generate confident copy number measurements in independent transgenic lines

126 The results indicate a copy number of 25 for FliG.

127 Somatic copy number of 8 genes frequently deleted in ALL (CDKN2A

128 We therefore suggest that the copy number of HIV in 8E5 extracts be established by dPC

129 ar to affect gene expression by altering the copy number of intergenic regulatory regions.

130 re observed in a clinical sample with a high copy number of JCV or a plasmid control.

131 e interaction between starch intake and AMY1 copy number on obesity.

132 In addition, we show copy number profiles can also be obtained from the same

133 onal changes are supported by mutational and copy number profiles in breast cancers.

134 STmiR sensors were also used to estimate the copy number range of miRNAs in total RNA extracts.

135 ailure and heart failure, we estimated GSTM1 copy number using exome sequencing reads in the Atherosc

136 Copy number variable genes tended to be evolutionarily r

137 on of novel variants among smaller and rarer copy number variable segments.

138 The effect of Copy Number Variants (CNVs) on Type 2 Diabetes (T2D) rem

139 We show that copy number variants (CNVs) show a variety of genetic si

140 microscopic genomic rearrangements including copy number variants (CNVs).

141 Rare copy number variants contribute significantly to the ris

142 Analysis of copy number variants detected 5.2 deletions and 10.3 amp

143 Duplication and triplication of copy number variants of 22q11.2 are consistently and rob

144 rences in single-nucleotide polymorphisms or copy number variants, respectively, for differential dis

145 iant could be accelerated by the presence of copy number variation (CNV) at the K3L locus, which in m

146 Gene copy number variation (CNV) has been shown to be associa

147 Recently copy number variation (CNV) has gained considerable inte

148 Copy number variation (CNV) is an important cause of neu

149 sponding region in horse shows extraordinary copy number variation and different relative location an

150 The resulting DNA copy number variation and patterns of chromosome loss an

151 on, DNA methylation, noncoding microRNA, and copy number variation data available from the Gene Expre

152 ceptibility to IAV segregates independent of copy number variation in multicopy ChrY gene families th

153 ic loci with extensive nucleotide diversity, copy number variation of paralogous genes, and long repe

154 Copy number variation of the target loci may be another

155 3A/E6AP-dependent ASD.SIGNIFICANCE STATEMENT Copy number variation of the UBE3A gene and aberrant ove

156 orroborative pattern between the chromosomal copy number variation profiles of the AH cfDNA and tumor

157 latform, followed by genome-wide chromosomal copy number variation profiling to assess the presence o

158 Copy number variation was rampant with between 16 098 an

159 athways, compounds, quantitative proteomics, copy number variation, and polysomal transcriptomics.

160 rovides an evolutionary alternative for gene copy number variation.Eukaryotic cells rely on the ubiqu

161 neity, total mutation load, neoantigen load, copy number variations (CNV), gene- or pathway-level som

162 hed array data from the 60 samples show that copy number variations (CNVs) and alterations in DNA met

163 Copy number variations (CNVs) have recently been linked

164 microdeletion is among the most common gene copy number variations (CNVs) known to confer risk for i

165 ingle-nucleotide polymorphisms (SNPs) and 43 copy number variations (CNVs) with in-vitro piperaquine

166 ould be determined and 7.2% of these carried copy number variations and/or chromosomal abnormalities,

167 quences by Illumina paired-reads sequencing, copy number variations by qPCR, RNA concentrations by qR

168 K2 is one of the genes in the 16p11.2 locus, copy number variations of which are associated with auti

169 we report the first observation of abundant copy number variations on neuropeptides and receptors, w

170 and 12.6 de novo insertions and deletions or copy number variations per ASD subject.

171 AMY1 and AMY2 show copy number variations that affect differences in amylas

172 les, 215 genes spanning rare and replication copy number variations, 99 genes overlapping with linkag

173 are significantly correlated with their gene copy number variations.

174 ers a unique opportunity to quantify protein copy number with nanoscale resolution.

175 m likelihood and association of the expected copy number with the phenotype is tested.

176 stimated that decreases in mitochondrial DNA copy number, a measure of mitochondrial genome abundance

177 and adenovirus receptor) expression and CVB3 copy number, and an improved left ventricular function i

178 the CVB3-induced inflammatory response, CVB3 copy number, and apoptosis in vitro.

179 and analyzed mRNA and miRNA expression, DNA copy number, and DNA methylation in 117 Wilms tumors, fo

180 es from 10 cases, the mutational signatures, copy number, and SNV mutational profiles reflect the exp

181 in respiratory activity: depletion of mtDNA copy number, decreases in mtRNA levels, and decreases in

182 ctivity or, through incrementally increasing copy number, may be sites of secondary selective pressur

183 biological samples, such as gene expression, copy number, methylation etc.

184 thereby leading to false-positive results in copy number-amplified regions.

185 criptome impacted by allele preferential and copy number-dependent expression effects.

186 nd loci, CD274/PD-L1 and PDCD1LG2/PD-L2, and copy number-dependent increased expression of these liga

187 ssentiality screens while accounting for the copy number-specific effect.

188 sted for the covariates of age and MYCN gene copy number.

189 and selects for a progressively higher BRAF copy number.

190 rdings are not sensitive to decreased Chrna7 copy number.

191 amatically improved in GT mice with a vector copy number/genome higher than 1 in the BM and 2 in the

192 ve from chemorefractory disease, we examined copy-number aberrations (CNAs) in circulating tumor cell

193 Extensive prior research focused on somatic copy-number alterations (SCNAs) affecting cancer genes,

194 somatic point mutations, but rather somatic copy-number alterations (SCNAs).

195 Cohort samples had extensive copy-number alterations and highly recurrent somatic mut

196 ad intratumor heterogeneity for both somatic copy-number alterations and mutations.

197 Multiple somatic mutations and copy-number alterations in genes that are therapeutic ta

198 ssess the phenotypic consequences of genomic copy-number alterations that are repeatedly observed in

199 After integration of somatic copy-number alterations, and clinical features specific

200 lted in parallel evolution of driver somatic copy-number alterations, including amplifications in CDK

201 These data provide a catalog of copy-number associated gene dependencies and identify pa

202 sarcoma) are characterized predominantly by copy-number changes, with low mutational loads and only

203 cability to cancer samples with frequent DNA copy-number changes.

204 Copy-number gain at 3q resulted in increased MAP3K13 mRN

205 Elevated copy-number heterogeneity was associated with an increas

206 limited application in the detection of low-copy-number pathogens in complex samples.

207 ed localization microscopy to studies of low-copy-number proteins in living bacteria.

208 We also identified copy-number variant (CNV) eQTLs, including some that app

209 Coldspots are strongly associated with copy-number variant (CNV) regions, especially multi-alle

210 y-matched controls for rare (< 1% frequency) copy-number variants (CNVs) using SNP microarray data.

211 Africa, we identify a diverse array of large copy-number variants affecting the host invasion recepto

212 analyses show six genes that have recurrent copy-number variants in three squamous-cell carcinomas (

213 Causal copy-number variants were found in 12 patients (11.9%) w

214 (WGA) methods are limited by low accuracy of copy-number variation (CNV) detection and low amplificat

215 parasites, in addition to variations in DNA copy-number.

216 positively correlated with proviral HIV-DNA copy numbers in peripheral blood mononuclear cells (PBMC

217 ve evolutionary strategy to rapidly increase copy numbers of genomes per cell at the expense of the t

218 rison of genes and repeats unveiled that the copy numbers of NLRs were greatly increased by LTR-retro

219 Copy numbers of the FCGR2A and FCGR2C genes were signifi

220 te polymerase production will produce higher copy numbers of the improved partner gene.

221 The distribution and copy numbers of the virus appear to correlate with urina

222 e integrated mutations, gene expression, DNA copy numbers, DNA methylation and protein abundance, all

223 Plasmids containing multiple copies of (G3T)n and (G3T4)n repeats, were probed with d

224 olyploid species to combine mutations in all copies of a gene (homoeologs), and to expose phenotypic

225 erance of the loss of one or both functional copies of a gene is related to the gene's causal role in

226 erated mice overexpressing either one or two copies of a kinase-dead mTOR mutant (KD-mTOR) transgene

227 The heralded generation of two copies of a remote entangled state is demonstrated throu

228 It contains two homologous copies of a six-transmembrane-helix (6-TM) domain, which

229 s, the latter of which have given rise to 12 copies of alpha-gliadin genes clustered within a 550-kb

230 ngle dose of 5 x 10(12) or 2 x 10(13) genome copies of AMT-060/kilogram was administered to 5 partici

231 eptide epitopes (SunTag) recruiting multiple copies of antibody-fused de novo DNA methyltransferase 3

232 Loss of both copies of B2M is found only in non-responders.

233 mpared with those whose tumors had wild-type copies of both genes, although only results for BRAFV600

234 n conditioning expression divergence between copies of duplicates generally holds for duplicates gene

235 3F appear to be copies of each other as they share the identical arrange

236 TR lncRNAs transcribed from many of the 4000 copies of ERV-9 LTR retrotransposons acted by a similar

237 of small RNAs in live, single cells, tandem copies of FASTmiR122 were expressed in different cell li

238 ner, we used groES (7), a gene linking seven copies of groES, to incorporate I25 mutations in selecte

239 The loss of one or both copies of GSTM1 is common in many populations and has be

240 we show that hGW182 can recruit up to three copies of hAgo via its three GW motifs.

241 rences per 10,000 base pairs between the two copies of her genome, fewer than present-day humans, sug

242 kg or more, had virological suppression (<50 copies of HIV-1 RNA per mL) on a stable regimen for at l

243 copies in a single cell (in contrast to two copies of nuclear chromosomes), and mtDNA deletions may

244 , evidencing that as little as a few tens of copies of redox-labeled macromolecules immobilized on in

245 l to combined endpoint in SMA infants with 2 copies of SMN2 indicated a median age of 8 months at dea

246 this example is an inductive limit of unital copies of the Cuntz algebra [Formula: see text] or of th

247 During varphiX174 morphogenesis, 240 copies of the external scaffolding protein D organize 12

248 L evolution, both models acquired additional copies of the mutant Flt3 or Nras alleles, but only Npm1

249 back process, methods to efficiently add new copies of the relevant gene to hematopoietic stem cells

250 rue when the competition stems from multiple copies of the same gene.

251 these multi-particle images are comprised of copies of the same particles.

252 tronic states emerge as a result of multiple copies of the TOTA(+) making pi-contact with cyanostar-a

253 mitosis, cells must segregate the replicated copies of their genome to their daughter cells with extr

254 etermined structures can interact with other copies of themselves and assemble into homomeric complex

255 electron microscopy, demonstrating that two copies of VirD4 dimers locate on both sides of the appar

256 This indicated that 2 copies of Zeb2 are required for EDN3 to prevent neuronal

257 One functional copy of GATA6 is sufficient for definitive endoderm deve

258 also analyzed from mice that express only 1 copy of human REG3A transgene but were fed feces from co

259 nd used recombineering to reintegrate a full copy of the gene, generating the {for(BAC)} rescue allel

260 of ataxin 7 and replace it with an exogenous copy of the gene, highlighting the efficacy and transfer

261 th rs147210663 was particularly strong; each copy of the Thr allele conferred 42% lower triglycerides

262 Mutations truncating a single copy of the tumor suppressor, BRCA2, cause cancer suscep

263 Gene conversion is the copying of a genetic sequence from a "donor" region to a

264 ted RNA primer extension, allowing efficient copying of a variety of short RNA templates with mixed s

265 Despite recent progress, the nonenzymatic copying of templates containing mixed sequences remains

266 sma HIV-1 RNA concentrations of less than 50 copies per mL at week 24 according to the US Food and Dr

267 ipants with plasma HIV-1 RNA of less than 50 copies per mL at week 48 (assessed by the US Food and Dr

268 ipants with plasma HIV-1 RNA of less than 50 copies per mL at week 48 (US Food and Drug Administratio

269 ir group had HIV-1 RNA loads of less than 50 copies per mL compared with 31 (93.9%) of 33 in the dolu

270 NRTI group had viral loads of less than 400 copies per mL compared with 312 (81%) of 383 in the prot

271 proportion of participants with less than 50 copies per mL of plasma HIV-1 RNA at week 48 (by the US

272 ological rebound (confirmed viral load >/=50 copies per mL or premature discontinuations, with last v

273 ained virological suppression (HIV-1 RNA <50 copies per mL) at week 24.

274 discontinuations, with last viral load >/=50 copies per mL) cumulative through week 48; we tested non

275 ment of a single viral load of more than 200 copies per mL, and 1414 (31%) by a documented treatment

276 ntiretrovirals and had HIV RNA less than 200 copies per mL, or not receiving antiretrovirals and had

277 with virological suppression of less than 50 copies per mL.

278 (36.7%) had viral loads of more than 50 000 copies per mL.

279 78%) of 375 had viral loads of less than 400 copies per mL; p=0.003 versus the protease inhibitor plu

280 s directly estimate the number of DNA target copies per reaction partition, lambda, where the partiti

281 from samples containing as few as 50 genome copies per reaction.

282 CAPZB, present at approximately 100 copies per stereocilium, concentrated at stereocilia tip

283 cifically, the sheer abundance of genomic L1 copies prevents reliable quantification of new insertion

284 nerating site-specifically integrated single-copy promoter transgenes and measuring their expression

285 shown to be lower in the IR than the single copy regions (SC).

286 Inversion polymorphisms between low-copy repeats (LCRs) might predispose chromosomes to meio

287 neous distribution of these new retroelement copies result from a combination of two mechanisms, of w

288 , such as proprioceptive and motor efference copy signals, including gaze-related information.

289 on (CNV) at the K3L locus, which in multiple copies strongly reduced PKR activation.

290 demonstration conditions some children also copied the demonstrated tower.

291 in VP1, which is the enzyme responsible for copying the viral RNA genome.

292 the nucleus are locations where viral DNA is copied to support virus persistence and amplification of

293 phase, whereas MIND and Ndc80 submodules add copies to form an "anaphase configuration" kinetochore.

294 Single-copy transgenes that express rde-4(+) in body-wall muscl

295 correlate with learning ability - males that copied tutor songs more accurately had more bridge neuro

296 RR for being retained with HIV-1 RNA <1,000 copies was 1.18 (95% CI: 1.04, 1.31; p = 0.012).

297 0min, and the limit of detection was only 11 copies with a volume of 30muL.

298 tal action - is associated with an efference copy with detailed auditory properties.

299 it of detection of 9.8pg of soybean DNA (8.6 copies), with adequate real-time PCR performance paramet

300 e relatively small-scale polymorphism of ITS copies within individuals has often been reported in lit