1 and greater genetic diversity as assessed by
DNA sequence analysis.
2 Bw4 expression was confirmed by
DNA sequence analysis.
3 potential to replace gel electrophoresis for
DNA sequence analysis.
4 road range of vertebrate poikilotherms using
DNA sequence analysis.
5 etry, accurate mass measurements, and direct
DNA sequence analysis.
6 eteroduplex mobility and tracking assays and
DNA sequence analysis.
7 , and characterization of point mutations by
DNA sequence analysis.
8 the heteroduplex mobility assay (HMA) and by
DNA sequence analysis.
9 are not sufficiently similar to identify by
DNA sequence analysis.
10 DNAs, and locating primer binding sites for
DNA sequence analysis.
11 oaches, 71 by microarray and 63 by gel-based
DNA sequence analysis.
12 olated the tumor cells and subjected them to
DNA sequence analysis.
13 12 genes in four operons were identified by
DNA sequence analysis.
14 hin slab gel electrophoresis-based automated
DNA sequence analysis.
15 K-ras mutations were determined by
DNA sequence analysis.
16 other nanopore devices for implementation of
DNA sequence analysis.
17 omes and is an economic tool for comparative
DNA sequence analysis.
18 Discrepant results were resolved by
DNA sequence analysis.
19 Identification was based on morphology and
DNA sequence analysis.
20 finally to mutant allele characterization by
DNA sequence analysis.
21 qacA or qacB gene was determined by PCR and
DNA sequence analysis.
22 F MS for automated high-throughput microbial
DNA sequence analysis.
23 Length of the products was confirmed by
DNA sequence analysis.
24 es with positive H. pylori were subjected to
DNA sequencing analysis.
25 solutions were used as sieving matrixes for
DNA sequencing analysis.
26 arget site was estimated to be 20% by direct
DNA sequencing analysis.
27 sults were consistent with those obtained by
DNA sequencing analysis.
28 ytes and macrophages, which was confirmed by
DNA sequencing analysis.
29 olled to achieve high performance and rugged
DNA sequencing analysis.
30 d MLL-AF4-encoded proteins based on previous
DNA sequencing analysis.
31 anis using PCR, multiplex real-time PCR, and
DNA sequencing analysis.
32 Based upon
DNA sequence analysis,
a Mycoplasma ovis-like species wa
33 ations of these mutations were determined by
DNA sequence analysis after PCR amplification of the pho
34 Furthermore,
DNA sequence analysis allowed the determination of the p
35 l language processing (NLP), (ii) predictive
DNA sequence analysis and (iii) Human activity recogniti
36 utated by microarray but not by conventional
DNA sequence analysis and 6 cases identified as mutated
37 roteins and synthetic peptides based on this
DNA sequence analysis and examined their reactivity with
38 luated in 108 ovarian tumors by conventional
DNA sequence analysis and oligonucleotide microarray (p5
39 DNA sequence analysis and restriction mapping of one par
40 DNA sequence analysis and site-directed mutagenesis stud
41 have been validated by gel electrophoresis,
DNA sequence analysis and thermal denaturation profile.
42 al samples is a bottleneck in genotyping and
DNA sequencing analysis and is frequently limited by the
43 ing STS-content mapping, comparative genomic
DNA sequence analysis,
and cDNA cloning, we found that t
44 upted genes in 51 mutants were identified by
DNA sequence analysis,
and the mutations included interr
45 sed unambiguously, comparative mitochondrial-
DNA-sequence analysis appears to be a reliable and power
46 AMOS project has released several innovative
DNA sequence analysis applications including: Hawkeye, a
47 ng compared with methods that do not require
DNA sequencing analysis as an additional step and that h
48 Cosmids are annotated by
DNA sequence analysis at the transposon insertion sites,
49 odology of earlier studies relied largely on
DNA sequence analysis but lacked functional assays of du
50 cases identified as mutated by conventional
DNA sequence analysis but not by microarray.
51 DNA sequence analysis by oligonucleotide binding is ofte
52 High-throughput
DNA sequence analysis can potentially identify all sourc
53 DNA sequence analysis confirmed TCC-specific mutations i
54 The
DNA sequence analysis confirmed that the polymerase chai
55 DNA sequence analysis confirmed the integration of ACME
56 Conventional
DNA sequence analysis demonstrated an 87% accuracy rate,
57 DNA sequence analysis demonstrated that the RTX locus is
58 DNA sequence analysis demonstrated that this region cont
59 We performed
DNA sequence analysis,
differential polymerase chain rea
60 DNA sequence analysis established that all three 60A all
61 rologous expression in Escherichia coli, and
DNA sequence analysis excluded cis-acting mutations as t
62 DNA sequence analysis failed, however, to identify the R
63 Based on
DNA sequence analysis,
fit encodes an outer membrane pro
64 In addition,
DNA sequence analysis formally demonstrated a loss of di
65 PCR and
DNA sequence analysis found that Spy1325 is very well co
66 DNA sequence analysis from -3.8 to -7.2 kb identified fi
67 Here we have used PCR
DNA sequence analysis from multiple segments of DNA ampl
68 be grown in cell culture, but by direct PCR
DNA sequence analysis from segments totaling 15 to 30% o
69 DNA sequence analysis,
gel mobility shifting, chromatin
70 DNA sequence analysis grouped this orf virus isolate amo
71 The deduced proteins, based on
DNA sequence analysis,
have molecular masses of 13 and 2
72 DNA sequence analysis identified 38 laf genes in two loc
73 Genomic
DNA sequence analysis identified conserved E2F consensus
74 DNA sequence analysis identified two different mutations
75 ola virus orthopoxviruses were positive, and
DNA sequence analysis implicated a novel orthopoxvirus s
76 DNA sequence analysis,
in combination with genetic compl
77 ranscriptase-dependent nested PCR, including
DNA sequence analysis,
in situ hybridization, and immuno
78 DNA sequence analysis indicated that most of the mutatio
79 Characterization of the sde locus by
DNA sequence analysis indicated that the Omega4408 inser
80 norubicin-producer Streptomyces peucetius by
DNA sequence analysis indicated that these genes encode
81 DNA sequencing analysis indicated that this was a fusion
82 Deoxyribonucleic acid (
DNA) sequencing analysis indicated that this gene contai
83 DNA-sequencing analysis indicated that the Y586F mutatio
84 DNA sequence analysis indicates that both proteins are l
85 Recent
DNA sequence analysis indicates that rhesus rhadinovirus
86 DNA sequence analysis indicates that this region contain
87 One of the main tasks of
DNA sequence analysis is identification of repetitive pa
88 From
DNA sequence analysis,
it was predicted that the transla
89 HTA findings were used to select for
DNA sequence analysis maternal virus populations that we
90 e BACTEC 460TB system combined with standard
DNA sequencing analysis methods for katG, inhA, and rpoB
91 ion, p16 gene inactivation was determined by
DNA sequence analysis,
methylation-specific PCR, and imm
92 clinical sources were evaluated by ribosomal
DNA sequence analysis,
multilocus sequence analysis, DNA
93 DNA sequence analysis of 130 alleles of the HRAS1 minisa
94 DNA sequence analysis of 18 GRD copies reveal 4 distinct
95 length polymorphism (RFLP) analysis of flaA,
DNA sequence analysis of 582 bp of flaA that included th
96 DNA sequence analysis of 66 low-risk a1 alleles revealed
97 DNA sequence analysis of a 2.6-kb portion of the promote
98 used to design a strategy for isolation and
DNA sequence analysis of a 7,886-base pair A. vinelandii
99 ogy has offered the potential for the direct
DNA sequence analysis of a broad spectrum of pathogens o
100 Our
DNA sequence analysis of a major fraction of eleutheroda
101 DNA sequence analysis of a region downstream of exoU ide
102 DNA sequence analysis of amplified ITS1 region DNA from
103 Ancient
DNA sequence analysis of archaeological bottle gourd spe
104 DNA sequence analysis of autism subjects and controls re
105 tyrosine kinase inhibitors that would inform
DNA sequence analysis of candidate tyrosine kinases.
106 DNA sequence analysis of cDNA clones for tRNA(Ser) and 1
107 DNA sequence analysis of cDNA generated by 5'RACE from C
108 DNA sequence analysis of cloned regions of classI mutant
109 During
DNA sequence analysis of cosmid L373 from the Mycobacter
110 DNA sequence analysis of cosmid pLM49 revealed a cluster
111 However,
DNA sequence analysis of crossover junctions indicated t
112 DNA sequence analysis of different clones identified 19
113 DNA sequence analysis of each of the Alu Yd subfamilies
114 t (Mutector; TrimGen, Sparks, MD) and direct
DNA sequence analysis of exon 15 after PCR amplification
115 DNA sequence analysis of exons 2 to 9 of the neuroserpin
116 DNA sequence analysis of four independent isolates revea
117 DNA sequence analysis of fragments obtained by PCR ampli
118 o sort the libraries for active mutants, and
DNA sequence analysis of functional BLIP mutants identif
119 Genomic
DNA sequence analysis of human COX-2 revealed a silent m
120 DNA sequence analysis of intellectual disability patient
121 DNA sequence analysis of its 330, 742-bp genome leads to
122 We hypothesized that
DNA sequence analysis of multiple loci is useful for rap
123 DNA sequence analysis of murA from C. trachomatis predic
124 This method relies on
DNA sequence analysis of nucleotide polymorphisms in hou
125 DNA sequence analysis of one full-length 1.3-kb clone (p
126 rium nucleatum were characterized, including
DNA sequence analysis of one plasmid, pFN1.
127 DNA sequence analysis of ORF99 from each of the existing
128 ecting the 3 family members was confirmed by
DNA sequence analysis of pol, gag, and env genes.
129 DNA sequence analysis of pph1 indicates that it encodes
130 DNA sequence analysis of R. typhi tlyC revealed an open
131 DNA sequence analysis of regions flanking their transpos
132 DNA sequence analysis of representative polyphyletic mar
133 DNA sequence analysis of RRV indicates that it shares nu
134 DNA sequence analysis of spliced LRT cDNAs, poly(A)+ or
135 PCR amplification and
DNA sequence analysis of SRY revealed no mutations in th
136 DNA sequence analysis of tau coding regions in affected
137 DNA sequence analysis of the 1.3-kb region predicted an
138 DNA sequence analysis of the 5.0 kb fragment revealed th
139 DNA sequence analysis of the 5.8 Mb S. arenicola circula
140 DNA sequence analysis of the 51 patients with defective
141 DNA sequence analysis of the bt2-7503 mutant allele of t
142 DNA sequence analysis of the cloned insert revealed a 30
143 This study presents
DNA sequence analysis of the core promoter region for CH
144 DNA sequence analysis of the direct repeat units within
145 DNA sequence analysis of the E. coli flo gene demonstrat
146 DNA sequence analysis of the fibrinogen genes A, B, and
147 DNA sequence analysis of the flk gene has revealed it to
148 e clinical diagnosis of AROA were studied by
DNA sequence analysis of the four classic OCA genes: TYR
149 on-Hispanic Caucasian patients, we performed
DNA sequence analysis of the four genes associated with
150 DNA sequence analysis of the gene for IFNgammaR2 showed
151 DNA sequence analysis of the gene in these 50 isolates f
152 DNA sequence analysis of the genes encoding the MAb reve
153 DNA sequence analysis of the hrp/hrc regions in Psy 61,
154 DNA sequence analysis of the individual Alu elements rev
155 Here we provide a
DNA sequence analysis of the innate immune gene STAT2 an
156 DNA sequence analysis of the internal transcribed spacer
157 DNA sequence analysis of the isolate indicated that it w
158 ms for identifying yeasts, were confirmed by
DNA sequence analysis of the ITS2 region from 93 isolate
159 DNA sequence analysis of the known CCM genes in a cohort
160 Further
DNA sequence analysis of the lpfA1 and lpfA2 genes from
161 DNA sequence analysis of the molecular clones revealed t
162 DNA sequence analysis of the O37 wb* region revealed tha
163 groups has been confirmed and refined by PCR
DNA sequence analysis of the ORF-K1 gene encoding a high
164 Here we report the results of a comparative
DNA sequence analysis of the orthologous human (750 kb)
165 DNA sequence analysis of the orthologous inserts showed
166 DNA sequence analysis of the P. syringae ES4326 rpoN gen
167 DNA sequence analysis of the pbs1-2 allele showed it to
168 Extensive
DNA sequence analysis of the PCGEM1 cDNA and genomic DNA
169 of a genetic alteration, as demonstrated by
DNA sequence analysis of the PCNA gene from malignant an
170 ses detected by this assay were confirmed by
DNA sequence analysis of the PCR amplicons.Results.
171 Previously, we had shown that
DNA sequence analysis of the protein A gene variable rep
172 the puc mRNA transcriptional start site and
DNA sequence analysis of the puc upstream regulatory seq
173 rrelia species as assessed by microscopy and
DNA sequence analysis of the pyrG gene.
174 DNA sequence analysis of the region encoding the tail fi
175 DNA sequence analysis of the region flanking cobB locate
176 DNA sequence analysis of the region immediately upstream
177 Using
DNA sequence analysis of the ribosomal DNA intergenic tr
178 DNA sequence analysis of the RT-encoding region of the p
179 DNA sequence analysis of the S. boydii 0-1392 island, de
180 nstraint, we developed a typing system using
DNA sequence analysis of the serine-aspartate (SD) repea
181 DNA sequence analysis of the Sry ORF and a 5' 800-bp seg
182 DNA sequence analysis of the structural subunit gene afr
183 Genomic
DNA sequence analysis of the uropathogenic Escherichia c
184 DNA sequence analysis of the viral DNA-target junctions
185 DNA sequence analysis of the viral genomes cloned from d
186 lates of Staphylococcus aureus were typed by
DNA sequence analysis of the X region of the protein A g
187 DNA sequence analysis of the zwi-3 mutation indicated th
188 DNA sequence analysis of this Alu fragment revealed that
189 DNA sequence analysis of this clone revealed the identit
190 DNA sequence analysis of this clone, containing a 2.7-kb
191 DNA sequence analysis of this enhancer element revealed
192 DNA sequence analysis of this mutant revealed a transpos
193 DNA sequence analysis of this region identified 13 signi
194 DNA sequence analysis of this region revealed the presen
195 DNA sequence analysis of two SIRE-1 subclones revealed t
196 processed viral DNAs, we performed extensive
DNA sequencing analysis of 2-LTR-circle junctions.
197 By nested methylation-specific
DNA sequencing analysis of lung and breast cancer cell l
198 DNA sequencing analysis of nonfluorescent GFP clones ind
199 entiate C. hominis and C. parvum is based on
DNA sequencing analysis of PCR amplicons.
200 Restriction enzyme mapping, subcloning, and
DNA sequencing analysis of recombinant phage lambda and
201 DNA sequencing analysis of unselected library members re
202 Importantly, high-throughput
DNA sequencing analysis on the transcriptome of ES cells
203 e rapid bacterial identification by targeted
DNA sequence analysis or by whole-genome sequencing perf
204 With near full-length 16S ribosomal
DNA sequence analysis,
organisms cultured from the blood
205 induced mutation spectrum as established by
DNA sequence analysis (
p < 0.005; 95% CI, 0.002-0.009).
206 te 20 of 33 species of molds tested, and ITS
DNA sequence analysis permits identification of all spec
207 on was formed by a simple terminal deletion,
DNA sequence analysis,
pulsed-field gel electrophoresis
208 Most existing methods for
DNA sequence analysis rely on accurate sequences or geno
209 DNA sequence analysis revealed a binding motif for octam
210 ription start site for SR-BI was mapped, and
DNA sequence analysis revealed a binding site for SF-1 i
211 DNA sequence analysis revealed a C to A transversion in
212 DNA sequence analysis revealed a high degree of genetic
213 DNA sequence analysis revealed a missense mutation in th
214 DNA sequence analysis revealed a mosaic nature of the ca
215 DNA sequence analysis revealed a mutation resulting in a
216 DNA sequence analysis revealed a novel homozygous mutati
217 ence for cooperativity among the SARs, while
DNA sequence analysis revealed a series of clustered A-t
218 DNA sequence analysis revealed a single missense mutatio
219 DNA sequence analysis revealed a single point mutation c
220 DNA sequence analysis revealed changes in c.545A>G, c.13
221 DNA sequence analysis revealed dominant T cell clones ob
222 DNA sequence analysis revealed multiple nucleotide subst
223 DNA sequence analysis revealed potential transcriptional
224 DNA sequence analysis revealed several widely distribute
225 DNA sequence analysis revealed that 18 isolates containe
226 DNA sequence analysis revealed that CAP60 has similarity
227 DNA sequence analysis revealed that EUs4 of the pathogen
228 DNA sequence analysis revealed that in both 91-R and ry5
229 DNA sequence analysis revealed that in six of nine delet
230 DNA sequence analysis revealed that M. smegmatis does in
231 wly synthesized strand followed by multiplex
DNA sequence analysis revealed that mutation fixation at
232 DNA sequence analysis revealed that the B3 genome is 38,
233 DNA sequence analysis revealed that the chromosomal inse
234 DNA sequence analysis revealed that the complementing ac
235 DNA sequence analysis revealed that the donor clone pred
236 DNA sequence analysis revealed that the KnR cassette was
237 DNA sequence analysis revealed that the majority of the
238 DNA sequence analysis revealed that the putative yhdJ DN
239 DNA sequence analysis revealed that the transposon inser
240 DNA sequence analysis revealed that there are several ka
241 However,
DNA sequence analysis revealed that these were independe
242 DNA sequence analysis revealed that this clone contains
243 Subcloning, transposon mutagenesis, and
DNA sequence analysis revealed that this DNA fragment co
244 DNA sequence analysis revealed that this locus is simila
245 Subsequent cloning and
DNA sequence analysis revealed that transposon insertion
246 DNA sequence analysis revealed that two of the novel HAB
247 DNA sequence analysis revealed the mutation to be a sing
248 DNA sequence analysis revealed the nature of the cer6-1,
249 DNA sequence analysis revealed the presence of multiple
250 DNA sequence analysis revealed three open reading frames
251 The
DNA sequence analysis revealed two consecutive open read
252 DNA sequence analysis revealed two xenobiotic response e
253 DNA sequencing analysis revealed target-dependent mutati
254 DNA sequence analysis reveals a proteobacterial architec
255 Genomic
DNA sequence analysis reveals that JMRV is a gammaherpes
256 However,
DNA sequence analysis reveals that, with the exception o
257 DNA sequence analysis showed 93% identify with the rat e
258 DNA sequence analysis showed considerable divergence bet
259 PCR and
DNA sequence analysis showed extensive genotypic diversi
260 DNA sequence analysis showed normal sequence for GPIbalp
261 DNA sequence analysis showed that ORF2 extended an addit
262 DNA sequence analysis showed that the affected individua
263 DNA sequence analysis showed that the frequency of in-fr
264 o human IKCa1 cDNA probes were isolated, and
DNA sequence analysis showed that they were identical to
265 DNA sequence analysis shows that the methylated componen
266 DNA sequence analysis suggested that dev and cas (CRISPR
267 This
DNA sequence analysis suggested that the terminal defici
268 depending on the strain, was identified, and
DNA sequence analysis suggests that horizontal gene tran
269 We developed a new approach to
DNA sequence analysis that uses fluorogenic reporter mol
270 Based on
DNA sequence analysis,
the three genes are likely to be
271 We tested the use of comparative
DNA sequence analysis to aid identification of promoter
272 , all the cases of hereditary TTP studied by
DNA sequence analysis to date appear to be due to mutati
273 The SQ-PCR Av assay was verified using
DNA sequence analysis to demonstrate that this methodolo
274 followed by Southern blot hybridisation and
DNA sequence analysis to detect DNAs of polyomaviruses a
275 We used
DNA sequence analysis to determine that the element harb
276 ed by oligodeoxynucleotide hybridization and
DNA sequence analysis to establish the mutation frequenc
277 r-based genome scanning, marker sorting, and
DNA sequence analysis to examine their phylogenetic rela
278 mpling and a microbiopsy device coupled with
DNA sequence analysis to highlight BRAF V600E heterogene
279 nd GyrB subunits of DNA gyrase, we have used
DNA sequence analysis to identify a highly conserved 'Gy
280 -strand conformation polymorphism (SSCP) and
DNA sequence analysis to identify mutations in the cardi
281 Combining microarray techniques with
DNA sequence analysis to identify potential let-7 target
282 Here, we describe a multigenomic
DNA sequence-analysis tool, evoprinter, that facilitates
283 nterconnection of the ECR Browser with other
DNA sequence analysis tools creates a unique portal for
284 For some isolates,
DNA sequence analysis was also performed.
285 pparent pathologic mutations in these genes,
DNA sequence analysis was performed of a candidate OCA g
286 mission distortion of the marker alleles and
DNA sequence analysis was performed.
287 DNA sequence analysis was used to show that the combinat
288 Based on
DNA sequence analysis we propose that GGPPS5 (At3g14510)
289 Using direct
DNA sequencing analysis,
we screened 13 genes for mutati
290 ll disagreements with conventional gel-based
DNA sequence analysis were confirmed by re-analysis with
291 Methods of
DNA sequence analysis were employed to scan herpesvirus
292 PCR-based assays and
DNA sequence analysis were performed for these 34 loci i
293 PCR and
DNA sequence analysis were used to characterize the alte
294 DNA extraction, rpoB gene amplification, and
DNA sequencing analysis were performed.
295 y direct fluorescent antibody test (DFA) and
DNA sequencing analysis were tested.
296 Analysis of the mutant strains by
DNA sequence analysis,
Western blot assays, and reconstr
297 results lead us to conclude that comparative
DNA sequence analysis will enable identification of func
298 DNA sequence analysis with other vertebrate Rb sequences
299 d by the molecular approach (PCR followed by
DNA sequencing analysis)
with those from the parasitolog
300 ovel transmembrane protein was identified by
DNA sequence analysis within the insulin-dependent diabe