ライフサイエンスコーパス: DNA fragment

1 scription initiation complex with a promoter DNA fragment.

2 a lower concentration to amplify its target DNA fragment.

3 and multiple copies of that gene are on one DNA fragment.

4 onal 270 bp DNA fragment and lacked a 450 bp DNA fragment.

5 apter oligonucleotides are hybridized to the DNA fragment.

6 samples containing small organic anions and DNA fragment.

7 vs. 11/20 aqueous samples along with shorter DNA fragments.

8 elective amplification of minute quantity of DNA fragments.

9 target at its center to generate blunt-ended DNA fragments.

10 d on micrometre scale for megabasepair-sized DNA fragments.

11 8 in complex with several origin of transfer DNA fragments.

12 ulti-gene circuitry assembled from different DNA fragments.

13 CHD4 interacts with PAX3-FOXO1 via short DNA fragments.

14 hat often require screening large numbers of DNA fragments.

15 mple droplets containing fluorescent dyes or DNA fragments.

16 he sequencing-adapters and the length of the DNA fragments.

17 as a single-base-pair change to insertion of DNA fragments.

18 aptamer was enzymatically cleaved into short DNA fragments.

19 thods for the detection of sequence-specific DNA fragments.

20 we find Hha improves H-NS binding to target DNA fragments.

21 vertices within a network of double-helical DNA fragments.

22 in a chiral liquid crystal containing short DNA fragments.

23 rom samples that are enriched for methylated DNA fragments.

24 to pry polymerase from incompletely extended DNA fragments.

25 that was more apparent on particular genomic DNA fragments.

26 rom samples that are enriched for methylated DNA fragments.

27 rhang but not of 5' overhangs or blunt-ended DNA fragments.

28 gregation process in a system containing 458 DNA fragments.

29 tiple and often large (up to at least 44 kb) DNA fragments.

30 e G-quadruplex targets have often been short DNA fragments.

31 lytic 3' -> 5' degradation of the individual DNA fragments.

32 ing undocumented cassettes and contaminating DNA fragments.

33 a preference for short (17- to 19-base-pair) DNA fragments.

34 orm thermal control for the amplification of DNA fragments.

35 of more than 8 million 20- to 300-kb genomic DNA fragments.

36 bp) and of 23S rDNA A2143G results in three DNA fragments (108, 310 and 350pb), due to a conserved B

37 RSE) is characterized by the capture of long DNA fragments (15-20 kb) by magnetic beads, after enzyma

38 27 and 37 bp) and its absence originated two DNA fragments (264 and 281 bp) due to a 16 S rDNA conser

39 cient non-mosaic targeted insertion of small DNA fragments (40-50 nucleotides) in 4.4-25.7% of F0 tad

40 Occurrence of 23S rDNA A2142G results in two DNA fragments (418 and 350 bp) and of 23S rDNA A2143G re

41 cally unfold structures in a human telomeric DNA fragment, 5'-(TTAGGG)4TTA, along three different tra

42 developed for detection of an avian-specific DNA fragment (68bp) in farm animal and pet feeds.

43 , FragSeq, and apply this method to identify DNA fragments accumulated in Escherichia coli cells unde

44 It can not only bin DNA fragments accurately at a species level but also at

45 orphology and oligonucleosomal double-strand DNA fragments (also known as DNA ladder) are considered

46 EMAST was detected by DNA fragment analysis.

47 tructures and melting points of the chimeric DNA fragment and its complexes with perfect-matched and

48 xposed snails exhibited an additional 270 bp DNA fragment and lacked a 450 bp DNA fragment.

49 of Mg(2+) to release the fluorophore-labeled DNA fragment and produce a fluorescent turn-on signal fo

50 s, microfluidic partitioning of long genomic DNA fragments and barcoding of shorter fragments derived

51 It also assembled multiple DNA fragments and did simultaneous site-directed mutagen

52 ethods: umbrella sampling simulations of two DNA fragments and direct observation of the aggregation

53 accommodates parallel nicking on orthogonal DNA fragments and enzymatic toehold creation that enable

54 chnique was tested on complexes of two model DNA fragments and four ligands, namely, a representative

55 we demonstrate that TOP-PCR recovers minute DNA fragments and maintains the DNA size profile, while

56 e, and high-throughput method to internalize DNA fragments and proteins labeled with organic fluoroph

57 d pure hybrids free of polydisperse digested DNA fragments and serum biomolecules.

58 Upon capture, the noncomplementary DNA fragments and serum constituents of varying sizes we

59 EXO1), play a major role in generating these DNA fragments and that the cytoplasmic 3'-5' exonuclease

60 DNA samples between the number of surviving DNA fragments and their length, ancient DNA sequencing l

61 " read duplicates that represent independent DNA fragments and therefore, over-estimate the PCR dupli

62 , a dye is used to intercalate the amplified DNA fragments, and identifications of the pathogens are

63 lysis of incompetent streptococci, uptake of DNA fragments, and integration of strands of that DNA in

64 med the binding of YY1 to unprocessed let-7a DNA fragments, and treatment with YY1 shRNA increased le

65 al cell/glycocalyx damage (histone-complexed DNA fragments, annexin V, thrombomodulin, syndecan-1), p

66 easing the rate at which externally supplied DNA fragments are incorporated into the genome through h

67 cation of this recovery method, biotinylated DNA fragments are isolated from a mixed solution to prov

68 gments with a length between 140 and 180 bp) DNA fragments are recovered and sequenced on Illumina Hi

69 Biotin-containing genomic DNA fragments are then enriched using streptavidin beads

70 e-5-methylenesulfonate (CMS); CMS-containing DNA fragments are then immunoprecipitated using a CMS-sp

71 s that genomic sequencing coverage of plasma DNA fragments around transcription start sites reflects

72 on/renaturation were used to amplify protein DNA fragments as confirmed by DNA sequencing.

73 demonstrate a convenient rapid procedure for DNA fragment assembly using site-specific recombination

74 Sequencing DNA fragments associated with proteins following in vivo

75 btilis in complex with a 12 base palindromic DNA fragment at a resolution of 3.2 A.

76 Target DNA fragments at 10 fM concentration (approximately 6 x

77 wn strategy enables the isolation of genomic DNA fragments bearing single, as well as multiple G-quad

78 PARPi promoted accumulation of cytosolic DNA fragments because of unresolved DNA lesions, which i

79 gh a novel mechanism of insertion of a large DNA fragment between the V and DJ segments.

80 e report that, despite the large size of the DNA fragment, both plasmid integration and duplication r

81 whether specific sequences were enriched in DNA fragments bound by TLS.

82 and on the inversion of a central 32-kb-long DNA fragment, but overall their genomes displayed a high

83 esulted from local amplification of a 134-bp DNA fragment by the mat1-switching phenomenon.

84 ication of the target deoxyribonucleic acid (DNA) fragments by using single-nucleotide-polymorphism p

85 In Drosophila, PcG proteins are bound to DNA fragments called Polycomb group response elements (P

86 The flexibility of a DNA fragment can be experimentally and computationally e

87 rapping patterned cells inside gels, damaged DNA fragment can diffuse out of the nucleus and form a h

88 Because DNA fragments can increase arthritis severity in preclin

89 oach is also able to distinguish between two DNA fragments carrying both N6-methyladenine and 5-methy

90 library construction methods that enrich for DNA fragments carrying deaminated cytosine residues, we

91 CC-seq signal reveals regional enrichment of DNA fragments characteristic of alternating rather than

92 A natural competence based large DNA fragment cloning (NabLC) technique was developed, wh

93 this hairpin formation or the addition of a DNA fragment complementary to the hairpin destroys the c

94 ed structural signature of the 180-base pair DNA fragment comprising the homeobox.

95 In Golden Transformation, linear DNA fragments constructed by Golden Gate Assembly are di

96 1 or its isolated CID domain to a methylated DNA fragment containing alternating purine/pyrimidines,

97 However, the DNA fragment containing the associated SNPs interacts th

98 MYB112 binds to an 8-bp DNA fragment containing the core sequence (A/T/G)(A/C)CC

99 switch was due to the exchange of a 35.5-kb DNA fragment containing the entire cps operon.

100 eavage of a UG duplex generates the expected DNA fragments containing a 5'-terminal deoxyuridine mono

101 stranded DNA substrates to generate unhooked DNA fragments containing either an abasic site or a psor

102 viously showed that both linear and circular DNA fragments containing the 2-LTR palindrome junction c

103 rough ultrathin solid-state nanopores, short DNA fragments containing thymine modifications were foun

104 lus RNA polymerase, sigma(A), and a promoter DNA fragment corresponding to the transcription bubble a

105 DNA fragments covering these regulatory elements were am

106 we used to simultaneously assess over 80,000 DNA fragments derived from nucleosome-free regions withi

107 DNA fragments derived from the 5' region of SLC26A9-bear

108 ing in vitro on four plasmid DNAs containing DNA fragments derived from the genomes of sheep, drosoph

109 ication (oriLyt) in order to synthesize long DNA fragments during replication.

110 h the cleavage sites that generate the 50 kb DNA fragments during the first stages of programmed cell

111 is also involved in the generation of small DNA fragments during the repair of high LET radiation-in

112 ion, we show that insertion of mitochondrial DNA fragments during the repair of induced double-strand

113 (SuRE), a method that assays more than 10(8) DNA fragments, each 0.2-2 kb in size, for their ability

114 ation, we combined CRISPR/Cas9-based genomic-DNA-fragment editing with chromosome-conformation-captur

115 molecular enrichment for promoter-containing DNA fragments enables the systematic mapping of interact

116 is-tagged CouR bound with high affinity to a DNA fragment encompassing the couAB promoter region, and

117 ke the probability of placement, the size of DNA fragments enriched for nucleosomes and/or whether nu

118 nal deep sequencing of short single-stranded DNA fragments enriched for RNA-primed nascent strands is

119 nsferase-mediated dUTP nick-end labeling and DNA fragment enzyme-linked immunosorbent assay.

120 tide variations generated by uptake of short DNA fragments escape mismatch repair.

121 18S-ITS-5.8S, 28S D2/D3 and a mitochondrial DNA fragment flanking cytochrome oxidase gene subunit II

122 Why human telomere DNA fragments fold into different G-quadruplex structure

123 These DNA fragments fold into G-quadruplex structures and when

124 caspases in tumor cells to produce abundant DNA fragments for DNA sensing in antigen-presenting cell

125 based tool, that automates the generation of DNA fragments for integration.

126 eactions using these nucleotides to generate DNA fragments for MALDI-TOF MS analysis.

127 lpha/primase complex assembles the short RNA-DNA fragments for priming of lagging and leading strand

128 nce allows bacteria to internalize exogenous DNA fragments for the acquisition of new phenotypes such

129 This DNA fragment formed a stable two G-tetrad antiparallel G

130 rand-specific, high-throughput sequencing of DNA fragments, FragSeq, and apply this method to identif

131 present the discovery of a 36-kilo-base pair DNA fragment from Vibrio splendidus encoding enzymes for

132 ata of three nuclear genes and three plastid DNA fragments from 109 accessions of Avena L.

133 -fold and recover an average of 96.4% of the DNA fragments from 2.0 to 23 kbp uniformly.

134 previously identified in silico evidence of DNA fragments from a Pseudomonas-like bacteria integrati

135 , we describe an advanced system for joining DNA fragments from a universal library that automaticall

136 enomic DNA libraries, we are able to capture DNA fragments from across the human genome.

137 y a purifying step for receiving amplifiable DNA fragments from bacteria in less than 25 min.

138 nes to amplify 172, 163, 141, 129 and 108 bp DNA fragments from cat, dog, pig, monkey and rat meats,

139 rom regions where either genome has acquired DNA fragments from diverged genomes by homologous recomb

140 The assay amplified specific DNA fragments from dog (230 bp), duck (283 bp), buffalo

141 reSelect and NimbleGen's SeqCap, to generate DNA fragments from genomic target regions.

142 roughput functional selection to isolate ten DNA fragments from human oral and fecal metagenomes that

143 CRISPR-Cas adaptive immune systems capture DNA fragments from invading bacteriophages and plasmids

144 preparation protocols to better retain short DNA fragments from plasma, and applied these optimized m

145 n improved method for the isolation of small DNA fragments from serum using selective precipitation b

146 In addition, we identify DNA fragments from several bacterial and viral taxa, inc

147 to provide high-confidence identification of DNA fragments from uncultivated members of the Roseobact

148 se results demonstrate that TLR9 responds to DNA fragments generated by DNase II.

149 gargammel, a package that simulates ancient DNA fragments given a set of known reference genomes.

150 Since the size range of sheared virus DNA fragments governs the limit of accurate protein loca

151 for integrating optical mapping (OM) of long DNA fragments (>150 kb) with next-generation sequencing

152 Recombination of large DNA fragments (>30 kb), sometimes including the capsular

153 is a truncated form of the genome into which DNA fragments harboring the structural genes are ligated

154 cient products allowing assembly of multiple DNA fragments have become available.

155 tect very low levels (0.01 ng/ml) of a small DNA fragment in serum.

156 verlap sequences, we can assemble up to five DNA fragments in a defined order and insert them into a

157 hich allows the detection of less than 10000 DNA fragments in a sample of 100 muL (corresponding to ~

158 Poisson statistics to estimate the number of DNA fragments in a sample with a specific sequence.

159 hat helps determine the size distribution of DNA fragments in an NGS library, or other DNA sample, ba

160 The size of the "invisible" DNA fragments in botanical extracts was around 20-220bp

161 ed were all intronic T-DNA mutants and the T-DNA fragments in both the trigger T-DNA as well as in th

162 ent for Sequence Analysis), isolates genomic DNA fragments in microfluidic droplets and performs TaqM

163 ful because they enable assembly of multiple DNA fragments in one reaction, at the cost of requiring

164 s the highly selective extraction of desired DNA fragments in order to minimize interferences from sa

165 developed an approach to identify rearranged DNA fragments in sera, providing personalized biomarkers

166 lack of Trex2 results in the accumulation of DNA fragments in the cytoplasm of cornifying lingual ker

167 uid biopsy analysis of circulating cell-free DNA fragments in the patients' blood can monitor clonali

168 us behavior of the double helix happens when DNA fragments in the range of 100 bp are circularized wi

169 a (fetal bovine serum) and other interfering DNA fragments in the range of 50-1500 base pairs.

170 NII is fully embedded in CP, we inserted HBV DNA fragments in the sense orientation to determine thei

171 mbinants had received multiple donor-derived DNA fragments in the size range of 100 bp to 118 kbp, fr

172 entists have observed small extrachromosomal DNA fragments in tumor cells, yet comprehensive examinat

173 leosome architecture, via analysis of larger DNA fragments, in a single assay.

174 cloning approaches use in vitro assembly of DNA fragments, in vivo cloning offers potential for grea

175 omes, FRET observed upon H1 binding to naked DNA fragments includes both intra- and inter-molecular r

176 Moreover, replacing 3'RR with a DNA fragment including only its four DNase I hypersensit

177 ials of mean force between the H4 tail and a DNA fragment indicate that contrary to the expectations

178 DNA identified a peak at 145 bp in the human DNA fragments, indicating a difference in the origin or

179 is highly correlated with the length of the DNA fragments, indicating that the sizes of PCR products

180 (over 14%) of random plasmid or chromosomal DNA fragment insertion at the target sites in transgenic

181 hat restriction did not affect the length of DNA fragment integration during natural transformation.

182 restrictive, in that they packaged only one DNA fragment into the head, whereas motors with the 120-

183 ocess that joins discontinuously synthesized DNA fragments into a contiguous lagging strand.

184 tegrase associates with Cas2 to insert short DNA fragments into a CRISPR array, establishing nucleic

185 s by insertion of foreign (viral or plasmid) DNA fragments into clustered regularly interspaced short

186 neous end-to-end association of short duplex DNA fragments into long rod-like structures.

187 ocation involves the integration of inactive DNA fragments into nuclear chromosomes, and this process

188 bacterial cell extracts to assemble multiple DNA fragments into recombinant DNA molecules in a single

189 grase to capture and integrate short foreign DNA fragments into the CRISPR locus, enabling adaptation

190 unity requires integration of short, foreign DNA fragments into the host genome at the CRISPR locus,

191 Generated through the random integration of DNA fragments into the host genome, transgenesis can lea

192 utions of monodisperse stiff double-stranded DNA fragments is known not to occur, despite the fact th

193 presence of present-day human contaminating DNA fragments is one of the challenges defining ancient

194 The retention of DNA fragments is strongly influenced by both their proxi

195 However, DNA fragments isolated from ancient specimens show a cha

196 whereas reptation-based transport occurs for DNA fragments larger than 500 base pairs.

197 ieval, amplification and sequencing of trace DNA fragments left behind by marine organisms; an approa

198 DNA fragment length and TaqMan assays were used to genot

199 ch which moves computational complexity from DNA fragment length to fragment overlap, i.e., coverage,

200 ), we observe a highly structured pattern of DNA fragment lengths and positions around nucleosomes in

201 ndependent resource for automatic scoring of DNA fragment lengths diversity panels and biparental pop

202 The program analyzes DNA fragment lengths generated in Applied Biosystems(R)

203 ue to high rates of nucleotide damage, short DNA fragment lengths, low endogenous DNA content and the

204 To test this hypothesis, BoHV-1 DNA fragments (less than 400 bp) containing potential GR

205 Intergenic viral DNA fragments (less than 400 bp) containing two GREs and

206 equences have diverged to a degree that most DNA fragments longer than 50 bp are unique to just one s

207 ffect is attributable, in part, to the small DNA fragments (</=40 bp) directly produced by high LET r

208 urred at low frequency with relatively small DNA fragments (<1.8 kb).

209 measurements accomplished using non-specific DNA fragments mixed with samples, revealed the high spec

210 The target DNA fragment of 18s rRNA gene was amplified and hybridiz

211 ion pathway are located in a 25.2-kb genomic DNA fragment of CBB1, including cdhABC (coding for caffe

212 An interaction study of the C-dots and the DNA fragment of lambda bacteriophage was performed, and

213 A 354-bp DNA fragment of VP1, an effective marker for diagnosing

214 Five promoter-reporter constructs containing DNA fragments of 0.74kb, 1.35kb, 1.84kb, 3.97kb and 4.76

215 Given a set of DNA fragments of an individual, it consists of determini

216 med by simultaneously deleting and inserting DNA fragments of different sizes at a common genomic loc

217 LAMP amplification for 0.18 kbp and 0.23 kbp DNA fragments of femB and mecA genes, respectively.

218 ent on various preparative steps to generate DNA fragments of required concentration, purity and aver

219 were obtained with noncomplementary, control DNA fragments of similar length.

220 on and partitioning of large single-stranded DNA fragments of the homologous chromosome pairs allows

221 Among the systems considered are a large DNA fragment, oligopeptides, and even entire proteins in

222 unction, a multitude of genes, and noncoding DNA fragments or on a number of lengthy sequence-typing

223 This method is nondestructive, preserving DNA fragments over 10 kilobases long.

224 The mononucleosome-sized DNA fragments precisely define genome-wide nucleosome po

225 ing a Poisson distribution for the number of DNA fragments present in each chamber, the DNA concentra

226 r (double-digest restriction site-associated DNA fragment procedure [ddRAD]) and mitochondrial DNA se

227 single cells, while the subnucleosome-sized DNA fragments provide information on chromatin accessibi

228 ch as transcriptomics, the millions of short DNA fragments (reads) produced by current sequencing pla

229 meters yield very similar results for longer DNA fragments, regardless of the nucleotide sequence, wh

230 16 S rDNA TetR genotype resulted in a three DNA fragment restriction pattern (281, 227 and 37 bp) an

231 ow tumor fraction (TF) and limited number of DNA fragments restricts low-disease-burden monitoring th

232 Sensing of these DNA fragments results in pyroptosis, a highly inflammato

233 The metagenomic Roseobacter DNA fragments revealed several traits with evolutionary

234 However, for DNA fragments shorter than 100 bp, all sets of parameter

235 s the simultaneous sequencing of billions of DNA fragments simultaneously, has revolutionized how we

236 at these high-resolution measurements of CMV DNA fragment size accurately predict measured discrepanc

237 Further, the effects of the DNA fragment size on aggregation was explored, where lar

238 l conditions, Ogston sieving is achieved for DNA fragments smaller than 500 base pairs, whereas repta

239 , Pyrococcus furiosus, actively incorporates DNA fragments (spacers) from both plasmid (foreign) and

240 HIV-1 subgenomic DNA fragments, spanning the long terminal repeats and th

241 ecule imaging with DNA chains assembled from DNA fragments such that a chain is labeled at designated

242 rticularly useful for inserting heterologous DNA fragments, such as GFP, into a specific genomic locu

243 this study, structural changes of 22-mer ht-DNA fragment (Tel22), induced by binding of ions (K(+),

244 volves adaptation, the integration of ~30-bp DNA fragments, termed prespacers, into the CRISPR array

245 rpin and a G-quadruplex in a single-stranded DNA fragment that is found in the promoter region of hum

246 telomere dysfunction and cytosolic telomeric DNA fragments that are sensed by cGAS.

247 ion score-which allows the identification of DNA fragments that are unlikely to originate from presen

248 talyzed by active transposases, can generate DNA fragments that are used by the CRISPR-Cas adaptation

249 uencing, to identify B. subtilis chromosomal DNA fragments that bind CodY in vitro.

250 tes as low as 10(-8) and average 500-kb-long DNA fragments that can be assembled into haplotype conti

251 ng methods have limitations on the number of DNA fragments that can be simultaneously manipulated, wh

252 lation of a cleavable linker between the two DNA fragments that comprise the sensor.

253 without considering the transposase digested DNA fragments that contain additional nucleosome positio

254 h as the precise insertion or replacement of DNA fragments that contain the coding regions of genes.

255 Additionally, five genomic islands, e.g. DNA fragments that facilitate horizontal gene transfer p

256 nsic cyclizabilities of 270,806 50-base-pair DNA fragments that span Saccharomyces cerevisiae chromos

257 gile nucleosomes were defined by nucleosomal DNA fragments that were recovered preferentially in earl

258 sidering that just after dissociating from a DNA fragment the protein remains in close proximity to t

259 ifications, translocations and inversions of DNA fragments thereby modifying genome architecture, and

260 1L2 and Trex2 causes massive accumulation of DNA fragments throughout the cornified layers of the ton

261 Ecl18kI, interacts with a FRET pair-labeled DNA fragment to form two different DNA loop conformation

262 Because the selective physical adsorption of DNA fragments to gold enable a direct read-out of region

263 d repairing DNA template flanked by homology DNA fragments to the target site, were demonstrated to g

264 ncer and promoter activities of thousands of DNA fragments transduced into mouse neurons.

265 rmination of microsatellite lengths or other DNA fragment types is an important initial component of

266 bLC) technique was developed, which can move DNA fragments up to 40-kb directly and integrate a 73.7-

267 Large genomic DNA fragment (up to 95 kb) deletion mice were generated

268 ovalently tag and sequence uracil-containing DNA fragments (UPD-Seq).

269 Furthermore, all three proteins bind to a DNA fragment upstream of the bmp2b transcription start s

270 A DNA fragment upstream of the dev promoter was bound by a

271 bes strategically located on the interacting DNA fragments used for recombination.

272 ll lines: targeted cleavage of mitochondrial DNA fragments using CRISPR technology and removal of det

273 that enable the efficient assembly of linear DNA fragments, using reactions developed by Gibson for t

274 The transgene DNA fragment was unmethylated before it was injected int

275 In contrast, integration of random DNA fragments was not observed in transgenic events gene

276 single molecule mapping of telomere-terminal DNA fragments, we provide proof of principle for a novel

277 Using this method on linear DNA fragments, we show empirically that the requirements

278 ] and mitochondrial DNA [mtDNA]) and nuclear DNA fragments were measured in plasma from APAP-overdose

279 encies of receipt and donation of recombined DNA fragments were observed in non-encapsulated lineages

280 us detections of four conserved HIV-1 B-type DNA fragments were performed in this integrated microflu

281 l ndm genes are located in a 13.2-kb genomic DNA fragment which also contained a formaldehyde dehydro

282 resent a multiplex microarray-based assay of DNA fragments, which allows the detection of less than 1

283 uble-strand breaks (DSBs) that include small DNA fragments, which are not repaired by the non-homolog

284 e-elicited double-strand DNA breaks releases DNA fragments, which may either activate the cGAS/STING-

285 ure of S1-15 in complex with single-stranded DNA fragments, which may provide clues about the genesis

286 of stable RNAP complexes with model promoter DNA fragments whose downstream ends extend from +3 to +2

287 at provide a drag equivalent to an uncharged DNA fragment with a length (alpha) of 509 bases (effecti

288 ngle-stranded overhangs, if present, on each DNA fragment with an overall accuracy between 80-90%.

289 The DNA fragment with the top-associated SNP 27:19,086,778 d

290 ) blocks end-joining of double-stranded (ds) DNA fragments with 3' overhangs mimicking double-strand

291 nsor has the ability to detect complementary DNA fragments with a detection limit down to 20 DNA targ

292 We show that competent V. cholerae acquire DNA fragments with a length exceeding 150 kbp in a T6SS-

293 l the expression of mouse non-coding genomic DNA fragments with enhancer activity.

294 at pulldown efficiency sharply increases for DNA fragments with four or more mCpGs.

295 The assembly of DNA fragments with homologous arms is becoming popular i

296 verage with two signals: The first considers DNA fragments with only a single binding event, whereas

297 DNA fragments with short homologous ends were treated by

298 ntial chain-reaction generating biotinylated DNA fragments within minutes.

299 Single-insert cloning of DNA fragments without restriction enzymes has traditiona

300 in an average of 11.5 fold increase in short DNA fragments yield (DNA <100bp).