ライフサイエンスコーパス: DNA fragment

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

2 ection of DNA, including a hepatitis B virus DNA fragment.

3 ich can further capture another protein-free DNA fragment.

4 unless both modified bases occur in the same DNA fragment.

5 d induce homologous recombination of a donor DNA fragment.

6 chain reaction (PCR) for an influenza viral DNA fragment.

7 scription initiation complex with a promoter DNA fragment.

8 a lower concentration to amplify its target DNA fragment.

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

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

11 aptamer was enzymatically cleaved into short DNA fragments.

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

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

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

15 in a chiral liquid crystal containing short DNA fragments.

16 rom samples that are enriched for methylated DNA fragments.

17 to pry polymerase from incompletely extended DNA fragments.

18 that was more apparent on particular genomic DNA fragments.

19 rom samples that are enriched for methylated DNA fragments.

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

21 gregation process in a system containing 458 DNA fragments.

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

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

24 n of Spo11 protein covalently bound to small DNA fragments.

25 nucleosomes to extreme end positions on the DNA fragments.

26 first time PBD adducts with single-stranded DNA fragments.

27 igh-throughput cloning of single or multiple DNA fragments.

28 tical for centering mononucleosomes on short DNA fragments.

29 elective amplification of minute quantity of DNA fragments.

30 e chromosomes by dynamically linking distant DNA fragments.

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

32 ultiple cognate sites on 100- to 300-kb-long DNA fragments.

33 to the Abl interactor 1, SHP-1, and nuclear DNA fragments.

34 tants were normal in unwinding linear origin DNA fragments.

35 d to the analysis of j-factors of very short DNA fragments.

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

37 8 in complex with several origin of transfer DNA fragments.

38 ulti-gene circuitry assembled from different DNA fragments.

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

40 hat often require screening large numbers of DNA fragments.

41 mple droplets containing fluorescent dyes or DNA fragments.

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

43 27 and 37 bp) and its absence originated two DNA fragments (264 and 281 bp) due to a 16 S rDNA conser

44 o methylated Illumina adapters, the CpG-rich DNA fragments (40-220 bp) are size selected, subjected t

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

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

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

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

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

50 EMAST was detected by DNA fragment analysis.

51 virus by 6.5- to 200-fold, depending on the DNA fragment analyzed, thus indicating a profound defect

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

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

54 e describing the interaction between a short DNA fragment and topo IB.

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

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

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

58 echniques for detection of microbial genomic DNA fragments and opens up new possibilities for the ult

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

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

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

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

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

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

65 o induce homologous recombination of a donor DNA fragment, and report the quantification of the frequ

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

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

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

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

70 Notably, the transcription of these miRNA DNA fragments appears resistant to conventional inhibito

71 Individual DNA fragments are amplified and analyzed either by flow

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

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

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

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

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

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

78 Sequencing DNA fragments associated with proteins following in vivo

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

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

81 as based on measuring the j-factors of short DNA fragments at various temperatures.

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

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

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

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

86 phoresis (FSCE), a drag-tag attached to each DNA fragment breaks linear charge-to-friction scaling, e

87 lows affinity enrichment of 5-hmC-containing DNA fragments but also enhances the kinetic signal of 5-

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

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

90 formation when it was bound to nixA and ureA DNA fragments by tethering (S)-1{[bis(carboxymethyl)amin

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

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

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

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

95 Because DNA fragments can increase arthritis severity in preclin

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

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

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

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

100 UNG was incubated with a 30 bp DNA fragment containing a single uracil, giving the comp

101 1 or its isolated CID domain to a methylated DNA fragment containing alternating purine/pyrimidines,

102 AP), RNA polymerase holoenzyme (RNAP), and a DNA fragment containing positions -78 to +20 of a Class

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

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

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

106 DBD was able to specifically bind to a short DNA fragment containing the fnbA promoter, suggesting th

107 Stepwise addition of a DNA fragment containing the kappaB binding sequence to t

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

109 Using DNA fragments containing a MC-mono-dG or an ICL dG-MC-dG

110 n of enzymatic and chemical steps to isolate DNA fragments containing as few as a single 5hmC.

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

112 zymes is that they are able to extract small DNA fragments containing modified sites on genomic DNA,

113 Genomic DNA fragments containing only the DNJ1 gene encoding a t

114 omotor region of DEXI but not with candidate DNA fragments containing other potential causal genes in

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

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

117 DNA fragments covering these regulatory elements were am

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

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

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

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

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

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

124 We prepared DNA fragments, each about 200 bp in length, with various

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

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

127 ession of a luciferase reporter plasmid, the DNA fragment encompassing the 3-bp deletion polymorphism

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

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

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

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

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

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

134 ows one-step cloning of up to four gene-size DNA fragments, followed by a second assembly of these co

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

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

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

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

139 rigin binding domain (OBD) in complex with a DNA fragment from the MCV origin of replication.

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

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

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

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

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

145 ctive strategy for directional subcloning of DNA fragments from Bacteria Artificial Chromosomes (BACs

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

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

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

149 Plasmids harboring these genomic DNA fragments from F. johnsoniae promoted strong product

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

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

152 knock out (KO) and pull out (PO) chromosomal DNA fragments from naturally transformable Burkholderia

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

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

155 (BAC) vectors enable stable cloning of large DNA fragments from single genomes or microbial assemblag

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

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

158 nstrate that deep sequencing of the digested DNA fragments generated from these enzymes provides a fe

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

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

161 However, the ability to carry DNA fragments >10 kb is limited in most DNA transposons.

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

163 shearing, adapter ligation, and selection of DNA fragments harboring Mu flanking sequences by hybridi

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

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

166 he GAL1 promoter, and the URA3 marker) and a DNA fragment homologous to the sequence upstream of the

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

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

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

170 teracting transcription factors for multiple DNA fragments in a short time.

171 drodynamically separate a wide size range of DNA fragments in a single run without the need for gels,

172 ies for the ultrasensitive quantification of DNA fragments in a wide variety of application areas usi

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

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

175 nrichment and sequencing of 5-hmC-containing DNA fragments in mammalian genomes.

176 t allow the stable delivery of large genomic DNA fragments in mammalian systems is important for gene

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

178 DNA transposon piggyBac can mobilize 100-kb DNA fragments in mouse embryonic stem (ES) cells, making

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

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

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

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

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

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

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

186 Mre11 and Ku respond differently to shorter DNA fragments in vitro and to the DNA from high-LET irra

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

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

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

190 that, in the absence of exogenous promoters, DNA fragments incorporating miRNA precursors can be deli

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

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

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

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

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

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

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

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

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

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

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

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

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

204 To assemble the wires, DNA fragments labeled with a series of increasingly red-

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

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

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

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

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

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

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

212 A long DNA fragment library is converted to a population of nes

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

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

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

216 regulatory networks, however, large sets of DNA fragments need to be processed at high throughput an

217 It is the GC content of the full DNA fragment, not only the sequenced read, that most inf

218 e have recently shown that in fully solvated DNA fragments, nucleobases are particularly attractive f

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

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

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

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

223 eDNA contains DNA fragments of a size that has the potential to transf

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

225 In this study, we sequenced complementary DNA fragments of cultured human B-cells and obtained 879

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

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

228 The DNA fragments of identical length can also be generated

229 sites, which can be used to produce a set of DNA fragments of identical length to study protein-induc

230 erful tool for unidirectional integration of DNA fragments of interest into a pre-determined genome l

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

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

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

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

235 wild-type FlhD(4)C(2)-protected fragment and DNA fragments possessing mutations in one section of the

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

237 udy reports the successful detection of long DNA fragments produced by PCR following extraction from

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

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

240 ial gyrase complexes bound to 137- or 217-bp DNA fragments representing the starting conformational s

241 16 S rDNA TetR genotype resulted in a three DNA fragment restriction pattern (281, 227 and 37 bp) an

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

243 The metagenomic Roseobacter DNA fragments revealed several traits with evolutionary

244 ues to show that PRH oligomers bound to long DNA fragments self-associate to form highly ordered asse

245 s for DNA extraction, PCR amplification, and DNA fragment separation, including the more conventional

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

247 Sequence analysis of trapped DNA fragments showed conserved Bacteroidetes promoter mo

248 Among these markers, DNA fragment size has shown promise for discerning the s

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

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

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

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

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

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

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

256 isolated and characterized a 2.8 kb genomic DNA fragment that regulates expression of Rax in the dev

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

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

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

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

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

262 is exploits the reduced thermal stability of DNA fragments that contain base mismatches to detect sin

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

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

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

266 1L2 and Trex2 causes massive accumulation of DNA fragments throughout the cornified layers of the ton

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

268 he attachment of modular barcode tags to the DNA fragments to be sequenced facilitated the simultaneo

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

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

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

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

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

274 We found that a 1000-bp DNA fragment upstream of the ATG translation start site

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

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

277 We isolated a 1614-bp DNA fragment upstream of the initiation codon of Epac1 g

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

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

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

281 ridized microparticle bound and free cleaved DNA fragments was observed in real time and label-free f

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

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

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

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

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

287 ing the method based on cyclization of short DNA fragments, which allows very accurate determination

288 ed to assemble plasmids from several ectopic DNA fragments, which are all introduced in yeast cells b

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

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

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

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

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

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

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

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

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

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

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).