ライフサイエンスコーパス: DNA barcode

1 om each individual is identified by a unique DNA barcode.

2 fold when compared to the use of a monomeric DNA barcode.

3 on, with each domain being assigned a unique DNA barcode.

4 l library containing a highly diverse set of DNA barcodes.

5 fication through the use of species-specific DNA barcodes.

6 roach: high-resolution lineage tracking with DNA barcodes.

7 roducts, whilst still preserving the cognate DNA barcodes.

8 ction of ligand binding by quantification of DNA barcodes.

9 image-based readout of short (20-base-pair) DNA barcodes.

10 led through the use of reagents labeled with DNA barcodes.

11 ies diversity and community composition with DNA barcodes.

12 fied 265 specimens to species or genus using DNA barcodes.

13 and contig overlap tailored to the needs of DNA barcoding.

14 ent and can introduce serious ambiguity into DNA barcoding.

15 d in the literature or be identified through DNA barcoding.

16 a cost-effective method for high-throughput DNA barcoding.

17 idual droplets for messenger RNA and genomic DNA barcoding.

18 and its molecular identity was verified with DNA barcoding.

19 methods based on microscopic examination and DNA barcoding.

20 esigned a three-step pipeline for multilocus DNA barcoding.

21 Here, we DNA-barcoded 208 dried and processed fins and in doing s

22 Here, we use DNA barcoding [4] to validate the species identity of 14

23 mitochondrial and nuclear markers, 5670 bp), DNA-barcoding (98 Holarctic specimens), morphometry (88

24 Enrichment Barcoding (MEBarcoding) for plant DNA Barcoding, a cost-effective method for high-throughp

25 d using sequence-based applications, such as DNA barcoding, a diagnostic technique that utilizes PCR

26 PATROL formulates a set of DNA-barcoded, activity-based nanosensors (ABNs) into an

27 DNA barcoding aids in identification and advances specie

28 We confirmed that the use of DNA barcoding allowed unequivocal identification of this

29 Each mutant contains unique DNA barcodes, allowing the collection to be screened as

30 es of nucleic acid barcodes (b-mRNA versus a DNA barcode) altered in vivo delivery, suggesting that t

31 Combining continental-wide genomic and DNA-barcoding analyses, we reconstructed the historical

32 ergent from orthologous mtDNA sequences, and DNA barcoding analysis incorrectly overestimates the num

33 a high-throughput quantitative method using DNA barcodes and a next-generation sequencing technology

34 equencing to generate large amounts of plant DNA barcodes and build more comprehensive barcode databa

35 alytical challenges to lineage tracking with DNA barcodes and discuss its applications to studies of

36 ge subunit (LSU) rRNA gene have been used as DNA barcodes and for phylogenetic studies in different e

37 By using heritable DNA barcodes and high-throughput next-generation single-

38 esign-M can also design primers that include DNA barcodes and minimize primer dimerization.

39 NT-seq quantifies how dozens of LNPs deliver DNA barcodes and mRNA into cells, the subsequent protein

40 t couples multiplex PCR with sample-specific DNA barcodes and next-generation sequencing to enable hi

41 This study used DNA barcoding and 16 S rRNA sequencing as a method to id

42 Based on DNA barcoding and haplotype-inferred evidence for deep g

43 mediated homology-directed repair (HDR) with DNA barcoding and high-throughput sequencing to simultan

44 Emerging technologies like DNA barcoding and mass spectrometry are still in their i

45 High-complexity DNA barcoding and mathematical modeling indicate a high

46 d assessment of faunal biodiversity, akin to DNA barcoding and metabarcoding.

47 ose a potential impediment to application of DNA barcoding and metagenomics for biomonitoring using b

48 DNA barcoding and population genetic studies have reveal

49 n a form that can be analyzed directly using DNA barcoding and pyrosequencing.

50 Therefore, we integrated DNA barcoding and rearing of larvae to identify wood-bor

51 Here we combine microfluidics, DNA barcoding and sequencing to collect chromatin data a

52 imal connectome sequencing), which leverages DNA barcoding and sequencing to map connectivity from si

53 Using DNA barcoding and split-pool decoding, we created a larg

54 cola, and S. integrifolia were identified by DNA barcoding, and phylogenetic relationships were estab

55 Complementary approaches (stomach contents, DNA barcoding, and stable isotopes) were used to examine

56 highly multiplexed signal amplification via DNA-barcoded antibodies and orthogonal DNA concatemers g

57 to enable combinatorially indexed dsc-seq of DNA-barcoded antibodies from over 10(5) cells per reacti

58 The development of DNA-barcoded antibodies to tag cell surface molecules ha

59 SM-Omics uses DNA-barcoded antibodies, immunofluorescence or a combina

60 aining with either fluorophore-conjugated or DNA-barcoded antibodies, through an optimized immunostai

61 velopment and validation of a photocleavable DNA barcode-antibody conjugate method for rapid, quantit

62 B cells are mixed with a panel of DNA-barcoded antigens so that both the antigen barcode(s

63 Here, we used a DNA barcoding approach to generate the genotype-to-fitne

64 Through a DNA barcoding approach, we show that the clinically appr

65 In MP3-seq, DNA barcodes are associated with specific protein pairs

66 DNA barcodes are attached to proteins collectively via r

67 t identifications at the species-level using DNA barcodes are feasible, cost-effective, and reliable,

68 Chromosomally integrated DNA barcodes are then co-amplified with endogenous marke

69 Traditional methods like DNA barcoding are limited, especially for processed food

70 Despite the utility of DNA barcodes as a multiplexing tool, their susceptibilit

71 boratory and our own used retrovirus-encoded DNA barcodes as unambiguous lineage-tracing tools to add

72 This study demonstrates the utility of DNA barcoding as a tool for regulatory agencies.

73 Findings highlight DNA barcoding as an appropriate tool for mold identifica

74 sed on host identification by morphology and DNA barcoding, as well as the morphology and phylogeneti

75 is study was to compare the performance of a DNA-barcode assay with fatty acid profile analysis to au

76 tes single cell transcriptome profiling with DNA barcode based clonal tracking in patient-derived xen

77 0 genera and 12 families were analyzed using DNA barcodes based on the ITS2 and psbA-trnH sequences.

78 Here, we study the effect of numts on DNA barcoding based on phylogenetic and barcoding analys

79 that these data will motivate discussions on DNA barcoding based species identification as applied to

80 ication of nanoparticle delivery (FIND) is a DNA barcode-based system designed to measure how over 10

81 e identified and screened for host DNA using DNA barcoding-based blood meal analysis.

82 matK + trnH-psbA is currently applicable for DNA barcoding-based phylogenetic studies on forest commu

83 chain blocking group to enable synthesis of DNA barcoded beads having capture sequences for the cons

84 om tissue sections onto a surface covered in DNA-barcoded beads with known positions, allowing the lo

85 to sensitively read out compact and diverse DNA barcodes by imaging will facilitate a broad range of

86 a relatively new method based on the use of DNA barcodes can authenticate the biological origin of t

87 DNA barcodes can be used to identify cryptic species of

88 escent proteins are limited in number, while DNA barcodes can only be read after cell lysis.

89 This approach of DNA-barcoding can be broadened to encompass additional r

90 Tracking of DNA barcoded cell lineages revealed that soft ECM consis

91 roliferation assay on a pooled collection of DNA-barcoded cell lines, we identify a subset of cancer

92 alidation of DOS-DEL-1, a library of 107 616 DNA-barcoded chiral 2,3-disubsituted azetidines and pyrr

93 We quantified RSD by two DNA barcode combinations (rbcL + matK and rbcL + matK +

94 sembly onto streptavidin (SA) to generate SA-DNA barcode complexes to increase the number and density

95 The resulting DNA-barcoded compounds exhibit unprecedented ring and to

96 Here, we propose a binding-based screen of DNA-barcoded compounds on a target protein in the presen

97 o-CRISPR" assay, we used anti-CXCL9 antibody-DNA barcode conjugates to target CXCL9 and amplify fluor

98 ve approach involving chemical profiling and DNA barcoding could be applied for authentication of Ice

99 h analysis of over 600 specimens, we provide DNA barcode coverage for 35 described species and 70 mol

100 compared with morphological identifications, DNA barcodes (cytochrome oxidase I) revealed significant

101 n under-representation of parasitoids within DNA-barcode databases (we estimate <5% have a barcode).

102 combination of morphological and multi-locus DNA barcoding diagnoses of diverse arthropod lineages.

103 However, DNA-barcoding discovered established populations of L. n

104 DNA bioconjugation assays in DNA biosensor, DNA barcode, DNA nanostructures, and DNA ultra-resolutio

105 For DNA barcoding, DNA was extracted from the wood of the se

106 we add complete nuclear genome sequencing to DNA barcoding, ecological distribution, natural history,

107 DNA barcodes enable Oxford Nanopore sequencing to sequen

108 Use of biotinylated DNA barcodes enabled self-assembly onto streptavidin (SA

109 Combining microfluidics and DNA barcoding enables simultaneous targeting of tens to

110 compound collections individually linked to DNA barcodes, facilitating pooled construction and scree

111 eninsula with unprecedented resolution (3502 DNA barcodes for all 228 species), creating a reliable s

112 length proteins covalently coupled to unique DNA barcodes for analysis by sequencing can be used for

113 The database should provide DNA barcodes for data retrieval and similarity search.

114 Six DNA regions were evaluated as potential DNA barcodes for Fungi, the second largest kingdom of eu

115 The effectiveness of the DNA barcodes for identification (level of discrimination

116 latform employs novel affinity-discriminated DNA barcodes for multistate decoding with exponential mu

117 Our integrated approach confirmed novel DNA barcodes for seven species (10 specimens) of woodbor

118 Our database of DNA barcodes for Welsh native flowering plants and conif

119 n one sample, illustrating the usefulness of DNA barcoding for evaluating the safety of honey.

120 egion were developed by examining over 8,000 DNA barcodes from species in the U.S. Food and Drug Admi

121 To determine how well DNA barcodes from the chloroplast region perform in fore

122 from each treatment and processed to produce DNA barcodes from the mitochondrial gene cytochrome c ox

123 DNA barcoding greatly enhanced dietary resolution and se

124 We suggest that a DNA barcoding guidelines should be developed involving t

125 lling, and when identified correctly through DNA barcoding, had on average lower mercury than the oth

126 ial of a double nanopore system to determine DNA barcodes has been demonstrated experimentally.

127 Recently, clonal labeling of cells using DNA barcodes has emerged as a powerful approach for iden

128 Species identification using DNA barcodes has revolutionized biodiversity sciences.

129 identification using DNA sequences, known as DNA barcoding has been widely used in many applied field

130 Genomic DNA barcoding has emerged as a sensitive and flexible to

131 divergence among sister species, traditional DNA barcoding has not been successful for differentiatio

132 Molecular methods, such as DNA barcoding, have the potential to enhance biomonitori

133 completed in 1.5 weeks, while automated RNA/DNA barcode hybridization and RNA/DNA imaging typically

134 composition are based on morphology-based or DNA barcode identification of individuals.

135 DNA barcodes identified 42 species and haplotypes across

136 Our results demonstrate that DNA barcodes identifying cells within pooled sequencing

137 658 base pairs of the cytochrome c oxidase I DNA barcode in 1,010 specimens from eleven orders of art

138 Here we examined mitochondrial DNA barcodes in a global urban pest, the American cockro

139 present an approach for engineering evolving DNA barcodes in living cells.

140 Deletion strains containing unique DNA barcodes in place of regulator genes were mixed with

141 me b oxidase (COB), have been used to assess DNA barcoding in dinoflagellates, and both failed to amp

142 nanoparticles (LNPs) using species-agnostic DNA barcoding in tumor-bearing mice.

143 Dual DNA barcodes inserted into each mutant enables verificat

144 how that we can engineer phages by inserting DNA barcodes into newly identified inessential regions,

145 By incorporating sample-specific DNA barcodes into the amplicons, we analyzed 48 samples

146 In Epi-ID, chromatin status on DNA barcodes is interrogated by chromatin immunoprecipit

147 Recoverability of DNA barcodes is lower using herbarium specimens, compare

148 DNA barcoding is a valuable tool to support species iden

149 DNA barcoding is an attractive technology, as it allows

150 In vivo DNA barcoding is used to discover a novel LNP that deliv

151 DNA-barcoding is an alternative to this and the use of H

152 chnologies, sample identification (e.g., via DNA barcoding) is still most often done with Sanger sequ

153 Multiplexing (TaG-EM), involves inserting a DNA barcode just upstream of the polyadenylation site in

154 Using DNA barcode-labeled MHC-I multimers, we find CD8(+) T ce

155 -specific neopeptide libraries consisting of DNA barcode-labelled pMHC multimers in a cohort of 24 pa

156 The assembly of DNA barcode libraries is particularly relevant within sp

157 uences were then compared to a comprehensive DNA barcode library of the Zingiberales.

158 tions and 101 individuals, built a Tribolium DNA barcode library, and designed species-specific prime

159 DNA barcodes linked to genetic features greatly facilita

160 sted 96 samples for each of the four primary DNA barcode loci in plants: rbcL, matK, trnH-psbA, and I

161 Using the plant DNA barcode markers rbcL and matK, we have assembled 97.

162 ple parallel amplification primers, multiple DNA barcode markers, 454-pyrosequencing, and Illumina Mi

163 using an Illumina Miseq platform to sequence DNA barcode markers.

164 ide polymorphisms (SNPs) available with core DNA barcoding markers.

165 The DNA barcodes matK-trnT and atpB-rbcL provided unique pol

166 High-throughput sequencing of environmental DNA barcodes (metabarcoding) offers an alternative to de

167 approach will eclipse existing single-locus DNA barcoding methods as a means to better understand th

168 s to better understand species overlap using DNA barcoding methods suggest coral species are widely d

169 Here we pair rapid DNA barcoding methods with swift assessment of morpholog

170 Here we perform nanopore sequencing of DNA-barcoded molecular probes engineered to recognize a

171 vative step was to copy both strands of each DNA-barcoded molecule with a primer that allows the subs

172 re we used two high-throughput approaches, a DNA-barcoded mononucleosome library and a humanized yeas

173 h-throughput approach, based on the use of a DNA-barcoded mononucleosome library, to profile the bioc

174 terogeneity and dynamics, we used lentiviral DNA barcoding, mtDNA variants and single cell gene expre

175 Nanopore-based sensing of DNA-barcoded nanostructures may help to improve the desi

176 is based on the streamlined semisynthesis of DNA-barcoded nucleosome libraries with distinct combinat

177 y relationship studies, including the use of DNA-barcoded nucleosome libraries, shows that steric hin

178 ly parallel de novo assembly of high quality DNA barcodes of >1400 bp.

179 We used DNA barcoding of a ~ 830 bp fragment from the SSU rDNA t

180 DNA barcoding of anopheline larvae sampled in the 2019 w

181 However, DNA barcoding of cellular proteins remains challenging,

182 Here, we used inducible clonal DNA barcoding of endogenous adult HSCs to trace their co

183 Here, we use DNA barcoding of fecal samples to compare the diet of mo

184 By using DNA barcoding of nuclear ribosomal internal transcribed

185 DNA barcoding of tropical insects reared by a massive in

186 DNA barcoding offers an efficient way to determine speci

187 atially targeted, rapid photocrosslinking of DNA barcodes onto complementary DNAs in situ with a one-

188 The unique 20 bp DNA 'barcodes' or 'tags' in each deletion strain enable

189 roduce and accumulate diverse mutations in a DNA barcode over multiple rounds of cell division.

190 d the potential for causing a false-positive DNA barcoding paradox have been underestimated.

191 he DNA oligonucleotide library, synthesis of DNA-barcoded peptide constructs, binding of constructs t

192 o main sections: (i) design and synthesis of DNA-barcoded peptide libraries and (ii) use of libraries

193 assays against customizable targets by using DNA-barcoded peptides.

194 .5% success rate achieved by the full-length DNA barcode primers.

195 restriction digestion and amplification with DNA barcoding primers.

196 ces proximity records of any nearby pairs of DNA-barcoded probes, at physiological temperature, witho

197 ntified as Saccharomyces bayanus by standard DNA barcoding procedures.

198 DNA barcoding promises to be a useful tool to identify p

199 By screening 11,076 DNA-barcoded proteins expressed from a sequence-verified

200 of diet identifications using a three-locus DNA barcode (rbcL, trnH-psbA and ITS2).

201 the global BOLD Systems database holds core DNA barcodes (rbcL + matK) for about 15% of land plant s

202 orm for densely multiplexed, CRISPR-mediated DNA barcode readout that can potentially evaluate comple

203 Therefore, integrated DNA barcodes, Real-Time PCR assays using TaqMan probes a

204 etto dietary supplements was designed from a DNA barcode reference library created for this purpose.

205 The DNA barcode reference library was developed in BOLD data

206 ragments of the cytochrome c oxidase I (CO1) DNA barcode region were developed by examining over 8,00

207 then used to determine the sequence of the "DNA barcoding" region of the cytochrome c oxidase subuni

208 omic assemblages by deep sequencing of short DNA barcode regions (metabarcoding) have revolutionized

209 Two DNA barcode regions, namely cytochrome c oxidase subunit

210 Using plant DNA barcoding regions (trnL and rpoC) coupled with High

211 We present the first national DNA barcode resource that covers the native flowering pl

212 To date, no studies have effectively applied DNA barcodes sensu strictu in this manner.

213 We replaced each effector with a specific DNA barcode sequence by allelic exchange and co-infected

214 ate how highly resolved phylogenies based on DNA barcode sequence data will enhance research focused

215 These DNA barcode sequences are also used to reconstruct a rob

216 ur approach recovers a greater proportion of DNA barcode sequences from individuals than does convent

217 ved molecular phylogenies derived from these DNA barcode sequences have the potential to improve inve

218 m global CTFS-ForestGEO network, we analyzed DNA barcoding sequences of 1277 plant species from a wid

219 The tracking of lineage frequencies via DNA barcode sequencing enables the quantification of mic

220 e in many individuals, we used combinatorial DNA barcode sequencing to measure the fitness effects of

221 nuclear proteome, is followed by multiplexed DNA-barcode sequencing.

222 e analysed the RV transcriptome by combining DNA-barcoded smFISH of rotavirus-infected cells.

223 veness of hundreds of molecularly annotated 'DNA-barcoded' solid tumor cell lines in multiplexed form

224 Here, we establish DNA barcoding, species-specific PCR, and real-time PCR t

225 Whereas DNA barcoding strives for rapid and inexpensive generati

226 roup of about 2000 described extant species, DNA barcoding studies have revealed large amounts of unr

227 eed for comprehensive reference databases in DNA barcoding studies, especially when dealing with inva

228 tern Cape and Gauteng) were identified using DNA barcoding, supplemented in certain cases with mitoch

229 To enhance detection sensitivity, the DNA barcode system was engineered by introducing multipl

230 In this approach, we generate DNA barcode-tagged AAV libraries and determine a spectru

231 to permit, within many droplets in parallel, DNA barcode tagging together with the mRNA molecules fro

232 ed intermolecular network of proximal unique DNA barcodes tagging complementary DNA molecules inside

233 Single-cell sequencing experiments use short DNA barcode 'tags' to identify reads that originate from

234 cation (MDA), low-input library preparation, DNA barcoding, targeted capture and next-generation sequ

235 but uncovered 14-fold (41%) higher rate via DNA barcoding targeting the chloroplast rbcL gene.

236 The DNA barcode technique was applied to identify plant food

237 hem to second-generation sequencing, using a DNA barcoding technique that allowed us to quantify inde

238 otland were assessed using real-time PCR and DNA barcoding techniques.

239 ses of clonal dynamics in SCP mixtures using DNA barcode technology revealed selection for distinct c

240 also rely on genetic analyses including the DNA barcoding technology.

241 We design an orthogonal panel of DNA-barcoded tetramers to simultaneously detect multiple

242 We constructed error-correcting DNA barcodes that allow one run of a massively parallel

243 This study was undertaken to generate DNA barcodes that could be utilized in monitoring and cu

244 modular bacterial tags (MoBacTags) encoding DNA barcodes that enable tracking of near-isogenic bacte

245 ethods have been developed that add a unique DNA barcode to individual samples prior to pooling and s

246 mor growth dynamics and tagged with a unique DNA barcode to track their fate in multiclonal mixtures

247 Following target binding, this method allows DNA barcodes to be photoreleased in solution, enabling e

248 Here, we used expressed DNA barcodes to clonally trace transcriptomes over time

249 cing (scLT) methods use expressed, heritable DNA barcodes to combine cell lineage readout with single

250 op peptide-MHC (pMHC) tetramers labeled with DNA barcodes to detect single T cells by droplet digital

251 ule bisulfite sequencing and sample-specific DNA barcodes to determine the spectrum of MLH1 promoter

252 encoded in the number and sequence of short DNA barcodes to generate preparatory amounts of nanopart

253 uencing (Dub-seq), a method that uses random DNA barcodes to greatly increase experimental throughput

254 NA and recent single-cell RNAseq methods use DNA barcodes to identify samples and cells, and the barc

255 with the Genera of Fungi project, which adds DNA barcodes to known biodiversity and corrects the appl

256 plex (MHC) multimers labeled with individual DNA barcodes to screen >1,000 peptide specificities in a

257 l microfluidic channels were used to deliver DNA barcodes to the surface of a tissue slide, and cross

258 Both chemotypes were confirmed with DNA barcoding to be M. speciosa.

259 In this study, we used DNA barcoding to compare the diversity and composition o

260 e results demonstrate (i) the sensitivity of DNA barcoding to detect plant feeding in malaria vectors

261 applicability of morphometric parameters and DNA barcoding to detect the adulterated timber sources.

262 We used DNA barcoding to determine the taxonomic identity of 449

263 PLC-QToF-MS chemical profiling together with DNA barcoding to distinguish species and chemotypes of t

264 sse CRISPR ribonucleoprotein injections, and DNA barcoding to enable large-scale functional genetic s

265 use of solid-state nanopores and multiplexed DNA barcoding to identify and characterize oligomers fro

266 This prompted us to use plant DNA barcoding to identify plants that field-caught mosqu

267 ose of this study was to test the ability of DNA barcoding to identify the plant origins of processed

268 Here, we use DNA barcoding to identify, from just a few recovered too

269 ged frozen fishery products, this study used DNA barcoding to investigate the breaded hake and plaice

270 limitations with a technology that leverages DNA barcoding to profile chromatin quantitatively and in

271 acterizing Pi-Lipids, we use high-throughput DNA barcoding to quantify how 65 chemically distinct LNP

272 Using DNA barcoding to test 109 chemically distinct LNPs in vi

273 s issue, we have demonstrated the utility of DNA barcoding to verify the taxonomic identity of fungi

274 or visualizing DNA sequence and using these 'DNA barcodes' to search complex mixtures of genomic mate

275 ghly examines the latest prospective lineage DNA barcode tracing technologies.

276 h traditional taxonomy and known, individual DNA barcodes ("traditional samples") or processed with m

277 a, Zea mays and Capsicum annuum) using plant DNA barcodes trnL and psbA-trnH.

278 t hundreds of genomic locations by combining DNA barcoding, unique split-pool encoding, and single ce

279 ll types in a single culture with the aid of DNA barcodes: unique sequences of DNA introduced to the

280 ersisting cells and identified by sequencing DNA barcodes uniquely labeling each of the tested cytoki

281 by converting a transcriptional event into a DNA barcode using a retron reverse transcriptase and the

282 e collected species was performed throughout DNA barcoding using ITS, rbcL, rpoC1 and matK sequences.

283 DNA barcoding utilizes species-specific DNA sequence inf

284 ralizing antibodies to block binding between DNA-barcoded viral spike protein subunit 1 and the human

285 ano-oscillator platform using self-assembled DNA-barcoded virion sensors is developed to address the

286 Multiamplicon next-generation DNA barcoding was able to recover sequences correspondin

287 Therefore, DNA barcoding was used to investigate sales of shark pro

288 d to AAV capsid mutant libraries tagged with DNA barcodes, we can draw a high-resolution map of AAV c

289 Using CRISPR/Cas9 technology and specific DNA barcodes, we devised a strategy to recapitulate and

290 DNA barcodes were used to identify LNP(HNSCC), a novel L

291 is report, we demonstrate that a three-locus DNA barcode when applied to 296 species of woody trees,

292 tive and practical alternative to exhaustive DNA barcoding when preparing sequencing libraries for hu

293 oximity ligation of RNAs with protein-linked DNA barcodes, which are subsequently decoded through seq

294 e complex organic compounds with amplifiable DNA barcodes, which could be easily incorporated into a

295 cation of detection probes, as antibodies or DNA barcodes, which is complex and time-consuming.

296 however, this is especially problematic for DNA barcoding, which attempts to characterize all living

297 onfirmed morphologically and molecularly via DNA barcoding with published primers.

298 and apply FateMap, a framework that combines DNA barcoding with single-cell RNA sequencing, to reveal

299 rmed a genome-wide screen using a library of DNA-barcoded yeast deletion mutants grown in copper-supp

300 aries displayed on phage that carries silent DNA-barcodes yields macrocyclic libraries in which the a