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1 sine methylation was measured in blood using pyrosequencing.
2  (96/126) with follow-up target-specific PCR/pyrosequencing.
3 first examination were analyzed by ultradeep pyrosequencing.
4        All controls screened negative by PCR/pyrosequencing.
5  analyzed by 16S ribosomal RNA gene amplicon pyrosequencing.
6 re collected and profiled with 16S rRNA gene pyrosequencing.
7 fic DNA methylation analysis in plants using pyrosequencing.
8 ent in sorted cells from spleen and blood by pyrosequencing.
9 olution using high-throughput locus-specific pyrosequencing.
10 ection or a limitation of the sensitivity of pyrosequencing.
11      Findings were validated using bisulfite pyrosequencing.
12       The microbiota was monitored using 454 pyrosequencing.
13 e expression, and top CpGs were validated by pyrosequencing.
14      The methylation status was confirmed by pyrosequencing.
15 ks and 6 months by 16S-based GS-FLX-titanium-pyrosequencing.
16 as performed on cellular RNA using Roche/454 pyrosequencing.
17 ory protocol) and by bacterial 16S rRNA gene pyrosequencing.
18 ma RNA and cell DNA specimens by OLA and 454 pyrosequencing.
19 ic, with validation of findings by bisulfite pyrosequencing.
20 A, and one at 69% by OLA and not detected by pyrosequencing.
21 es in the leptin promoter was measured using pyrosequencing.
22 ed annually between 5 and 14 years of age by pyrosequencing.
23 (n = 73) and at age of 4.5 years (n = 61) by pyrosequencing.
24  Clostridiaceae) inferred from 16S rRNA gene pyrosequencing.
25 nd 24 months were characterized by 16S-based pyrosequencing.
26 ta, across this landscape using qPCR and 454 pyrosequencing.
27 ota composition (dysbiosis) was evaluated by Pyrosequencing.
28 o those that were previously described using pyrosequencing.
29 ate landscape using 16S rRNA gene tagged 454 pyrosequencing.
30 A quantitative polymerase chain reaction and pyrosequencing.
31 pG sites within the SFRP1 promoter region by pyrosequencing.
32 mpared with standard single-region Roche 454 Pyrosequencing.
33 g enzymes and transporters were evaluated by pyrosequencing.
34 mor tissues and 9 matching normal tissues by pyrosequencing.
35 eir promoter regions was analyzed by PCR and pyrosequencing.
36 idization (FISH), and 16S rRNA gene amplicon pyrosequencing.
37 rom human liver (n = 22) was performed using pyrosequencing.
38  was compared to quantitative PCR (qPCR) and pyrosequencing.
39 rongosa National Park, Mozambique) using 454 pyrosequencing.
40  tissues of the offspring were determined by pyrosequencing.
41 d and analyzed by 16S ribosomal RNA targeted pyrosequencing.
42        Microbial taxa were identified by 16S pyrosequencing.
43 y and environmentally relevant species using pyrosequencing.
44 arate validation cohort of 30 MF patients by pyrosequencing.
45 s DHAs on DNA methylation reversal using DNA pyrosequencing.
46 C4 in response to exposure were validated by pyrosequencing.
47 vered Antarctic lakes by 16S rRNA gene-based pyrosequencing.
48 ity was tracked using 16S rRNA gene amplicon pyrosequencing.
49 munity data from two distinct studies by 454 pyrosequencing.
50 a viridis and Actinia equina using 16 S rDNA pyrosequencing.
51 n additional tumor samples using RT-qPCR and pyrosequencing.
52 r working with the raw flowgrams obtained by pyrosequencing.
53  16S rRNA gene polymerase chain reaction and pyrosequencing.
54  Candidate genes were validated by bisulfite pyrosequencing (30 AGA, 21 SGA) and also analyzed in cor
55                                  For 42 real pyrosequencing ('454') datasets, assembly increased the
56 ); among 60 (61%) A (H3N2) viruses tested by pyrosequencing, 53 (88%) belonged to the drifted 3C.2a g
57 ssay results with phenotypic DST (97.0%) and pyrosequencing (97.8%) results from the same clinical sa
58                                       Third, pyrosequencing allowed the detection of OTUs that were e
59                            Our 16S rRNA gene pyrosequencing analyses revealed that the soil type dete
60                                     Based on pyrosequencing analyses, beta-Proteobacteria dominated i
61                                              Pyrosequencing analysis and qPCR revealed a dramatic tra
62  AMF diversity was determined using 18S rDNA pyrosequencing analysis of 360 soil samples taken at six
63                                              Pyrosequencing analysis of CpG rich regions, and CpG din
64                         16S rDNA metagenomic pyrosequencing analysis of the microbial communities ass
65                                              Pyrosequencing analysis revealed that Geobacter species
66                        Methylation-sensitive pyrosequencing analysis showed that CpG sites at the Thy
67                                              Pyrosequencing analysis was conducted to determine the s
68                    Using highly quantitative pyrosequencing analysis, we found extensive and highly v
69 dividuals for miRNA expression profiling and pyrosequencing analysis.
70 mucosal microbiota assessed by 16S rRNA gene pyrosequencing and (1)H NMR spectroscopy.
71                           The application of pyrosequencing and allele-specific PCR techniques establ
72 etagenomic shotgun sequencing, 16S rRNA gene pyrosequencing and cloning/sequencing hgcAB gene product
73 ched genome-wide significance, replicated by pyrosequencing and correlated with expression difference
74 ormed on stool samples via 16S ribosomal RNA pyrosequencing and correlations between disease severity
75                      Concordance between PCR/pyrosequencing and culture was 96.9% (1,085/1,120) for U
76  (n = 15) were analyzed by 16S ribosomal RNA pyrosequencing and culture-based methods.
77                                   Bisulphite pyrosequencing and demethylation treatment showed that N
78 umole photons s(-1) m(-2) ) and combined 454-pyrosequencing and enzymatic activity assays to evaluate
79 ological settings by 16S rRNA gene-based 454 pyrosequencing and explored their relationships to filtr
80                                              Pyrosequencing and fluorescence in situ hybridization an
81 particle purification, genome amplification, pyrosequencing and gene/genome reconstruction and annota
82 me were investigated using 16S rRNA amplicon pyrosequencing and high-throughput quantitative PCR.
83              16S ribosomal RNA gene amplicon pyrosequencing and HPV DNA testing were conducted annual
84                            Here, we used 454 pyrosequencing and identity/divergence grid sampling to
85 firmed sepsis samples with Universal 16S PCR/pyrosequencing and in 76.4% (96/126) with follow-up targ
86 ycobacterium tuberculosis isolates combining pyrosequencing and IS6110 polymorphism.
87                  Here, we used 16S rRNA gene pyrosequencing and metagenomic sequencing to examine ora
88                            Quantification by Pyrosequencing and MLPA demonstrated levels of mutant ce
89 trations of approximately 2%, one at 8.8% by pyrosequencing and not detected by OLA, and one at 69% b
90 levels of resistant variants not detected by pyrosequencing and possibly below the threshold for phen
91                                              Pyrosequencing and qPCR revealed that laundry water micr
92 hberg) and verified hits using bisulfite PCR pyrosequencing and qPCR.
93 ces samples were analyzed by high-throughput pyrosequencing and quantitative real-time polymerase cha
94 thylation and mRNA levels by using bisulfite pyrosequencing and quantitative RT-PCR in monocytes in v
95 sing over 7 million cDNA sequences from both pyrosequencing and Sanger sequencing, we found that a mu
96                        According to 16S rRNA pyrosequencing and shotgun metagenome sequencing analyse
97                               We applied 454-pyrosequencing and single-cell RT-PCR of bulk and sorted
98 ymorphisms were typed using a combination of pyrosequencing and TaqMan genotyping assays.
99 mmunity DNA from MW309 was analyzed with 454 pyrosequencing and terminal restriction fragment length
100  flocks was performed using Illumina and 454 pyrosequencing and the sequenced genomes compared to the
101 e PCR), DNA methylation status (by bisulfite pyrosequencing), and GAL peptide by RIA of the GAL syste
102  DMP was successfully validated by bisulfite-pyrosequencing, and identified DMPs were tested in postm
103 n primers, multiple DNA barcode markers, 454-pyrosequencing, and Illumina MiSeq sequencing to the sam
104 r 16S rRNA gene techniques (clone libraries, pyrosequencing, and real-time PCR), we show that polymet
105 pecific polymerase chain reaction, bisulfite pyrosequencing, and restriction enzyme-polymerase chain
106 tractive hybridisation (SSH) followed by 454 pyrosequencing, and RT-qPCR methods.
107 uantitative polymerase chain reaction (PCR), pyrosequencing, and standard culture techniques.
108 ogical studies, we developed and validated a pyrosequencing approach that enables identification of s
109 cts were sequenced using both Sanger and 454 pyrosequencing approaches.
110 ns identified by Universal 16S rRNA gene PCR/pyrosequencing as containing staphylococci, streptococci
111 e promoter of ADCYAP1R1 (cg11218385) using a pyrosequencing assay in DNA from white blood cells.
112                                            A pyrosequencing assay was established that reproduced the
113                                      A novel pyrosequencing assay was used to determine genetic group
114 ured by bisulphite-polymerase chain reaction pyrosequencing assay.
115 ions were verified by MassARRAY Epityper and pyrosequencing assays and could be further replicated in
116 R amplification on bisulfite-treated DNA and pyrosequencing assays as well as the quantification of t
117 A methylation using bisulfite conversion and pyrosequencing assays on DNA from buccal cells provided
118 distinguish these variants reliably and thus pyrosequencing assays were developed.
119 ee sources are suitable for standard PCR and pyrosequencing assays.
120  cortex and performed quantitative bisulfite pyrosequencing at nine loci.
121  The virus populations were sequenced by 454 pyrosequencing at the end of passaging, and the results
122 as largely due to bacteria being detected by pyrosequencing but not by culture.
123 s readily adopted by another laboratory with pyrosequencing capabilities.
124 riteria for pyrosequence processing or among pyrosequencing, cloning and microscopy, while taxon iden
125 ely 7.5 h when including target-specific PCR/pyrosequencing compared to 27.9 +/- 13.6 h for Gram stai
126 veloped in-house), were utilized to expedite pyrosequencing data analysis.
127          We apply the method to 454 amplicon pyrosequencing data obtained from a malaria virulence ge
128                                              Pyrosequencing data revealed majority overlap in differe
129                                              Pyrosequencing data revealed that the dominant phyla rel
130                        Analysis of ultradeep pyrosequencing data sets derived from virus amplicons fr
131                                          The pyrosequencing data were cross-checked by using the sing
132                                 In addition, pyrosequencing demonstrated higher levels of methylation
133                           Targeted bisulfite pyrosequencing demonstrated that miR-34A was inactivated
134                                Evaluation of pyrosequencing-derived 16S rRNA gene sequences recovered
135                            The 16S rRNA gene pyrosequencing did not have sufficient resolution to ide
136                                              Pyrosequencing errors, consisting mainly of nucleotide i
137 f 16S rRNA-encoding gene sequence reads (454-pyrosequencing) examined viable and total biofilm commun
138                                              Pyrosequencing experiments validated the cell type-speci
139 e assessed HVR1 evolution by using ultradeep pyrosequencing for a cohort of treatment-naive, chronica
140 polymerase chain reaction amplification with pyrosequencing for a rapid approach to generate the comp
141 length p17 and p24 gag were generated by 454 pyrosequencing for all pairs near the time of transmissi
142     We employed bacterial fingerprinting and pyrosequencing for microbiome analysis.
143        Our findings confirm the potential of pyrosequencing for quantifying microbial diversity, but
144 umbricus rubellus through utilizing 16S rRNA pyrosequencing for the first time to establish the micro
145        Independent verification by bisulfite pyrosequencing generally confirmed the percentage methyl
146                                              Pyrosequencing generated more than 150,000 sequences, re
147                                              Pyrosequencing genotyping and sequencing of the voltage
148 anscriptome profiling and gene-specific cDNA-pyrosequencing have documented that transcriptome shock
149 all and medium CMNs using Sanger sequencing, pyrosequencing, high-resolution melting analysis, and mu
150                                              Pyrosequencing identified abundant atypical bacteria in
151                                          DNA pyrosequencing identified hypermethylated regions of the
152                                        Thus, pyrosequencing illustrated that while DB, PRB, and SRB r
153 est were verified by means of locus-specific pyrosequencing in 35 sibling pairs and replicated in an
154 thylation was measured by means of bisulfite pyrosequencing in patients.
155 terval [CI]) for Universal 16S rRNA gene PCR/pyrosequencing included sensitivity of 77.8% (69.5 to 84
156                                              Pyrosequencing indicated biofilm communities were all si
157 lly available high-throughput locus-specific pyrosequencing instruments allow for the simultaneous an
158  motives, which cannot be evaluated by these pyrosequencing instruments due to software limitations.
159 uency by single-genome amplification and 454 pyrosequencing, (iv) virion-associated Env content, and
160                          In summary, shotgun pyrosequencing metagenomic analyses of agricultural dust
161          In this study, we performed shotgun pyrosequencing metagenomic analyses of DNA from dusts fr
162  alignment showed that 19% or 62% of shotgun pyrosequencing metagenomic DNA sequence reads from swine
163          Mutational status was determined by pyrosequencing method, allelic discrimination, or Sanger
164                                      Using a pyrosequencing method, we determined that the tumor posi
165                                              Pyrosequencing methylation and HPV genotyping assays wer
166                                     Baseline pyrosequencing methylation and human papillomavirus (HPV
167 the Sanger sequencing, the 'next generation' pyrosequencing, microarrays, quantitative PCR, and the r
168                          Culture-independent pyrosequencing microbiome analysis was used to examine t
169      However, out of 23 candidates tested by pyrosequencing, none could be confirmed.
170                                       Repeat pyrosequencing of 13 specimens showed reproducible detec
171                                              Pyrosequencing of 16S rDNA is widely used to study micro
172                                              Pyrosequencing of 16S rDNA was used to study changes in
173         Analyses of community composition by pyrosequencing of 16S rRNA and hoxH genes indicate that
174  Fecal and ileal microbiota were analyzed by pyrosequencing of 16S rRNA genes and enumeration of sele
175     In total, 24 samples were examined using pyrosequencing of 16S rRNA genes and various chemical pr
176                                              Pyrosequencing of 16S rRNA genes results revealed an age
177                  Quantitative PCR (qPCR) and pyrosequencing of 16S rRNA genes was used to quantify th
178 ng six marine lakes and one ocean site using pyrosequencing of 16S rRNA genes.
179                                              Pyrosequencing of 16S rRNA transcripts from the indigeno
180                                 By combining pyrosequencing of 18S ribosomal RNA genes with data on m
181 acterization was performed by using 16S rDNA pyrosequencing of 872 nasal swabs collected biweekly fro
182             We demonstrate via 16S rRNA gene pyrosequencing of 922 specimens from 58 subjects that th
183                                  We used 454 pyrosequencing of a normalized adult cDNA library and de
184                        In contrast, SSCP and pyrosequencing of an unrelated single SNP (rs1835740:C >
185  bacterial communities were characterized by pyrosequencing of barcoded 16S rRNA genes and clustered
186              DNA methylation was assessed by pyrosequencing of bisulfite converted DNA and methylated
187 independent sample set of 558 subjects using pyrosequencing of bisulfite-converted DNA (min P-value <
188 ent case-control participants using targeted pyrosequencing of bisulfite-converted DNA.
189            Utilizing extensive transcriptome pyrosequencing of diverse taxa, we established a resolve
190          Direct Sanger sequencing as well as pyrosequencing of environmental isolates demonstrated th
191          Data to support this includes V1-V3 pyrosequencing of formation water and drilling mud, as w
192  and analyzed community composition based on pyrosequencing of fungal internal transcribed spacer (IT
193                                              Pyrosequencing of genetic marker, COI (cytochrome c oxid
194 geting clades of the xoxF gene, and used 454 pyrosequencing of PCR amplicons obtained from the DNA of
195                                 DGGE and 454-pyrosequencing of PCR-amplified 16S rRNA genes were used
196                                              Pyrosequencing of pig caecal 16S rRNA gene amplicons ide
197 MeTIL markers can be determined by bisulfite pyrosequencing of small amounts of DNA from formalin-fix
198 idiopathic IBD (n = 10) were analyzed by 454-pyrosequencing of the 16S rRNA gene and qPCR assays.
199 f 86 school age children was analyzed by 454 pyrosequencing of the 16S rRNA gene fragments.
200 200 paired sputum samples from 93 CF adults; pyrosequencing of the 16S rRNA gene was applied to 59 pa
201                                    Using 454 pyrosequencing of the 16S rRNA gene, we compared bacteri
202  8) and peri-implantitis (n = 6) sites using pyrosequencing of the 16S rRNA gene.
203 ed soil, rhizosphere, and plant roots by 454-pyrosequencing of the 16S rRNA gene.
204 rm and nonfarm children were analyzed by 454-pyrosequencing of the bacterial 16S ribosomal RNA gene.
205                                In this work, pyrosequencing of the bacterial 16S rRNA gene was firstl
206 CM fungal communities were identified by 454 pyrosequencing of the fungal internal transcribed spacer
207      DNA methylation levels were assessed by pyrosequencing of the LINE-1 retroelement promoter in DN
208                                              Pyrosequencing of the PCR amplicons identified a total o
209                                              Pyrosequencing of the pfcrt gene codon 76 region was per
210                                              Pyrosequencing of the two feeding groups found that meth
211        Biofilm samples were analyzed by FLX+ pyrosequencing of the V1 to V4 hypervariable regions of
212 ace sediments were used as templates for tag pyrosequencing of the V4 region of the 18S ribosomal DNA
213  amplicons were subjected to high-throughput pyrosequencing on a Roche 454 GS-FLX platform.
214 centage methylation (%5mC) was analysed with pyrosequencing on buccal DNA.
215 tive was to perform whole-genome shotgun 454 pyrosequencing on the same fecal specimens collected in
216  and homozygote mutant genotypes compared to pyrosequencing or Sanger sequencing.
217                   In conclusion, the OLA and pyrosequencing performed similarly in the quantification
218 c Gram-negative rods had target-specific PCR/pyrosequencing performed.
219                                              Pyrosequencing permits accurate quantification of DNA me
220 e for the presence of similar sequences, the pyrosequencing platform correctly classified all 12 inci
221 le-measure incidence assay by implementing a pyrosequencing platform.
222 sity surveys which used PCR or multiplex 454 pyrosequencing platforms showed that the bacterial diver
223  critical for ligation of the OLA probes and pyrosequencing primers, respectively.
224 hic locations and then conducted 454 shotgun pyrosequencing procedures to obtain 16-24 x coverage of
225                        We analyzed, based on pyrosequencing profiling of the biofilm communities in 1
226 e sample processing was included for PCR and pyrosequencing protocols, the molecular approach yielded
227                               We developed a pyrosequencing (PSQ) assay including eight subassays for
228 rnia Department of Public Health began using pyrosequencing (PSQ) to detect mutations associated with
229 We described AM fungal communities using 454-pyrosequencing, quantified the proportion of root length
230 own of residence, and experimental plate for pyrosequencing reactions.
231 ified by adenosine triphosphate analysis and pyrosequencing, respectively.
232                                          The pyrosequencing results corroborated our analysis, withou
233                                              Pyrosequencing results suggested Dechloromonas and Tetra
234                                 Based on the pyrosequencing results, it appears that clindamycin has
235 actors most likely to affect the accuracy of pyrosequencing results.
236                        The 16S rDNA-targeted pyrosequencing revealed a significant change in the comp
237                                              Pyrosequencing revealed an increase in percentage of Gra
238                                              Pyrosequencing revealed pronounced diversity co-exists w
239                                              Pyrosequencing revealed relatively stable bacterial comm
240                                              Pyrosequencing revealed shared HIV-1 antibody clonal lin
241                                     However, pyrosequencing revealed that 15/15 (100%) of patients ha
242                       16S rRNA gene amplicon pyrosequencing revealed that bacterial communities highl
243   Methylated DNA immunoprecipitation-PCR and pyrosequencing revealed that developmental BPA exposure
244                                              Pyrosequencing revealed that the population belonging to
245            Community analysis using 16S rRNA pyrosequencing revealed the dominance of Methanosarcina
246               16S amplicon analysis (454 FLX pyrosequencing) revealed significantly lower alpha diver
247  49 subjects with paired specimens tested by pyrosequencing, S. aureus was identified from 11 (22%) a
248 2.0%, and at 125 codons (28%; P < 0.0001) by pyrosequencing sensitive to 0.1%.
249                                          454 pyrosequencing showed a significant selection for diazot
250                            16S rRNA amplicon pyrosequencing showed an increase in the relative abunda
251 expression; promoter methylation analysis by pyrosequencing showed no differences in Bmpr1a, Ptch1, S
252                                16S rRNA gene pyrosequencing showed that Gram-positive bacteria affili
253                                              Pyrosequencing showed that novel strains Peptoniphilacea
254 somal RNA gene libraries sequenced using 454-pyrosequencing targeting the V1 to V3 and V7 to V9 regio
255                                     Amplicon pyrosequencing targets a known genetic region and thus i
256 g 15 GIST and 17 PPGL) was performed using a pyrosequencing technique and correlated with SDHC gene e
257                                              Pyrosequencing technology provides an important new appr
258 om DNA analyses of the in situ samples using pyrosequencing technology, we found the highest abundanc
259 gender-matched controls using the bisulphite pyrosequencing technology.
260 ial changes were monitored by amplifying and pyrosequencing the 16 S ribosomal small subunit region.
261 e fecal microbiota from these two species by pyrosequencing the 16S V1-V3 hypervariable regions using
262          We profiled the fecal microbiota by pyrosequencing the gene encoding 16S ribosomal RNA (rRNA
263      We used 16S rRNA gene amplification and pyrosequencing to characterize, for the first time to ou
264                  We used next generation 454 pyrosequencing to discern the whole-body microbiome of t
265 s were subjected to whole-genome shotgun 454 pyrosequencing to identify both fecal bacterial populati
266 ions by using phylogenic microarrays and 454 pyrosequencing to identify microorganisms and functional
267                                      We used pyrosequencing to investigate allelic imbalance of Oxtr
268 tersubtype Env recombinants and utilized 454 pyrosequencing to investigate the distribution of over 4
269 eotrichia (class Spirotrichea), by comparing pyrosequencing to Sanger-sequenced clone libraries and m
270          Here we compared the results of PCR/pyrosequencing to those of culture for detecting bacteri
271  ten-eleven translocation-assisted bisulfite pyrosequencing, to quantify FMR1 5mC and 5hmC levels.
272 es, multicolor flow cytometry, and bisulfite pyrosequencing, to study the effects of H pylori on alle
273                              The initial PCR/pyrosequencing took approximately 5.5 h to complete or a
274 ing microscopy, and molecular biology (i.e., pyrosequencing) tools.
275             In this study, we used ultradeep pyrosequencing (UDPS) to map the viral heterogeneity of
276 uencing (NGS), capillary electrophoresis and pyrosequencing under the term 'NGS+' for typing Y-STRs a
277 ive to 2.0%, at 71 codons (16%; P = 0.78) by pyrosequencing using a cutoff value of >/= 2.0%, and at
278 arine sediment cores by quantitative PCR and pyrosequencing using newly designed DEH 16S rRNA gene ta
279                              Next-generation pyrosequencing validated the congruence of the potential
280                                          454-pyrosequencing was able to recover 10 more families of a
281                                              Pyrosequencing was employed to characterize bacteria and
282 ent for detection of bacteria by culture and pyrosequencing was good for aerobic bacteria such as P.
283                                        While pyrosequencing was more sensitive, detection of mutants
284                           Targeted bisulfite pyrosequencing was performed on a validation cohort of 3
285 ity structure appeared to remain stable when pyrosequencing was performed on samples that were not su
286                                              Pyrosequencing was used for DNA methylation quantificati
287                                          454 pyrosequencing was used to assign operational taxonomic
288 s prior to DNA extraction, and 16S rRNA gene pyrosequencing was used to characterize their bacterial
289                                    Bisulfite pyrosequencing was used to compare the methylation level
290                                              Pyrosequencing was used to confirm the imprinting status
291                                              Pyrosequencing was used to evaluate deviation from monoa
292                           In this study, 454 pyrosequencing was used to identify the bacteria associa
293   Culture-independent high-density Roche 454 pyrosequencing was used to survey the distal gut microbi
294              Next-generation sequencing (454 pyrosequencing) was performed to reveal the CPB transcri
295                                        Using pyrosequencing we followed up the two most differentiall
296                                        Using pyrosequencing, we elucidated how important phylotypes o
297                           DNA extraction and pyrosequencing were done on several core sections in ord
298 tive polymerase chain reaction (PCR) and 454 pyrosequencing were used to analyze bacterial 16S riboso
299 ferent spot positions, quantitative PCR, and pyrosequencing, were used to confirm the role of the can
300 during monochloramine disinfection using PMA-pyrosequencing, while the community structure appeared t

 
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