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1 lso prepared using the same DNA amplified by multiple displacement amplification.
2  other amplification methodologies including multiple displacement amplification.
3 capsulated into droplets and amplified using multiple displacement amplification.
4            Here, we describe digital droplet multiple displacement amplification, a method that enabl
5 s et al. present a method combining improved multiple displacement amplification and FACS, to obtain
6  using a #10 K file and then amplified using multiple displacement amplification and PCR-amplified wi
7 e-flow-sorted cells, amplifying their DNA by multiple displacement amplification and sequencing all c
8 it-depletion with phi29 DNA polymerase-based multiple displacement amplification and shotgun DNA sequ
9 he polar bodies and oocytes are amplified by multiple displacement amplification and, together with m
10 ing whole-genomic DNA prior to SNP analysis, multiple displacement amplification, and OmniPlex techno
11 e-genome amplification (SWGA), an isothermal multiple-displacement amplification-based method, to eff
12 DNA template in each aliquot is amplified by multiple displacement amplification, converted into barc
13                           When combined with multiple displacement amplification, detection of a sing
14  human donor were subjected to droplet-based multiple displacement amplification (dMDA) to generate l
15                    We applied in-gel digital multiple displacement amplification (dMDA) to purified D
16 n-sensitive restriction enzyme digestion and multiple displacement amplification for selective detect
17                                 Downsides of multiple displacement amplification include coverage bia
18                DNA samples were amplified by multiple displacement amplification (MDA) and a high-fid
19              Comparison of balanced-PCR with multiple displacement amplification (MDA) demonstrates e
20 (IMS) for targeted bacterial enrichment with multiple displacement amplification (MDA) for whole-geno
21 (IMS) for targeted bacterial enrichment with multiple displacement amplification (MDA) for whole-geno
22                                              Multiple displacement amplification (MDA) has become the
23                                              Multiple displacement amplification (MDA) is an isotherm
24  needs to be amplified before sequencing and multiple displacement amplification (MDA) is widely used
25            Whole genome amplification by the multiple displacement amplification (MDA) method allows
26                   New lab techniques such as multiple displacement amplification (MDA) of single cell
27  now be sequenced using DNA amplified by the Multiple Displacement Amplification (MDA) reaction.
28 form was used to generate genomic DNA by the multiple displacement amplification (MDA) technique from
29                                       We use Multiple Displacement Amplification (MDA) to amplify the
30                   Here, we introduce droplet multiple displacement amplification (MDA), a method that
31 escence-activated cell sorting, whole-genome multiple displacement amplification (MDA), and subsequen
32                  Current approaches, such as Multiple Displacement Amplification (MDA), offer high ge
33  first time a recently developed WGA method, multiple displacement amplification (MDA), to amplify si
34                 We describe a method, termed multiple displacement amplification (MDA), which provide
35 combinase polymerase amplification (RPA) and multiple displacement amplification (MDA).
36  the whole-genome amplification technique of multiple displacement amplification (MDA).
37 sted the two most commonly used WGA methods, multiple displacement amplification (MDA-Qiagen REPLI-g
38                                              Multiple-displacement amplification (MDA) has been used
39                                Here, we used multiple-displacement amplification (MDA) of cellular DN
40  flow-sorting of single nuclei, time-limited multiple-displacement amplification (MDA), low-input lib
41     Here we present WGA-X, a method based on multiple displacement amplification of DNA that utilizes
42 MIP-Seq), an experimental approach involving multiple displacement amplification of individual provir
43         These properties allow it to perform multiple displacement amplification of plasmid DNA with
44                              Digital droplet multiple displacement amplification provides a simple an
45                Single-cell genomics (SCG) by multiple displacement amplification provides a technical
46 essed these issues by developing single-cell multiple displacement amplification (SCMDA) and a genera
47           The protocol comprises single-cell multiple displacement amplification (SCMDA), which ensur
48 st time coupled a microfluidic platform with multiple displacement amplification technology to perfor
49                           When combined with multiple displacement amplification, this methodology ca
50  have developed a method based on isothermic multiple-displacement amplification to allow access to a
51 e is exhaustive single-cell sequencing using multiple displacement amplification, which is simply int