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1  offspring distribution of highly attractive mated pairs.
2 r correlations among partners' phenotypes in mated pairs.
3  always affected a significant proportion of mated pairs.
4 voyeurs had visual access to a mating or non-mating pair.
5 hen the gene is deleted from both cells of a mating pair.
6 t sexual conflict between individuals in the mating pair.
7 reases in oviposition frequency in zebrafish mating pairs.
8 nts and produces offspring from all possible mating pairs.
9 s cerevisiae, to generate novel, alternative mating pairs.
10 reventing Prm1 transport to contact sites in mating pairs.
11 hat promotes plasma membrane fusion in yeast mating pairs.
12  a mild fusion defect in otherwise wild-type mating pairs.
13 spring viability and reproductive success of mating pairs.
14 with favored males through aggression toward mating pairs.
15 utational workflow that combines paired-end, mate-pair, 10X Genomics linked-read with chromosome conf
16 , assembled de novo with paired-end and long-mate-pair (8 kb) libraries were first assembled and anal
17                                      In some mating pairs, a sudden increase in GFP permeance was fou
18 nsduced to recipients after the formation of mating pairs affects imp activity.
19                                Although fus1 mating pairs also have a defect in degrading the cell wa
20  of array comparative genomic hybridization, mate pair and cloned sequences, and FISH analyses, we ha
21 iguity to discover interchromosomal SVs from mate-pair and pair-end sequencing data.
22 species typically found colonies from single mated pairs and therefore may lack the flexibility to bu
23 ces the cell fusion defect of Prm1-deficient mating pairs and causes a mild fusion defect in otherwis
24 ing high-depth whole genome sequencing of F0 mating pairs and multiple individual F1 offspring, we es
25 d deep-coverage whole-genome (short-insert), mate-pair, and linked-read sequencing as well as karyoty
26                            Obtaining data on mating pairs are difficult for most species; therefore,
27                                              Mating pairs are established in clonal culture via flage
28 e independent functions and only prm1 mutant mating pairs are susceptible to contact-dependent lysis.
29 veals that the two plasma membranes in these mating pairs are tightly apposed, remaining separated on
30      Without Prm1, a substantial fraction of mating pairs arrest with their plasma membranes tightly
31 lished that the F pilus can retract to bring mating pair cells in tight contact before DNA transfer.
32 % is spanned by at least one uniquely placed mate-paired clone.
33 is was reduced in the presence of sufficient mate pair data.
34 an size than constitutional events even when mate-pair data were considered.
35                                              Mate-paired data are used to physically resolve haplotyp
36     We present a model in which members of a mated pair decide whether to care for their offspring or
37                 Using behavioral tracking of mating pairs, deep learning, and quantitative analysis a
38  SMASH combines signals from split reads and mate-pair discordance to detect somatic structural varia
39 wide, next-generation sequencing analysis of mate-pair DNA libraries and applied these tools to 16 PT
40 LCLs lacking ALK translocations, we combined mate-pair DNA library construction, massively parallel (
41 ependent competition that drives assortative mate-pair formation.
42 s and deletions of the DNA processing (dtr), mating pair formation (mpf) and traG coupling genes of R
43 counterattack also occurs in response to the mating pair formation (Mpf) system encoded by broad-host
44 r-recipient interactions, a process known as mating pair formation (MPF).
45 te optimal environments for signal exchange, mating pair formation and widespread lateral gene transf
46                                              Mating pair formation proteins (Trb) from Yersinia pseud
47 sfer and replication system, or Dtr, and the mating pair formation system, or Mpf.
48                   In RP4, these genes encode mating-pair formation functions and are essential for th
49 0, suggesting that these products comprise a mating-pair formation system.
50 adhesins to enhance cellular aggregation and mating-pair formation.
51                                         If a mating pair forms between ergosterol-depleted cells desp
52 arus major) could access food, we restricted mated pairs from being allowed to forage at the same loc
53 d then merged to contigs and scaffolds using mate-pair information.
54 ength of the sequencing reads and absence of mate-pair information.
55 f linking data other than that inferred from mate-pair information.
56 ngth) opens a possibility to transform short mate-pairs into long mate-reads of length approximately
57  wild-type cells, cell fusion in prm1 mutant mating pairs is dramatically reduced when Ca(2+) is remo
58 identified the variants with high complexity mate-pair libraries and a novel computational algorithm
59 lity of contigs and scaffolds using Illumina mate-pair libraries and genetic map information.
60 ssemblies from high-coverage sequencing with mate-pair libraries extending up to 20 kilobases.
61 in a few contigs using only a single Nextera Mate Pair library of short reads.
62                                              Mate pair library sequencing is an effective and economi
63                               In conclusion, mate-pair library generation combined with next-generati
64 n sequencing was performed using an Illumina mate-pair library protocol.
65                                 A cell-free, mate-paired library provided single DNA molecules that w
66 ed the herring genome generating paired-end, mate-pair, linked and long reads.
67    Illumina's recently released Nextera Long Mate Pair (LMP) kit enables production of jumping librar
68                       In its absence, mutant mating pairs lyse or arrest in the mating reaction with
69            Their absence results in frequent mating pair lysis, which is counteracted by Ca(2+)-depen
70       We then carried out massively parallel mate-pair next generation sequencing (NGS) to examine th
71                         The Illumina Nextera Mate Pair (NMP) protocol uses a circularization-based st
72 nce in specificity at either locus between a mated pair of individuals initiates an identical series
73      Long range linking information, such as mate-pairs or mapping data, is necessary to help assembl
74  comprehensive, and integrates read quality, mate pair orientation and insert length (for paired-end
75 adapter site to build 'virtual libraries' of mate pairs, paired-end reads and single-ended reads.
76 ich the production of one female progeny per mated pair per generation has been a rule, several ancie
77                      The correlation between mate-pair PGIs is far too large to be consistent with ph
78         Karyogamy is delayed by >1 h in fus1 mating pairs, possibly as a consequence of retarded fusi
79 1, and Drd2 expression in sexually naive and mate-paired prairie and meadow voles.
80 d by the recently developed Illumina Nextera Mate Pair protocol.
81         In this study we used a whole-genome mate-pair protocol to characterize a landscape of genomi
82                                              Mate pair protocols add to the utility of paired-end seq
83  Unfortunately, the mapping and alignment of mate-pair read pairs to a reference genome is a challeng
84                         However, introducing mate-paired reads (separated by a gap of length, GapLeng
85  novel approach for detecting indels between mate-paired reads that are smaller than the standard dev
86                 We collected several billion mate-paired reads yielding approximately 18x haploid cov
87 6,529 intra-read indels, 5590 indels between mate-paired reads, 91 inversions, and four gene fusions.
88 g one based on read overlaps and paired-end (mate-pair) reads.
89   The high sequence coverage and presence of mate pairs result in fairly long haplotypes (N50 length
90     Electron microscopy of Deltakex2-derived mating pairs revealed novel extracellular blebs at presu
91 thms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform
92      Extra constraints, including gap sizes, mate pairs, scaffold order and orientation, are explored
93      It also demonstrates that high-coverage mate-paired sequence can overcome assembly difficulties
94 by combining shotgun fragment and short jump mate-pair sequences with Hi-C data to generate chromosom
95                  In this study, we performed mate pair sequencing (MPseq) on genomic DNA from 24 PDAC
96                         Through whole-genome mate pair sequencing, we mapped and classified rearrange
97 c alterations of originating tumors based on mate pair sequencing.
98 equencing alignment programs when processing mate pair sequencing.
99  the relationship of histologic populations, mate-pair sequencing (MPseq) and exome sequencing (Exome
100 les the high numbers of artifacts present in mate-pair sequencing and reduces the false positive rate
101 ge test based on genomic rearrangements from mate-pair sequencing demonstrates promise for distinguis
102 focus on regions of gene amplification using mate-pair sequencing of long-insert genomic DNA with mat
103                           By next-generation mate-pair sequencing we have mapped the chromosomal dele
104 gle nucleotide polymorphism (SNP) arrays and mate-pair sequencing-to compare CNVs that occur constitu
105 scribe a new tool, EULER-USR, for assembling mate-paired short reads and use it to analyze the questi
106 methods to reconstruct genomes directly from mate-paired short-read metagenomes.
107 stinct OM receptors in recipients to mediate mating pair stabilization and efficient DNA transfer.
108 fourth TraN structural variant that mediates mating pair stabilization by binding OmpF.
109                Despite the requirement for a mating pair stabilization homologue, static coculture tr
110 ae isolates, demonstrating the importance of mating pair stabilization in mediating conjugation speci
111 homologous protein acts in pilus production, mating pair stabilization, and entry exclusion.
112 l modification in a manner that could affect mate pairing success in birds.
113 s generalize the concept of paired reads, or mate pairs, that have been routinely used for structural
114 s which block mating before the formation of mating pairs, the ste6(cef) (cell fusion) alleles permit
115 iversity of social organization, from simple mated pairs to complex communities of interdependent ind
116        We investigated genotypically similar mating pairs using genome-wide single nucleotide polymor
117 morum, known to be widespread and diverse in mating pairs, was found to encompass all of the isolates
118  in the old macronucleus of one partner of a mating pair were sufficient to inhibit deletion occurrin
119 aintaining ideal acoustic recognition within mating pairs while acoustically masking phonotactic resp
120              Pup survival was not higher for mated pairs with above average heterozygosity in my mode
121                 Finally, I hypothesized that mated pairs with above average heterozygosity would have
122 y about 7% of the number of pups produced by mating pairs with an iPLA(2)beta(+/+) or iPLA(2)beta(+/-
123 sted whether exposure to the visual cue of a mating pair would increase the mating propensity of an o
124                               Lpla2-/- mouse mating pairs yielded normal litter sizes, indicating tha

 
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