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1 ogenesis, and urge consideration of a'second human genome project'.
2 will be addressed using information from the Human Genome Project.
3 rategy has been employed for portions of the Human Genome Project.
4 ld have a high priority in completion of the Human Genome Project.
5 of 300 kb is one of the stated goals of the Human Genome Project.
6 ey rationales, in 1986, for embarking on the human genome project.
7 the development of molecular biology and the Human Genome Project.
8 velopment currently, mainly triggered by the Human Genome Project.
9 s human tyrosyl-tRNA synthetase cDNAs by the Human Genome Project.
10 es represents a critical goal of the ongoing Human Genome Project.
11 100 kbp apart has been a central goal of the Human Genome Project.
12 ntification, one of the central hopes of the human genome project.
13 ens and key model organisms generated by the Human Genome Project.
14 These breakthroughs helped launch the Human Genome Project.
15 yet fall into this unassembled region of the Human Genome Project.
16 MID clones sequenced as part of the original human genome project.
17 s gained momentum with the completion of the human genome project.
18 emains the greatest obstacle confronting the human genome project.
19 ly identified by either Celera or the public Human Genome Project.
20 e 19q13.1 that had not been sequenced by the Human Genome Project.
22 ncing of the long arm of chromosome 7 in the Human Genome Project, a predicted protein product of 40
25 studies with complex disorders in this post Human Genome Project age, and emphasize the importance o
26 he genome sequence framework provided by the human genome project allows us to precisely map human ge
32 ps for a variety of organisms as part of the Human Genome Project and in creating various methods for
33 th use of the latest tools emerging from the Human Genome Project and indicate that future attempts t
36 century, we have seen the completion of the human genome project and marked progress in the human mi
37 act on research in molecular biology, on the human genome project and on the diagnosis of disease.
38 molecular biology, especially as part of the Human Genome Project and other high-throughput DNA seque
39 tion of genetic information generated by the Human Genome Project and related research has heightened
41 ideas were part of the rationale driving the Human Genome Project and subsequently the personalized m
48 The development of resources such as the Human Genome Project and the International Human Haploty
49 isms have been identified as a result of the human genome project and the rapid advance of high throu
51 te of genetic discoveries facilitated by the Human Genome Project and the unprecedented opportunity t
52 in depth, particularly in the context of the Human Genome Project and, to a lesser extent, the propos
55 n genome, and technology improvements by the human genome project are completely transferable, transl
56 n made in recent years, as the fruits of the Human Genome Project are facilitating the identification
58 templates for the sequencing efforts of the Human Genome Project as well as more focused positional
62 in human healthcare that are presaged by the Human Genome Project can be realized by the pharmaceutic
64 ert genomic clones, sequenced as part of the Human Genome Project, comprises a quarter of the genome,
70 ce data quality and genome size early in the Human Genome Project, estimates of protein interaction d
72 of recent advances in biotechnology and the human genome project for disease diagnosis and prognosis
73 the drug discovery horizon, well before the Human Genome Project gave it promise at the turn of the
74 a direct result of tremendous gains from the human genome project, genome-wide association studies, a
76 at the greatest transformative aspect of the Human Genome Project has been not the sequencing of the
95 ion of KLLN, a gene uncovered well after the human genome project, has been linked to Cowden cancer-p
96 Recent progress, accelerated through the Human Genome Project, has resulted in the rapid identifi
97 ar genetic technology and the success of the human genome project have empowered investigators with n
98 technological capabilities emerging from the human genome project have finally reached the point wher
99 cular genetic analysis and completion of the Human Genome Project have sparked a worldwide effort to
100 mparisons, coupled with the resources of the Human Genome Project, have been used to identify pericen
102 quence to the HuRef genome compared with the Human Genome Project (HGP) reference sequence (hg18).
104 t (HMP) is following in the footsteps of the Human Genome Project (HGP), which will include exciting
108 Protein Sequence and Structure' through the Human Genome Project in the late 1990s and early 2000s t
109 s, in what has aptly been called "the second Human Genome Project." In this review we discuss the seq
110 sequences is essential for a variety of post human genome projects including detection of specific ge
117 technologies that have been gained from the Human Genome Project, it has been possible to begin to u
121 oughput sequencing programmes, including the Human Genome Project led to the 'identification' of a la
124 ructural abnormalities and completion of the Human Genome Project, much of the structural variation i
126 source for browsing manual annotation of the human genome project, now contains five reference genome
127 ably similar objections were voiced when the Human Genome Project, now widely viewed as a success, wa
130 ults were conducting research similar to the Human Genome Project (OR, 2.09; 95% CI, 1.75-2.42), publ
132 recent biological revolution, spurred by the human genome project, promises the advent of novel techn
135 search is underway to define those genes.The Human Genome Project provides the basis that allows us t
138 nonredundant human genome sequence from the Human Genome Project-Santa Cruz (HGP-sc; October 2000 an
139 ript map, YAC-to-BAC scaffold, and reference Human Genome Project sequence provides a powerful integr
140 , physical-map positions from the Celera and Human Genome Project sequence, and likelihood-ratio supp
144 ng publicly available sequence data from the human genome project, the 1000 Genomes Project, and The
145 cing of the human genome is completed by the Human Genome Project, the analysis of this rich source o
146 ous organisms and imminent completion of the Human Genome Project, the entire process of discovery in
147 ed in recent years from projects such as the Human Genome Project, the HapMap Project and Genome-Wide
151 rages the recent advances resulting from the Human Genome Project to increase our understanding of bi
152 d on the resources provided by the mouse and human genome projects to help define the tissue interact
153 pic analysis of proteins) with data from the human genome project, to establish a national consortium
155 p from genomic sequence data released by the Human Genome Project, using a seed-and-walk approach.
159 f human genes being sequenced as part of the human genome project, we developed a high-throughput ass
160 ts following closely in the footsteps of the Human Genome Project, which has opened the door to genom
161 ented in which information obtained from the human genome project will aid in the final characterizat
162 challenge of the post-sequencing era of the human genome project will be the functional annotation o
165 el with a large-scale sequencing effort, the human genome project will need next-generation tools for
168 in hamster cells and, with completion of the human genome project, will allow rapid identification of
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