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1 nificant BLASTN hits (E < e(-5)) against the human genome sequence.
2                                  We have the human genome sequence.
3 esent, despite their apparent absence in the human genome sequence.
4 human DNA not yet contained in the available human genome sequence.
5  bands in the June 2002 version of the draft human genome sequence.
6  superfamily ribonucleases identified in the human genome sequence.
7 hese tumors with patterns predicted from the human genome sequence.
8 rrations quantitatively from 14 FTC onto the human genome sequence.
9 o be part of a transcriptional module on the human genome sequence.
10  of 524 sites of HIV cDNA integration on the human genome sequence.
11 l genes from regions of interest using draft human genome sequence.
12  complete the assembly and annotation of the human genome sequence.
13 s and in silico restriction digestion of the human genome sequence.
14 was performed using the draft version of the human genome sequence.
15 osition of having two distinct drafts of the human genome sequence.
16 rgeted, single-copy probes directly from the human genome sequence.
17 ompleted >98 Mb ( approximately 3.3%) of the human genome sequence.
18 international effort to determine a complete human genome sequence.
19 f mirror repeats in the telomere-to-telomere human genome sequence.
20 s to identify all functional elements of the human genome sequence.
21 cessful in mammals, accounting for 30-40% of human genome sequence.
22 ure has been evolutionarily imprinted on the human genome sequence.
23 s of the largest tandem repeats found in the human genome sequence.
24 ds to rigorously analyze a defined 1% of the human genome sequence.
25 n a population with respect to the reference human genome sequence.
26 agreeing with the location at 1p36.22 in the human genome sequence.
27 were located within 1 to 5 Mb based upon the human genome sequence.
28 tive elements collectively occupy 44% of the human genome sequence.
29 to the functional annotation of variation in human genome sequences.
30  their chromosomal locations from the latest human genome sequences.
31  and an expanded set of high-coverage modern human genome sequences.
32 esource to be valuable for the annotation of human genome sequences.
33 e identifiable orthologues in the canine and human genome sequences.
34 le haplotype resolution to become routine in human genome sequencing.
35 nical risk factors has evolved in the era of human genome sequencing.
36 nome draft sequence and the Celera assembled human genome sequence, 36% of the STSs had a discrepant
37 ch sites have been precisely resolved on the human genome sequence(6).
38  human-specific HERV-K(HML2) elements in the human genome sequence, 8 of which are insertionally poly
39                  With further, more accurate human genome sequencing, additional mutation hotspots, m
40               The recent availability of the human genome sequence allowed the identification of thre
41                        The completion of the human genome sequence allows for new ways to analyze glo
42                 The recent completion of the human genome sequence allows genomics research to focus
43       The availability of both the mouse and human genome sequences allows for the systematic discove
44 levels in this family by using the published human genome sequence and a diverse sample of 19 humans.
45 tions utilize information from the completed human genome sequence and a large, high-quality set of h
46                  The availability of a draft human genome sequence and ability to monitor the transcr
47 l know all of the 3 billion DNA bases in the human genome sequence and all of the variations in the g
48 GS patterns with patterns predicted from the human genome sequence and displayed as Virtual Genome Sc
49                   With the completion of the human genome sequence and genome sequence available for
50 we mapped expressed sequences onto the draft human genome sequence and only accepted splices that obe
51                      The availability of the human genome sequence and progress in sequencing and bio
52    It includes 3,658 genes homologous to the human genome sequence and provides a framework for overl
53 very 5 kilobases that is integrated with the human genome sequence and that is freely available in th
54 r (DOP)-PCR can be precisely mapped onto the human genome sequence and that it is possible to predict
55 lted in accelerated plans for completing the human genome sequence and the earlier-than-anticipated i
56 logies, particularly the availability of the human genome sequence and the ongoing sequencing of canc
57  new tools is the availability of the entire human genome sequence and the prospect that within the n
58                              Deciphering the human genome sequence and the publication of the human h
59                      The availability of the human genome sequence and tools for interrogating indivi
60 ersity was estimated from an analysis of six human genome sequences and found to deviate from the exp
61                     The recent completion of human genome sequencing and advances in DNA microarray t
62                         In parallel with the human genome sequencing and assembly effort, many tools
63 Applying this method to data from the Celera human genome sequencing and SNP discovery project, we ob
64 ing oligonucleotide probes designed from the human genome sequence, and hybridizing with "representat
65 identification of transcribed regions in the human genome sequence, and many researchers accept them
66 1) insertions comprise as much as 17% of the human genome sequence, and similar proportions have been
67 nsembl site is one of the leading sources of human genome sequence annotation and provided much of th
68  evolution, yet only a small fraction of the human genome sequence appears to be subject to evolution
69                                     With the human genome sequence approaching completion, a major ch
70         The internet sites that showcase the human genome sequence are blazing a new trail.
71 NA variation and archival information on the human genome sequence are now readily available.
72                       Now that the mouse and human genome sequences are complete, biologists need sys
73              Using current approaches, whole human genome sequences are not typically assembled and d
74 most recent mouse, rat, dog, chimpanzee, and human genome sequence assemblies to compile a near-compl
75 sis of homology between mouse Sycp3 cDNA and human genome sequences at the aminoacid level.
76 er throughput nanopore sequencers, mean that human genome sequencing at scale is now possible.
77                   With the completion of the human genome sequence, attention turned to identifying a
78  will be increasingly valuable as additional human genome sequences become available.
79 ge for DNA sequencing remains great, despite human genome sequences being 99.5% identical, the 3 mill
80  fields through the production of a complete human genome sequence, but also had driven the developme
81 ave revolutionized biology by completing the human genome sequence, but in the race to completion we
82 ill be required to obtain the 3-billion-base human genome sequence by the target date of 2005.
83 h the goal of completing the first reference human genome sequence by the year 2005.
84 ith flanking regions among the ~186 thousand human genomes sequenced by the TOPMed project.
85 estigators at the Baylor College of Medicine Human Genome Sequencing Center (BCM-HGSC) and BeeBase or
86  generated at the Baylor College of Medicine Human Genome Sequencing Center were compared with the hu
87 cus genome at the Baylor College of Medicine Human Genome Sequencing Center, the average success rate
88  throughput genomic sequences from the major human genome sequencing centers.
89 ge repository of the data being generated by human genome sequencing centers.
90 and graph sizes with an increasing number of human genome sequences compared to Bifrost and variation
91 rtant implications for efforts to finish the human genome sequence, complicates comparative sequence
92      Alignments of the RH map to macaque and human genome sequences confirm a large inversion and rev
93 e human genome assembly by the International Human Genome Sequencing Consortium (HGSC) and Celera Gen
94 cted gene sets produced by the International Human Genome Sequencing Consortium (HGSC) and Celera Gen
95 me sequencing performed by the International Human Genome Sequencing Consortium (IHGSC) and Celera Ge
96                       When the International Human Genome Sequencing Consortium (IHGSC) published its
97                            The International Human Genome Sequencing Consortium (IHGSC) recently comp
98                            The International Human Genome Sequencing Consortium constructed a map of
99 aft human genome sequence, the International Human Genome Sequencing Consortium has proceeded to fini
100 ed genome was published by the International Human Genome Sequencing Consortium in 2004.
101 lysis of clone overlaps by the International Human Genome Sequencing Consortium.
102                                The published human genome sequence contains many thousands of endogen
103                                    Thus, the human genome sequence contains signatures for chromatin
104 ttle-human comparative map was created using human genome sequence coordinates of the paired ortholog
105  comparative anchor loci is 1.15 Mb based on human genome sequence coordinates.
106                        The completion of the human genome sequence, coupled with the imminent complet
107 integrated information from the most current human genome sequence data (UCSC genome assembly Human J
108 bling the generation of massive compendia of human genome sequence data and associated molecular and
109 sferase, identified by BLAST searches of the human genome sequence data base, has been cloned, expres
110 ith these techniques, a 45x coverage of real human genome sequence data compresses losslessly to unde
111                     Due to the large size of human genome sequence data files (varying from 30 GB to
112 ome that accounts for 96.8% of the available human genome sequence data.
113 p encompassing the 300-kb deletion using the human genome sequence database and confirmed the map usi
114 sm (SNP) markers is to take advantage of the human genome sequencing effort currently under way.
115 und in the world-wide population revealed by human genome sequencing efforts and the highly variable
116                                              Human genome sequencing efforts have greatly expanded, a
117          On the basis of identical mouse and human genome sequences encoding the autophosphorylation
118                           In interphase, the human genome sequence folds in three dimensions into a r
119 arched the proteins predicted from the draft human genome sequence for paralogues of known tumour sup
120                              A search of the human genome sequences for proteins with a COOH-terminal
121 scalability of this platform enable complete human genome sequencing for the detection of rare varian
122           Alignment of human tauCstF-64 with human genome sequence from chromosome 10 shows that CSTF
123 , we analyzed approximately 300 kilobases of human genome sequence from diverse gene loci and cleanly
124 , on the basis of the assembled nonredundant human genome sequence from the Human Genome Project-Sant
125 t can: (i) retrieve any particular region of human genome sequence from the NCBI database and (ii) an
126                 The availability of complete human genome sequences from populations across the world
127  identification from finished and unfinished human genome sequence has become critically important in
128                                          The human genome sequence has been finished to very high sta
129                     The determination of the human genome sequence has brought these metaphors to the
130                      The availability of the human genome sequence has enabled the exploration and ex
131                 The recent completion of the human genome sequence has enabled the identification of
132                       The deciphering of the human genome sequence has enabled the identification of
133             The availability of the complete human genome sequence has highlighted the need for a too
134                              Analysis of the human genome sequence has identified approximately 25000
135                            Completion of the human genome sequence has inspired a new wave of epidemi
136                       The elucidation of the human genome sequence has made it possible to identify g
137                      The availability of the human genome sequence has opened up the possibility of i
138                                          The human genome sequence has profoundly altered our underst
139                          The availability of human genome sequence has transformed biomedical researc
140                                              Human genome sequencing has transformed our understandin
141                             Personal diploid human genome sequences have been generated, and each has
142  and challenges that the availability of the human genome sequence holds for cancer research.
143  of Single Nucleotide Polymorphisms (dbSNP), Human Genome Sequencing, Human MapViewer, GeneMap'99, Hu
144  of Single Nucleotide Polymorphisms (dbSNP), Human Genome Sequencing, Human MapViewer, Human inverted
145                              A search of the human genome sequence identified the vWF-cleaving protea
146 retation of the information contained in the human genome sequence in terms of the structure, functio
147                                            A human genome sequenced in only an hour is likely to beco
148           There has been a rapid increase in human genome sequencing in the past two decades, resulti
149                                 The reported human genome sequence includes about 400 gaps of unknown
150 ens of millions of base pairs of euchromatic human genome sequence, including many protein-coding gen
151                                The wealth of human genome sequence information now available, coupled
152                            Over one-third of human genome sequence is a product of non-LTR retrotrans
153                                    The draft human genome sequence is an important step in cataloguin
154                           Now that the draft human genome sequence is available, everyone wants to be
155                              About 5% of the human genome sequence is composed of the remains of retr
156                             Variation in the human genome sequence is key to understanding susceptibi
157                     A 'working draft' of the human genome sequence is now available.
158                                              Human genome sequencing is accelerating rapidly.
159                              The progress of human genome sequencing is driving genetic approaches to
160                          Although individual human genome sequencing is increasingly routine, nearly
161                                              Human genome sequencing is routine and will soon be a st
162             With recent access to the entire human genome sequence, it has become possible and highly
163 tant resource for genomic research after the human-genome sequence itself, yet the major gene catalog
164                      The availability of the human genome sequence led us to propose that systematic
165 an genetic variation that will come from the human genome sequence makes feasible a polygenic approac
166                         In majority of them, human genome sequences matched exactly the reverse-compl
167 us effort committed to the annotation of the human genome sequence, most notably perhaps in the form
168                                     With the human genome sequence nearing completion, new opportunit
169        The mouse contigs were aligned to the human genome sequence on the basis of 51,486 homology ma
170  demonstrate application of this approach to human genome sequencing on flow-sorted X chromosomes and
171 ith the completion of a draft version of the human genome sequence only a fraction of the genes ident
172  of Single Nucleotide Polymorphisms (dbSNP), Human Genome Sequencing pages, GeneMap'99, Davis Human-M
173 cation in the final stages of completing the Human Genome Sequencing Project and in applications of B
174  the DNA database arising as a result of the human genome sequencing project enabled us to identify A
175                           The success of the human genome sequencing project has created wide-spread
176                        The completion of the human genome sequencing project has provided a flood of
177                        There are a number of human genome sequencing projects worldwide that have res
178 s (PACs) have proved excellent tools for the human genome sequencing projects.
179 witnessed an explosion of successful ancient human genome-sequencing projects, with genomic-scale anc
180                                          The human genome sequence provides a reference point from wh
181                                 The finished human genome sequence provides a thorough catalog of the
182 ex approximately 3.6 million DHSs within the human genome sequence, providing a common coordinate sys
183 everal advances, including completion of the human genome sequence, publication of genome sequences f
184 lera Genomics produced working drafts of the human genome sequence, published in 2001, but refinement
185 ds that contain a provirus are mapped to the human genome, sequence reads that cannot be localized to
186                        Interpretation of the human genome sequence relies on studies of model genetic
187                                          The human genome sequence remains incomplete, with multimega
188                         Clinical adoption of human genome sequencing requires methods that output gen
189 ent of differentially expressed genes to the human genome sequence resulted in a larger number of gen
190   Analysis of these clones and search of the human genome sequence revealed an uncharacterized group
191 he initial analysis of the draft copy of the human genome sequence revealed the presence of several g
192  the recently published essentially finished human genome sequence reveals several thousand undocumen
193                                The reference human genome sequence set the stage for studies of genet
194 nomic sequence we obtained and the reference human genome sequence share a most recent common ancesto
195                              Analysis of the human genome sequence shows the presence of genes encodi
196                   However, findings from the human genome sequence suggest an unprecedented degree of
197 Cebus albifrons) and from the chimpanzee and human genome sequences, suggests that this is the genera
198                              Our analyses of human genome sequences syntenic to these regions suggest
199                                Can the draft human genome sequence tell us how the cell cycle works a
200 l search for new viruses in some of the many human genome sequences that are now available thanks to
201 ed by MEDCO is a $10 million prize for whole human genome sequencing that will test 100 samples and e
202              After the completion of a draft human genome sequence, the International Human Genome Se
203                              With a match to human genome sequences, the approximate location of a qu
204                   With the accomplishment of human genome sequencing, the number of sequence-known pr
205   In a large-scale retrospective analysis of human genome sequences, this profile score was shown to
206  comparing their flanking sequences with the human genome sequence; this enabled conserved segments b
207  yield the functional elements buried in the human genome sequence, thus helping to annotate non-codi
208 mpared with the best matching regions of the human genome sequence to assay the amount and kind of DN
209 ficial chromosome (BAC) clones and the draft human genome sequence to complete a contiguous string of
210  and provides a framework for overlaying the human genome sequence to the mouse and for sequencing th
211 ing in run time of only a few hours on whole human genome sequenced to the depth of 20X, for both ver
212                                  For diploid human genomes sequenced to 30x HiFi coverage, HiCanu ach
213                      The availability of the human genome sequence together with sequenced genomes of
214 apping expressed sequence tags (ESTs) to the human genome sequence using a binary indexing algorithm.
215 and all mRNA sequences were aligned with the human genome sequence using LEADS, Compugen's alternativ
216 uencing technology development; for studying human genome sequence variation; for developing technolo
217                      Taking advantage of the human genome sequence, we have performed extensive seque
218        With the availability of the complete human genome sequence, we performed a comprehensive anal
219                           Using the compiled human genome sequence, we systematically cataloged all t
220  as potential therapeutic targets, drafts of human genome sequence were interrogated.
221     The potential threat is evident from the human genome sequence, which reveals many past epidemics
222  in 2001, but refinement and analysis of the human genome sequence will continue for the foreseeable
223                             Knowledge of the human genome sequence will enable us to understand how t
224                         Information from the human genome sequence will eventually alter many aspects
225                                 The complete human genome sequence will facilitate the identification
226                           We discuss how the human genome sequence will further our understanding of
227                                          The human genome sequence will provide a reference for measu
228 ron structures of genes in finished or draft human genome sequence with a low rate of false-positives
229                             Investigation of human genome sequences with a consensus sequence derived
230 source of stable automatic annotation of the human genome sequence, with confirmed gene predictions t

 
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