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1 inst authenticate published ITS sequences in GenBank.
2 390 full-length human HCV 1a sequences from GenBank.
3 ifies itself and nothing else in a search of GenBank.
4 lar to any genes with annotated functions in GenBank.
5 y annotation namespaces, e.g. KEGG or NCBI's GenBank.
6 ing for the deposition of 4,850 sequences to GenBank.
7 uated by testing from 27 to 240 genomes from GenBank.
8 capsid sequence from 56 strains available in GenBank.
9 up of randomly selected Ig heavy chains from Genbank.
10 ions were stable across successive builds of GenBank.
11 cs sites and community data archives such as GenBank.
12 the cloned fragments with the nr-database in Genbank.
13 en the compared RH1 sequences and those from GenBank.
14 t GenBank table files prior to submission to GenBank.
15 nces were identified, 3 of which were not in GenBank.
16 he 11 complete genome sequences available in GenBank.
17 g maize DNA sequences currently available in GenBank.
18 ster virus have been published and listed in GenBank.
19 l databases, such as EntrezGene, UniProt and GenBank.
20 All known sequences were extracted from GenBank.
21 at the protein level with other sequences in GenBank.
22 um, and its sequences have been deposited in GenBank.
23 (UniProt) and the associated mRNA data from Genbank.
24 otein that has no apparent homologues within GenBank.
25 454 technology, but that lacked orthologs in GenBank.
26 is maintained in collaboration with DDBJ and GenBank.
27 The sequences have been deposited in GenBank.
28 were carried out with sequences deposited in GenBank.
29 the common files required for submission to GenBank.
30 a clonal activating point mutation in HRAS (GenBank 3265) (c.37G-->C) in the Spitz nevi and underlyi
35 C (GenBank accession no. AY589511) and XTES (GenBank accession no. AY989815), which are closely relat
37 as an environmental stress-responsive gene (GenBank accession number AL049644.1, locus spcc191.01).
38 novel human PKCdelta isozyme, PKCdeltaVIII (Genbank accession number DQ516383) in human teratocarcin
40 K14-vGPCR/ORF74 mRNA, terminating at 130873 (GenBank accession number GQ994935), resulting in an appr
41 herin 15 CD3 pointed to amino acids 158-179 (GenBank accession number XP_238200), with homology to th
43 ers for the gene(s) of interest, such as by: GenBank accession number, NCBI protein accession number,
44 tently matched to B. anthracis plasmid pX02, GenBank accession numbers AF188935.1, AE011191.1, and AE
45 ne abstracts using sequence ID lists such as GenBank accession numbers derived from high-throughput e
47 are referenced by clone numbers or 16S rRNA GenBank accession numbers, often without taxonomic ancho
48 ther identifiers, such as specimen codes and GenBank accession numbers, to link otherwise disconnecte
58 of a Lingulodinium EST dataset deposited in GenBank and 94% of the enzymes in 16 primary metabolic K
59 he species and sequences present in the NCBI GenBank and allows for a single step classification of m
62 orted at this position in all mammals in the GenBank and Ensembl databases, with arginine reported in
64 plished by querying public databases such as GenBank and examining the geospatial metadata in the rec
68 Entrez database, Entrez Nucleotide, includes GenBank and is tightly linked to the NCBI Taxonomy datab
77 ysis and retrieval resources for the data in GenBank and other biological data available through NCBI
78 ysis and retrieval resources for the data in GenBank and other biological data made available through
79 ysis and retrieval resources for the data in GenBank and other biological data made available through
80 ysis and retrieval resources for the data in GenBank and other biological data made available through
81 ysis and retrieval resources for the data in GenBank and other biological data made available through
82 ysis and retrieval resources for the data in GenBank and other biological data made available through
94 quences reported in this study) available in GenBank and reported from 23 countries were characterize
97 aking advantage of the exponential growth of GenBank and the creation of NCBI's RefSeq database, we h
98 because of the large number of sequences in GenBank and the large number of highly similar paralogue
99 0 complete bacterial genomes and plasmids in GenBank and were capable of detecting 82% of the ISs and
100 pared to all complete sequences available in GenBank, and haplotype analysis demonstrated 92 haplotyp
101 tent with the corresponding information from GenBank, and produced better performance compared to exi
102 on, 3615 genome sequences occupying 56 MB in GenBank are compressed down to only 167 KB, achieving a
106 seen R and the Gene Ontology join BLAST and GenBank as the main components in bioinformatics process
107 rresponding to a gene currently annotated in Genbank as TSGA2 homolog (mouse) to signify 'testis spec
108 0% of cDNA and mRNA sequences contributed to GenBank before the patent application was filed also con
110 corrected sample dates modified by others in GenBank but also corrected an additional transcriptional
112 hic Alu insertions in sequences submitted to GenBank by screening the elements against reference geno
113 that can be used for sequence submission to GenBank (by Sequin or tbl2asn), a GenBank flat file, or
115 n this study combined with 339 obtained from GenBank), collected from patients in 36 provinces in Vie
117 <30% of the prokaryotic genomes submitted to GenBank contain partial repeat features of specific type
118 arly in the context of missing or incomplete GenBank data, and, whenever possible, should be evaluate
120 ces of the circulating HIV-1 isolates in the GenBank database and observed that, in addition to the p
131 More than 97% of HBV BCP sequences in the GenBank database can be correctly identified by the melt
132 ional Center for Biotechnology Information's GenBank database is problematic because of annotation er
133 a strain of M. catarrhalis available in the GenBank database was analyzed, and open reading frames p
140 einhardtii expressed sequence tags (ESTs) in GenBank dbEST and community EST assemblies were either o
142 ore, legacy bioinformatics file formats like GenBank do not provide enough information about the purp
143 e data from this article can be found in the GenBank/EMBL data libraries under accession numbers BE 6
144 e data from this article can be found in the GenBank/EMBL data libraries under accession numbers DU 6
145 from this study have been submitted to DDBJ/GenBank/EMBL under accession numbers EU940701-EU977132 (
149 E products for antisense transcripts and the GenBank EST database revealed that TART antisense transc
150 European Molecular Biology Laboratory (EMBL)/GenBank feature table format for reading and displaying
154 hical user interface, validation of uploaded GenBank files, and abilities to import phages from exist
156 gene annotation and DNA sequence data from a GenBank flat file, (ii) displaying patterns of gene cons
157 mission to GenBank (by Sequin or tbl2asn), a GenBank flat file, or the predicted protein sequences in
159 rms, most likely because 70% of the mRNAs in GenBank for these genes were cloned from tumor samples.
160 the MG1655 Genbank record, one of only a few Genbank genome records that are updated by a community e
161 gy Information, comprises a set of duplicate Genbank genome records that can be modified by the NCBI
164 NREF, PIR, Gene Ontology, KEGG, Entrez Gene, GenBank, GenPept, IMAGE, RefSeq, UniGene, OMIM, PDB, Euk
165 y method of loading in sequence files (EMBL, GenBank, GFF) as well as data from relational databases,
166 divergent regions are identical between the GenBank H. taimen and two lenok subspecies, B. lenok and
168 1.89 to 8.68, were further confirmed in 163 GenBank HBV-HCC sequences from nine Asia regions, assaye
170 proportions of sequences without significant Genbank homology, which has hampered identification of v
172 demonstrating that the gene encoding Q5LIW1 (GenBank ID YP_209877.1) was able to complement an API-de
174 ly sequenced plastomes together with 12 from GenBank in an attempt to reconstruct deep relationships
191 c reference for resources such as PubMed and GenBank, it has grown to its current size of >1300 title
193 his particular four-amino acid region, GPPT (GenBank KC329849) versus DLQL (GenBank NC004293), respec
196 sets such as the nucleotide database in NCBI GenBank, metagenomic datasets in Camera, and the marine
198 vel promoters we looked into other evidences-GenBank mRNAs, spliced ESTs, CAGE promoter tags and mRNA
199 region, GPPT (GenBank KC329849) versus DLQL (GenBank NC004293), respectively at residues 389-392.
200 omenclature based on the longest transcript (GenBank: NM_001128227), which encodes a 31-amino acid lo
202 .Arg1173Leu), and c.3008G>A, (p.Gly1003Asp) (GenBank: NM_001273.3), affect evolutionarily highly cons
203 identified two homozygous variants in SPARC (GenBank: NM_003118.3; c.497G>A [p.Arg166His] in individu
204 r protein than the originally described one (GenBank: NM_005476), which has been used previously in m
205 osyl-oligosaccharide glucosidase) mutations (GenBank: NM_006302.2; c.[65C>A; 329G>A] p.[Ala22Glu; Arg
206 ividuals had a homozygous c.692dup mutation (GenBank: NM_022167.3) in the xylosyltransferase II locus
211 expressed sequences collected from the NCBI GenBank Nucleotide database for the construction of tran
215 ving all genomic DNA sequences from the NCBI GenBank, over 1 x 10(11) base pairs of 3.3 x 10(6) seque
216 iales are probably divergent bicoeceans (the GenBank Placidia sequence is a basidiomycete/heterokont
217 f the participating databases, DDBJ, ENA and GenBank, principles of data exchange within the collabor
218 utative environmental peritrich sequences at Genbank, produced a comprehensive tree of peritrichs fro
219 selected taxonomic group have accumulated in GenBank, PUmPER automatically extends the alignment and
232 ry three-marker analysis including taxa from GenBank raises this number to 107 species from 48 genera
233 + links each pseudoknot in PseudoBase to the GenBank record of the corresponding nucleotide sequence
234 source of annotation updates for the MG1655 Genbank record, one of only a few Genbank genome records
235 ana barcode sequences (n = 247, including 24 GenBank records) formed a monophyletic lineage separate
237 he only published IL-10 sequence existing in Genbank reported from C4D guinea pigs, genomic DNA was i
240 1 CGs (30 CGs from our study and 48 CGs from GenBank) revealed two HPV11 lineages (lineages A and B)
241 T similarity (E-value <10-5) to sequences in GenBank's non-redundant databases, indicating that a lar
242 nclature variation and paralogues; moreover, GenBank's structure and tools are not conducive to searc
244 arity to published sequences in unrestricted GenBank searches, and there are no significant open read
245 .4 strains identified in this study and from GenBank segregated these viruses into at least 9 distinc
247 ragments between the donor and the recipient GenBank sequence suggests that the introgression is loca
250 Malo, Tanna, and Epi and compared them with GenBank sequences to determine (i) the distribution of P
252 ded sequences and the sequences deposited in GenBank showed plausible misidentifications, and the use
253 ples, and other mammalian cells available in GenBank showed the predominance of a specific structure
255 ed BankIt or standalone Sequin programs, and GenBank staff assign accession numbers upon data receipt
256 ed BankIt or standalone Sequin programs, and GenBank staff assign accession numbers upon data receipt
257 e sequencing projects into 18 divisions, and GenBank staff assign unique accession.version identifier
258 ed BankIt or standalone Sequin programs, and GenBank staff assigns accession numbers upon data receip
266 sequences were mined from EST databases and GenBank submissions from four insect orders: Coleoptera
268 gnificant homology with proteins reported in GenBank, suggesting that the genus Emaravirus evolved fu
269 logenies built from 2.6 million sequences in GenBank suggests that signal is strong in vertebrates an
272 ms were twice as likely to be represented in GenBank than their normal tissue-associated splice forms
274 n to displaying the original annotation from GenBank, the CMR makes available secondary automated str
276 ious name for nitronate monooxygenase in the GenBank(TM) and PDB databases, but the enzyme was not ki
278 n more than 490 hypothetical proteins in the GenBank(TM), the vast majority of which are currently mi
279 s and validated complete coding sequences in GenBank to (1) regroup the individual probes into consis
280 s full genomes of influenza A available from Genbank to provide an auto-updating documentation of the
281 e alignment tool that generates contigs from GenBank trace file data and BioExtract Server, a web-bas
282 equence Database(http://www.ncbi.nlm.nih.gov/genbank/TSA.html) under accession numbers JI163767-JI182
284 data from this study have been submitted to GenBank under accession numbers: CK329321-CK334090; CF89
286 eptides from other Conus species recorded in GenBank, we date the major duplication events after the
287 with the non-redundant set of corn mRNAs in GenBank, we estimate that there are about 50,000 differe
288 risons with available DNA sequence data from GenBank, we estimate the number of species-level genetic
290 th 332 Chinese HRSVB sequences obtained from GenBank were analyzed to determine the geographic and ye
292 ther with 766 HRSV sequences downloaded from GenBank, were analyzed to understand the recent circulat
293 e a novel gene, OSTL (annotated as RNF217 in Genbank), which shares the first exon and a CpG island w
294 reviously existing R. reniformis sequence in GenBank, while the RN_VAR2 sequence is more divergent.
298 n this work we utilized A-B PCR and screened GenBank with sequences from isolated clones to identify
299 om putative thylacine mitochondrial genes in GenBank, with one of our samples originating from a dire
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