ライフサイエンスコーパス: sequence-tagged site

1 q11 and were analyzed with a large number of sequence tagged sites.

2 rived artificial chromosomes, cosmids and 24 sequence-tagged sites.

3 ISH with 19 YACs, and PCR using 25 different sequence-tagged sites.

4 newly cloned polymorphic markers and 37 new sequence-tagged sites.

5 /BAC contig covering 2p15-p16, a total of 55 sequence-tagged sites (25 of which are polymorphic), inc

6 viously unmapped expressed sequence tags and sequence tagged sites (350) were mapped to chromosomes.

7 Using the sequence tagged site-amplification mapping approach, we

8 An approach termed sequence tagged site-amplification mapping has been impl

9 The 12q14 amplicon was characterized using sequence tagged site-amplification mapping with DNA from

10 Sequence tagged site-amplification mapping, an approach

11 nding yeast artificial chromosome clones and sequence-tagged site analysis suggested that one of the

12 Twenty-one sequence-tagged sites and ESTs from the corresponding hu

13 with 192 YACs and markers including 90 STSs (sequence-tagged sites) and 50 hybridization probes.

14 Sequence tagged sites are being used to anchor cosmids a

15 In addition, 23 new sequence-tagged sites are described that further increas

16 We identified 10 informative sequence-tagged sites associated with 23 polymorphisms o

17 of chromosome 12 retained was determined by sequence tagged site-based PCR analysis.

18 f molecular markers in Drosophila by using a sequence tagged site-based physical map of the genome.

19 A yeast artificial chromosome sequence-tagged site-based (YAC/STS) physical map of 22.

20 n of the rice sequence to a detailed sorghum sequence-tagged site-based genetic map.

21 tematic comparative sequencing of Y-specific sequence-tagged sites by denaturing high-performance liq

22 A4, D2S105, and GATA52A04) was determined by sequence tagged site content mapping of bacterial artifi

23 tly and time-consuming steps associated with sequence tagged site content mapping such as sequencing,

24 by fluorescent in situ hybridization and/or sequence tagged site content.

25 By sequence-tagged site content analysis and long range map

26 46 cM by combining the results of FISH with sequence-tagged site content mapping using data from the

27 to D8S541, was constructed and confirmed by sequence-tagged site content mapping using microsatellit

28 Our sequence-tagged site-content map of chromosome 12 is now

29 evaluated by both a PCR method that involved sequence-tagged site-content mapping of a deletion of TN

30 nome Project, we have constructed a complete sequence-tagged site contig map of chromosome 7, using a

31 hybridization, and identity to a known human sequence-tagged site (D6S2114), was used to map the CITE

32 using fluorescence in situ hybridization and sequence-tagged site database analyses, we also show tha

33 Included in the contig are 11 sequence-tagged sites derived from P1 and cosmid ends.

34 Sequence-tagged sites developed from 19 islet cDNAs were

35 with molecular tools such as locus-specific sequence-tagged site DNA markers and bacterial artificia

36 proximately 4-Mb ordered clone contig map of Sequence tagged sites, expressed sequence tags (ESTs), a

37 the contents of available genomic sequences, sequence tagged sites, expressed sequence tags, protein

38 Among the sequence tagged site/expressed sequence tag/gene markers

39 A cluster of sequence-tagged sites failed to amplify in an individual

40 uencing framework clones to generate 407 new sequence-tagged sites, followed by PCR verification of o

41 th one or more overgos, which are serving as sequence-tagged sites for single nucleotide polymorphism

42 of the translocation breakpoints using known sequence tagged sites from chromosome 4 and then, after

43 A sequence-tagged site from the candidate gene is used to

44 ers in the region along with newly developed sequence-tagged sites from radiation-reduced hybrids, po

45 We developed sequence-tagged sites from the ends of these BACs and us

46 c microsatellite repeat markers and 17 novel sequence-tagged sites from the region are also described

47 mple tandem repeat DNA polymorphisms, and 14 sequence-tagged sites have been ordered.

48 (ESTs) or UniGenes, 24 polymorphisms, and 56 sequence-tagged sites) have been mapped.

49 ssed sequence tags, 12 polymorphisms, and 97 sequence-tagged sites) have been mapped.

50 is evaluated by comparing predicted to known sequence tagged sites in the human genome.

51 reviously mapped genes, microsatellites, and sequence-tagged sites in the same haploid panel.

52 RAD51C includes a previously mapped sequenced-tagged site location near the end of chromosom

53 c acids or genomes, including hybridization, sequence tagged site mapping, restriction enzyme fingerp

54 Sequence-tagged site mapping places cPLA2beta on chromos

55 Sequence-tagged site mapping places cPLA2gamma on chromo

56 rom 12 populations, we used a combination of sequence-tagged site mapping, and binary-marker and Y-sh

57 the process primarily depended on the HGP's sequence-tagged site maps, BAC maps, and clone-based seq

58 demonstrated that sciellin is linked to the sequence tagged site marker WI-457 with a logarithm of t

59 , we mapped DLG3 to Xq13.1 and established a sequence-tagged site marker map of the surrounding regio

60 13q12.3-q13, approximately 1000 kb from the sequence-tagged site marker WI-3374.

61 2 amplification using quantitative PCR at 11 sequence tagged site markers neighboring the cloned frag

62 was organized to develop and map gene-based sequence tagged site markers on a set of two radiation h

63 ne content of these loci, facilitated by the sequence-tagged site markers and maps of these regions,

64 We quantified copy number of sequence-tagged site markers at 42-550 kb intervals alon

65 l map of the genomic region spanning between sequence-tagged site markers D16S518 and D16S516.

66 ysis of various microcell hybrid clones with sequence-tagged site markers indicates that the metastas

67 The process of converting RAPD markers to sequence-tagged site markers was initiated: 18 RAPD mark

68 reakpoint localizes to two intervals between sequence-tagged site markers, 550 kb and 160 kb in size,

69 hybrid was determined by a PCR analysis with sequence-tagged site markers, and this analysis placed t

70 ome (BAC) clones mapped by our laboratory to sequence-tagged site markers.

71 re confirmed by the identification of mapped sequence-tagged site markers.

72 ell as 69 genes, transposon insertion sites, sequence-tagged sites, microsatellites, and amplified fr

73 an chromosome 5, band q31, incorporating 175 sequence tagged sites, of which 33 are genetic polymorph

74 We have mapped 1001 novel sequence-tagged sites on human chromosome 14.

75 clones, pulse-field gel electrophoresis, and sequence-tagged-site PCR.

76 We used sequence-tagged site polymorphisms to examine the distri

77 Genetic markers consisted of sequence-tagged sites, primarily detected as dCAPS or CA

78 Some of these data were reduced to sequenced tagged site primer sets, facilitating the isol

79 10 clones was constructed across 6q26-q27 by sequence-tagged site/probe content mapping.

80 homologies, single nucleotide polymorphisms, sequence-tagged sites, radiation hybrid data, transposon

81 The mapping results of sequence-tagged sites relative to the two breakpoints we

82 Analyses of sequence tagged site (STS) content and haplotype sharing

83 Clones were assembled by sequence tagged site (STS) content using the five polymo

84 Sequence tagged site (STS) content, restriction fingerpr

85 tificial chromosomes (YACs) and 100 kb inter-sequence tagged site (STS) distance.

86 on the integration of diverse data including sequence tagged site (STS) marker content, clone sizing,

87 Using sequence tagged site (STS) markers flanking L-MYC, incre

88 ybridization using two P1 genomic clones for sequence tagged site (STS) markers, D4S400 and D4S409, w

89 tificial chromosome (BAC) clones anchored to sequence tagged site (STS) markers.

90 Using sequence tagged site (STS)-content mapping and chromosom

91 Sequence tagged sites (STS) and polymorphic markers were

92 de coding regions, conserved domains, tRNAs, sequence tagged sites (STS), variation, references, gene

93 Sequence-tagged site (STS) content mapping in yeast arti

94 A PCR-based sequence-tagged site (STS) content mapping strategy has

95 By sequence-tagged site (STS) content mapping, we roughly d

96 o a physical map of the region by PCR-based, sequence-tagged site (STS) content mapping.

97 We generated a sequence-tagged site (STS) from the derived sequence out

98 The map includes 30 genes, four sequence-tagged site (STS) loci, and 10 DNA markers.

99 cation of these models with 10 chromosome 17 sequence-tagged site (STS) markers and the thymidine kin

100 sion has been tested for the retention of 39 sequence-tagged site (STS) markers by the polymerase cha

101 p of each human chromosome with a density of sequence-tagged site (STS) markers exceeding one every 1

102 mily with ADC and a panel of polymorphic DNA sequence-tagged site (STS) markers for known ADC loci an

103 We utilized a number of sequence-tagged site (STS) markers from 12q24.1 to scree

104 Sequence-tagged site (STS) markers were generated from s

105 ap spanning 88 centirays with 8 genes and 15 sequence-tagged site (STS) markers.

106 ed using publicly available mapping data and sequence-tagged site (STS)-based PCR confirmation.

107 A combination of chromosome walking and sequence-tagged site (STS)-content mapping resulted in a

108 ng a yeast artificial chromosome (YAC)-based sequence-tagged site (STS)-content mapping strategy, 215

109 hysical map spanning CTNS was constructed by sequence-tagged site (STS)-content mapping.

110 An acceptable sequence-tagged site (STS)-PCR assay yielded the appropr

111 eviously published contigs provides complete sequence-tagged site (STS)/YAC-based coverage of the lon

112 Nine new sequence-tagged sites (STS) are also characterized from

113 raploid (AtDt) Gossypium genomes composed of sequence-tagged sites (STS) that foster structural, func

114 e markers D6S1253-D6S295, and have mapped 43 sequence-tagged sites (STS) within this interval.

115 d for identification of novel human or mouse sequence tagged sites (STSs) from contigs of genomic clo

116 netic markers, 5 new polymorphic markers, 57 sequence tagged sites (STSs) generated from PAC end frag

117 AC contig of this region identified multiple sequence tagged sites (STSs) present at both BP2 and BP3

118 he 13q YAC-cosmid map was annotated with 655 sequence tagged sites (STSs) with an average spacing of

119 ure that is used to search DNA sequences for sequence tagged sites (STSs), each of which is defined b

120 (RPCI-23) BAC library, using known genes and sequence tagged sites (STSs).

121 cific backcross panels to map genetically 30 sequence-tagged sites (STSs) and 13 genes to the vicinit

122 with another 22 YACs confirming the order of sequence-tagged sites (STSs) and position of YACs on the

123 Human Genome Project was the decision to use sequence-tagged sites (STSs) as common landmarks for gen

124 gies were devised to identify PCR-detectable sequence-tagged sites (STSs) at introns.

125 , genes, expressed sequence tags (ESTs), and sequence-tagged sites (STSs) compared to any other genom

126 We have developed 338 sequence-tagged sites (STSs) containing (CAG/CTG)n repea

127 s (the TNG panel) in conjunction with 40,322 sequence-tagged sites (STSs) derived from random genomic

128 tanford G3 panel) in conjunction with 10,478 sequence-tagged sites (STSs) derived from random genomic

129 Fifty-four sequence-tagged sites (STSs) developed from BAC insert e

130 NPs) were discovered via the resequencing of sequence-tagged sites (STSs) developed from expressed se

131 Sequence-tagged sites (STSs) from these YACs have been u

132 Human DNA-specific sequence-tagged sites (STSs) have been developed from 19

133 P1 artificial chromosome (PAC) clones using sequence-tagged sites (STSs) mapped to the YAC contig, A

134 ication step, making it necessary to develop sequence-tagged sites (STSs) that amplify only the DNA f

135 By examining a number of sequence-tagged sites (STSs) that span several megabases

136 a collection of 2,848 SNPs located in 1,755 sequence-tagged sites (STSs) using high-density oligonuc

137 onto which 25 polymorphic and nonpolymorphic sequence-tagged sites (STSs) were placed in a unique ord

138 Using sequence-tagged sites (STSs) within the region, a total

139 fic and sensitive PCR provides the basis for sequence-tagged sites (STSs), unique landmarks that have

140 evenly across the map were used to generate sequence-tagged sites (STSs), which were mapped to the Y

141 g strategy that relies on the development of sequence-tagged sites (STSs).

142 of a series of Y-chromosomal DNA markers, or sequence-tagged sites (STSs).

143 anscript maps use PCR-based landmarks called sequence-tagged sites (STSs).

144 ic EcoRI sites located within or adjacent to sequence-tagged sites (STSs).

145 le-genome-radiation hybrids (WG-RHs) and 271 sequence-tagged sites (STSs).

146 We built the map by screening sequenced-tagged sites (STSs) against a large-insert yea

147 Using existing markers and additional sequence tagged sites, which we have generated, we have

148 These genetically anchored sequence-tagged sites will foster many structural, funct

149 f Dictyostelium discoideum consisting of 300 sequence-tagged sites with an average spacing of 14 kb a