ライフサイエンスコーパス: karyotyping

1 human and mouse with virtual karyotyping (e-karyotyping).

2 number of four was confirmed by cytological karyotyping.

3 n reaction (PCR) method as an alternative to karyotyping.

4 e result was PCR and karyotyping or FISH and karyotyping.

5 re isolated and characterized by chromosomal karyotyping.

6 mparative genomic hybridization and spectral karyotyping.

7 5 early-passage mouse cell lines by spectral karyotyping.

8 on fragment length polymorphism analysis and karyotyping.

9 n fragment length polymorphism analysis, and karyotyping.

10 etitive element 2 probe, and electrophoretic karyotyping.

11 of human (and mouse) chromosomes, i.e. color karyotyping.

12 abnormalities that are detectable by routine karyotyping.

13 urther analysed for chromosomal stability by karyotyping.

14 human cells in the cultures was confirmed by karyotyping.

15 th no translocation detected by conventional karyotyping.

16 ges through senescence, gene expression, and karyotyping.

17 are intractable, or cryptic, to both CMA and karyotyping.

18 ntent in four Afrotherian species using flow karyotyping.

19 ping libraries when used to augment prenatal karyotyping.

20 ping, RNA expression profiling, and spectral karyotyping.

21 -based comparative genomic hybridization and karyotyping.

22 and their genomic integrity was confirmed by karyotyping.

23 .4%; 95% CI, 37%-44%): 26 of 59 (44.1%) with karyotyping, 32 of 188 (17.0%) with microarrays, 31 of 1

24 rom six cell lines were analyzed by spectral karyotyping, a technique that allows one to visualize al

25 Whole-genome scanning by spectral karyotyping allowed instantaneous visualization of defin

26 of these new strain pairs was established by karyotyping, amplified fragment length polymorphism geno

27 with live NSCs (to prevent cell fusion) and karyotyping analyses, revealed that NSCs had differentia

28 hromosomes in the primary tumor and spectral karyotyping analysis of derived cell lines identify chro

29 Spectral karyotyping analysis of metaphase chromosomes from prima

30 ARA in leukemogenesis, we performed spectral karyotyping analysis of myeloid leukemias from hMRP8-PML

31 operate with PML-RARA, we performed spectral karyotyping analysis of myeloid leukemias from transgeni

32 Comparative karyotyping analysis revealed that chromosome organizati

33 chromosomal aberrations as shown by spectral karyotyping analysis, suggesting changes beyond neu sign

34 secondary genetic events, by using spectral karyotyping analysis.

35 mined by metaphase spread assay and spectral karyotyping analysis.

36 or numerical chromosome changes based on SKY karyotyping analysis.

37 d and 3049 chorionic villus samples that had karyotyping and a rapid test on the same sample, none of

38 l abnormalities is typically investigated by karyotyping and array-based detection of microscopically

39 Digital karyotyping and array-based techniques including array c

40 grammes for Down's syndrome need not include karyotyping and can offer prenatal diagnosis for the syn

41 Karyotyping and comparative genomic hybridization identi

42 High-resolution molecular karyotyping and comparative genomics with Setaria italic

43 the rate of aneuploidy observed by spectral karyotyping and detected aneuploidy in adult neurons.

44 ed with these two approaches of quantitative karyotyping and FISH.

45 rearrangements already mapped regionally by karyotyping and fluorescence in situ hybridization, a ta

46 comparative genomic hybridization, spectral karyotyping and fluorescence in situ hybridization, reve

47 ridization, and 3) chromosomal polysomies by karyotyping and fluorescence in situ hybridization.

48 mosome number and identity using traditional karyotyping and fluorescence in situ hybridization.

49 the RECORD libraries may be used for digital karyotyping and for pathogen identification by computati

50 y of all marker chromosomes from our initial karyotyping and G-band analysis.

51 Cells were investigated by karyotyping and gene expression analysis of the CD34(+)

52 d in the cyclin D1-rescued cells by spectral karyotyping and immunofluorescence.

53 Utilizing spectral karyotyping and locus-specific fluorescence in situ hybr

54 Karyotyping and multiplex ligation-dependent probe ampli

55 We performed metaphase karyotyping and next-generation sequencing (NGS) of 85 g

56 single nucleotide polymorphism array (SNP-A) karyotyping and parallel sequencing of 22 genes frequent

57 Molecular methods, including karyotyping and restriction enzyme analysis, confirmed t

58 Spectral karyotyping and short tandem repeat analysis of the UISO

59 The high resolution of digital karyotyping and single nucleotide polymorphism arrays pe

60 We applied digital karyotyping and single nucleotide polymorphism arrays to

61 hese aberrations were originally detected by karyotyping and then by more sophisticated cytogenetic a

62 ant cytogenetic information as compared with karyotyping and was equally efficacious in identifying a

63 the genetic basis of SAMS, we used molecular karyotyping and whole-exome sequencing (WES) to study sm

64 by using MSDK (methylation-specific digital karyotyping) and SAGE (serial analysis of gene expressio

65 d a new method, methylation-specific digital karyotyping, and applied it to epithelial and myoepithel

66 echnologies such as multiplex FISH, spectral karyotyping, and comparative genomic hybridization.

67 ed to antifungal susceptibility testing, DNA karyotyping, and evaluation of the expression of genes p

68 sing additional cytogenetic profile testing, karyotyping, and genetic and protein profiling, we concl

69 of large CLL cohorts, as well as stimulated karyotyping, are discussed.

70 -regulated Hoxb8 protein, demonstrate normal karyotyping, are genetically tractable, and can be diffe

71 h conventional cytogenetics methods, digital karyotyping, array comparative genomic hybridization, an

72 We used a combination of spectral karyotyping, array comparative genomic hybridization, an

73 supports the use of CMA in place of G-banded karyotyping as the first-tier cytogenetic diagnostic tes

74 Here we describe a modification of digital karyotyping-biome representational in silico karyotyping

75 karyotyping-biome representational in silico karyotyping (BRISK)-as a general technique for analyzing

76 ing method (biome representational in silico karyotyping [BRiSK]) were applied in parallel to samples

77 and unbalanced rearrangements identified on karyotyping but did not identify balanced translocations

78 Karyotyping by PFGE appears to be the most useful molecu

79 iation of the cultures were characterized by karyotyping, cell morphology, and growth kinetics studie

80 taphase spreads and to complete a FISH-based karyotyping cocktail that permitted simultaneous identif

81 orescence in situ hybridization (FISH)-based karyotyping cocktail was developed with which to study t

82 SH using the yeast DNA probe together with a karyotyping cocktail.

83 fluorescence in-situ hybridization, spectral karyotyping, comparative genomic hybridization, loss of

84 fluorescence in situ hybridization, spectral karyotyping, cross-species color banding, and comparativ

85 Spectral karyotyping data showed several chromosomal aberrations

86 mples within each class made transcriptional karyotyping difficult without pooling or the use of arra

87 Among comparison isolates, karyotyping distinguished some isolates that were indist

88 ll samples from human and mouse with virtual karyotyping (e-karyotyping).

89 nzyme electrophoresis (MEE), electrophoretic karyotyping (EK), random-amplified polymorphic DNA (RAPD

90 tion of the tick cells was confirmed by PCR, karyotyping, electron microscopy, and reinfection of bov

91 powerful cytogenetic tools such as spectral karyotyping, fluorescence in situ hybridization and comp

92 en assessed by chromosome counting, spectral karyotyping, fluorescence in situ hybridization, and DNA

93 cular genetic analyses, such as conventional karyotyping, fluorescence in situ hybridization, reverse

94 detectable by cytogenetic analysis (standard karyotyping), fluorescent in situ hybridisation (FISH),

95 at 11-14 weeks' gestation immediately before karyotyping for a possible chromosomal abnormality detec

96 romosomal abnormalities (BCAs) still require karyotyping for clinical detection.

97 s; (iii) teratoma formation assays; and (iv) karyotyping for genomic stability.

98 gests that using AGH instead of conventional karyotyping for most ID patients provides good value for

99 mosomal microarray analysis as compared with karyotyping for routine prenatal diagnosis.

100 his method for RNA-Seq data and present eSNP-Karyotyping for the detection of chromosomal aberrations

101 ii f. sp. carinii defined by electrophoretic karyotyping (forms 1 and 2).

102 In addition to the problem of karyotyping, genomic and molecular genetic studies of an

103 ll into five categories, in which multicolor karyotyping has produced erroneous interpretations.

104 .21]; P < .001) and del(17p) by conventional karyotyping (hazard ratio, 7.96 [1.02-61.92]; P = .048)

105 Spectral karyotyping identified multiple chromosomal rearrangemen

106 Combined metaphase and SNP-A karyotyping improved detection of chromosomal lesions: 1

107 demonstrated complexity that was cryptic to karyotyping in 21% of BCAs, highlighting the limitations

108 and deletions in these tumors using digital karyotyping in combination with expression analysis.

109 efelter's syndrome was confirmed by FISH and karyotyping in the fifth.

110 is work demonstrates the utility of FISH and karyotyping in the study of transposon activity and its

111 luorescence in situ hybridization (FISH) and karyotyping in transformed B cell lines.

112 ays against ground truth defined by spectral karyotyping, in addition to comparing the concordance of

113 med by SuperTAG methylation-specific digital karyotyping, in order to identify genes differentially m

114 fic surface markers, isoenzyme analysis, and karyotyping indicate that they are hybrid in nature.

115 last (TIELF) cells by G banding and spectral karyotyping indicated that forced extension of the life

116 fish chromosomes, as previously indicated by karyotyping, indicates that there are no especially gene

117 Metaphase karyotyping is an established diagnostic standard in acu

118 Digital karyotyping is based on counting the sequence tags that

119 identifying chromosomes, a process known as karyotyping, is widely used to detect changes in chromos

120 agnosis at 29 centers were sent to a central karyotyping laboratory.

121 Combined MC/SNP-A karyotyping lead to higher diagnostic yield of chromosom

122 Digital karyotyping libraries can be generated in about a week,

123 In addition, as revealed by spectral karyotyping, LMP1 induced "outre" giant cells and hypopl

124 single-nucleotide polymorphism array (SNP-A) karyotyping may be used to find cryptic abnormalities an

125 e development of an inexpensive and scalable karyotyping method would allow rapid detection and chara

126 ighly sensitive method of Minimally Invasive Karyotyping (MINK) for the diagnosis of the fetal geneti

127 pplicability of Methylation Specific Digital Karyotyping (MSDK), a non-array based method, for the pr

128 veloped method--methylation-specific digital karyotyping (MSDK)--that enables comprehensive and unbia

129 diagnostic yield of genomic tools (molecular karyotyping, multi-gene panel and exome sequencing) in a

130 We demonstrate in vivo karyotyping of chromosomes during mitosis and identify d

131 n (FISH) on somatic chromosomes coupled with karyotyping of each chromosome.

132 were found as robust cytogenetic markers for karyotyping of meadow fescue and ryegrass species and th

133 Through digital karyotyping of permanent medulloblastoma cell lines, we

134 Karyotyping of the cord blood cells from 15 ARV-exposed

135 Karyotyping of the patient and of both parents was norma

136 n 3 of 4 sex-mismatched specimens, tissue XY-karyotyping of the RPM interphase cells was consistent w

137 Performing CMA and G-banded karyotyping on every patient substantially increases the

138 Phenotype was assessed by fetal karyotyping or clinical examination of liveborn infants.

139 tients who had known ploidy status either by karyotyping or DNA content measurement using flow cytome

140 ocol for an interpretable result was PCR and karyotyping or FISH and karyotyping.

141 developed a novel approach, termed spectral karyotyping or SKY based on the hybridization of 24 fluo

142 Digital karyotyping provides a broadly applicable means for syst

143 This amplification was validated by digital karyotyping, quantitative real-time PCR, and dual-color

144 While fluorescence in situ hybridization and karyotyping reveal many abnormalities, SNP chips provide

145 Spectral karyotyping revealed a complex rearrangement disrupting

146 Karyotyping revealed that approximately 33% of mitotic S

147 uorescent in-situ hybridization and spectral karyotyping revealed that nine out of nine lymphomas con

148 Karyotyping revealed the same PFGE pattern for the nine

149 Karyotyping reveals that these tumors frequently harbor

150 Karyotyping showed that development of chromosomal chang

151 f species identity mismatch, electrophoretic karyotyping showed that the RAPD fingerprint was correct

152 petitive element 2 probe and electrophoretic karyotyping showed two distinct banding patterns among p

153 e is not deleted in OGS cell lines, however, karyotyping shows gross abnormalities involving chromoso

154 SNP-A-based karyotyping shows superior resolution for chromosomal de

155 Strikingly, spectral karyotyping (SKY) analysis revealed that loss of telomer

156 isplay cytogenetic abnormalities by spectral karyotyping (SKY) analysis.

157 Spectral karyotyping (SKY) and fluorescent-in-situ hybridization

158 r karyotyping technologies, such as spectral karyotyping (SKY) and multiplex (M-) FISH, have proved t

159 e and metastatic phenotype, we used spectral karyotyping (SKY) in combination with comparative genomi

160 This notion is supported by spectral karyotyping (SKY) of metaphase chromosomes, which displa

161 romosomal analysis using multicolor spectral karyotyping (SKY) revealed that there were multiple chro

162 rring translocations in MM, we used spectral karyotyping (SKY) to analyze a panel of nine bone marrow

163 We have applied spectral karyotyping (SKY) to chemically induced plasmocytomas, m

164 Here we use multicolor spectral karyotyping (SKY) to evaluate 10 established BALB/c plas

165 omosomal aberrations, using CGH and spectral karyotyping (SKY) was performed in our recently establis

166 Multicolor spectral karyotyping (SKY) was performed on bone marrow samples f

167 rative genomic hybridization (CGH), spectral karyotyping (SKY), and fluorescence in situ hybridizatio

168 Spectral karyotyping (SKY), and the related multiplex fluorescenc

169 a cell line HeLa through the use of spectral karyotyping (SKY), comparative genomic hybridization (CG

170 The molecular cytogenetic technique spectral karyotyping (SKY), on the other hand, enables complete c

171 l acute lymphoblastic leukemia with spectral karyotyping (SKY), which can identify all chromosomes si

172 ve genomic hybridization (CGH), and spectral karyotyping (SKY).

173 ement was assembled, allowing a small-target karyotyping system to be developed.

174 ed Mutator element, RescueMu, via use of the karyotyping system.

175 wo putative progenitors using our FISH-based karyotyping system.

176 Using a novel karyotyping technique, we demonstrate that complete disr

177 -chromosome changes and may augment standard karyotyping techniques by providing additional molecular

178 Multicolor karyotyping technologies, such as spectral karyotyping (

179 PCR karyotyping that refined the region on chromosome 6 iden

180 We have developed a method, called digital karyotyping, that provides quantitative analysis of DNA

181 irectly on all cases with negative molecular karyotyping, the diagnostic yield of exome sequencing wa

182 parative genomic hybridization, and spectral karyotyping to a series of nine established cell lines.

183 We have used spectral karyotyping to assess potential roles of three different

184 We applied high-density SNP-A karyotyping to identify loss of heterozygosity of 11q in

185 classical cytogenetic analysis and spectral karyotyping to investigate the chromosomal segregation d

186 ion in XLP patient 43-004 by dual-laser flow karyotyping to involve 2% of the X chromosome, or approx

187 y for the transition from traditional fungal karyotyping to more comprehensive chromosome biology stu

188 We used spectral karyotyping to provide a detailed analysis of karyotypic

189 (LOH) of chromosome 1 has been suggested, by karyotyping, to be an initial episode in human hepatocar

190 e recently been widely applied as a powerful karyotyping tool in numerous translational cancer studie

191 We applied these karyotyping tools to wild soybean, G. soja Sieb. and Zuc

192 Digital karyotyping uses short sequence tags derived from specif

193 XY-karyotyping using fluorescence in situ hybridization was

194 In search of a related mechanism, spectral karyotyping was carried out, showing premature chromatid

195 Each sample was split in two; standard karyotyping was performed on one portion and the other w

196 In this study, digital karyotyping was used to search for genomic alterations i

197 A genomewide technology, digital karyotyping, was used to identify subchromosomal alterat

198 rescence in situ hybridization, and spectral karyotyping, we identified structural aberrations and co

199 Chromosomal aberrations as assessed by karyotyping were observed in 68.8% of 154 patients, 31.2

200 e genomic hybridization (aCGH) and metaphase karyotyping were performed.

201 single nucleotide polymorphism array (SNP-A) karyotyping were used to assess the relative contributio

202 mal truncation came from the results of FISH karyotyping, which revealed broken chromosomes with tran

203 New technologies such as a spectral karyotyping will likely increase out ability to identify

204 Replacement of full karyotyping with rapid testing for trisomies 13, 18, and

205 ytogenetic testing comparing CMA to G-banded karyotyping with respect to technical advantages and lim

206 istent by phenotyping and by electrophoretic karyotyping with the European reference strain of C. dub

207 les, rapid aneuploidy testing replacement of karyotyping would have resulted in about one in 100 and