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1 human and mouse with virtual karyotyping (e-karyotyping).
2 and their genomic integrity was confirmed by karyotyping.
3 number of four was confirmed by cytological karyotyping.
4 n reaction (PCR) method as an alternative to karyotyping.
5 e result was PCR and karyotyping or FISH and karyotyping.
6 re isolated and characterized by chromosomal karyotyping.
7 mparative genomic hybridization and spectral karyotyping.
8 5 early-passage mouse cell lines by spectral karyotyping.
9 on fragment length polymorphism analysis and karyotyping.
10 n fragment length polymorphism analysis, and karyotyping.
11 etitive element 2 probe, and electrophoretic karyotyping.
12 of human (and mouse) chromosomes, i.e. color karyotyping.
13 abnormalities that are detectable by routine karyotyping.
14 urther analysed for chromosomal stability by karyotyping.
15 human cells in the cultures was confirmed by karyotyping.
16 th no translocation detected by conventional karyotyping.
17 mosaic, or translocation) confirmed through karyotyping.
18 tility of OMKar for OGM-based constitutional karyotyping.
19 ges through senescence, gene expression, and karyotyping.
20 are intractable, or cryptic, to both CMA and karyotyping.
21 ntent in four Afrotherian species using flow karyotyping.
22 ping libraries when used to augment prenatal karyotyping.
23 ping, RNA expression profiling, and spectral karyotyping.
24 -based comparative genomic hybridization and karyotyping.
25 .4%; 95% CI, 37%-44%): 26 of 59 (44.1%) with karyotyping, 32 of 188 (17.0%) with microarrays, 31 of 1
26 rom six cell lines were analyzed by spectral karyotyping, a technique that allows one to visualize al
28 of these new strain pairs was established by karyotyping, amplified fragment length polymorphism geno
29 with live NSCs (to prevent cell fusion) and karyotyping analyses, revealed that NSCs had differentia
30 hromosomes in the primary tumor and spectral karyotyping analysis of derived cell lines identify chro
32 ARA in leukemogenesis, we performed spectral karyotyping analysis of myeloid leukemias from hMRP8-PML
33 operate with PML-RARA, we performed spectral karyotyping analysis of myeloid leukemias from transgeni
35 o transfer cycles of 692 women who underwent karyotyping analysis using Giemsa-Trypsin-Leishman (GTL)
37 chromosomal aberrations as shown by spectral karyotyping analysis, suggesting changes beyond neu sign
41 d and 3049 chorionic villus samples that had karyotyping and a rapid test on the same sample, none of
42 -pair, and linked-read sequencing as well as karyotyping and array CGH analysis to identify a wide sp
43 l abnormalities is typically investigated by karyotyping and array-based detection of microscopically
45 grammes for Down's syndrome need not include karyotyping and can offer prenatal diagnosis for the syn
48 the rate of aneuploidy observed by spectral karyotyping and detected aneuploidy in adult neurons.
50 rearrangements already mapped regionally by karyotyping and fluorescence in situ hybridization, a ta
51 comparative genomic hybridization, spectral karyotyping and fluorescence in situ hybridization, reve
54 the RECORD libraries may be used for digital karyotyping and for pathogen identification by computati
61 single nucleotide polymorphism array (SNP-A) karyotyping and parallel sequencing of 22 genes frequent
66 pothesis, we designed a molecular marker for karyotyping and studied natural and experimental populat
67 hese aberrations were originally detected by karyotyping and then by more sophisticated cytogenetic a
68 ant cytogenetic information as compared with karyotyping and was equally efficacious in identifying a
69 the genetic basis of SAMS, we used molecular karyotyping and whole-exome sequencing (WES) to study sm
70 by using MSDK (methylation-specific digital karyotyping) and SAGE (serial analysis of gene expressio
71 d a new method, methylation-specific digital karyotyping, and applied it to epithelial and myoepithel
73 ed to antifungal susceptibility testing, DNA karyotyping, and evaluation of the expression of genes p
74 sing additional cytogenetic profile testing, karyotyping, and genetic and protein profiling, we concl
76 -regulated Hoxb8 protein, demonstrate normal karyotyping, are genetically tractable, and can be diffe
77 h conventional cytogenetics methods, digital karyotyping, array comparative genomic hybridization, an
79 supports the use of CMA in place of G-banded karyotyping as the first-tier cytogenetic diagnostic tes
80 uction, whole-genome sequencing and spectral karyotyping-based single-cell phylogenetic tree building
81 Here we describe a modification of digital karyotyping-biome representational in silico karyotyping
83 itative 16S rDNA PCR, biome representational karyotyping (BRiSK), and quantitative PCR (qPCR) confirm
84 karyotyping-biome representational in silico karyotyping (BRISK)-as a general technique for analyzing
85 ing method (biome representational in silico karyotyping [BRiSK]) were applied in parallel to samples
86 and unbalanced rearrangements identified on karyotyping but did not identify balanced translocations
88 iation of the cultures were characterized by karyotyping, cell morphology, and growth kinetics studie
89 6) had received former diagnostic results by karyotyping characteristic of normal human male or femal
90 asis of NTDs remains poorly understood using karyotyping, chromosomal microarray, and short-read sequ
91 taphase spreads and to complete a FISH-based karyotyping cocktail that permitted simultaneous identif
92 orescence in situ hybridization (FISH)-based karyotyping cocktail was developed with which to study t
94 fluorescence in-situ hybridization, spectral karyotyping, comparative genomic hybridization, loss of
95 fluorescence in situ hybridization, spectral karyotyping, cross-species color banding, and comparativ
97 mples within each class made transcriptional karyotyping difficult without pooling or the use of arra
100 nzyme electrophoresis (MEE), electrophoretic karyotyping (EK), random-amplified polymorphic DNA (RAPD
101 tion of the tick cells was confirmed by PCR, karyotyping, electron microscopy, and reinfection of bov
102 powerful cytogenetic tools such as spectral karyotyping, fluorescence in situ hybridization and comp
103 en assessed by chromosome counting, spectral karyotyping, fluorescence in situ hybridization, and DNA
104 cular genetic analyses, such as conventional karyotyping, fluorescence in situ hybridization, reverse
105 detectable by cytogenetic analysis (standard karyotyping), fluorescent in situ hybridisation (FISH),
106 at 11-14 weeks' gestation immediately before karyotyping for a possible chromosomal abnormality detec
109 gests that using AGH instead of conventional karyotyping for most ID patients provides good value for
111 his method for RNA-Seq data and present eSNP-Karyotyping for the detection of chromosomal aberrations
114 ll into five categories, in which multicolor karyotyping has produced erroneous interpretations.
115 .21]; P < .001) and del(17p) by conventional karyotyping (hazard ratio, 7.96 [1.02-61.92]; P = .048)
119 demonstrated complexity that was cryptic to karyotyping in 21% of BCAs, highlighting the limitations
120 and deletions in these tumors using digital karyotyping in combination with expression analysis.
122 is work demonstrates the utility of FISH and karyotyping in the study of transposon activity and its
124 ays against ground truth defined by spectral karyotyping, in addition to comparing the concordance of
125 med by SuperTAG methylation-specific digital karyotyping, in order to identify genes differentially m
126 fic surface markers, isoenzyme analysis, and karyotyping indicate that they are hybrid in nature.
127 last (TIELF) cells by G banding and spectral karyotyping indicated that forced extension of the life
128 fish chromosomes, as previously indicated by karyotyping, indicates that there are no especially gene
129 s of this study support the incorporation of karyotyping into the standard diagnostic workup of CLL,
132 collected on lymphoid malignancies, because karyotyping is part of the standard of care in these can
133 identifying chromosomes, a process known as karyotyping, is widely used to detect changes in chromos
138 single-nucleotide polymorphism array (SNP-A) karyotyping may be used to find cryptic abnormalities an
139 e development of an inexpensive and scalable karyotyping method would allow rapid detection and chara
140 ighly sensitive method of Minimally Invasive Karyotyping (MINK) for the diagnosis of the fetal geneti
141 pplicability of Methylation Specific Digital Karyotyping (MSDK), a non-array based method, for the pr
142 veloped method--methylation-specific digital karyotyping (MSDK)--that enables comprehensive and unbia
143 diagnostic yield of genomic tools (molecular karyotyping, multi-gene panel and exome sequencing) in a
145 ian segmentation approach called copy number karyotyping of aneuploid tumors (CopyKAT) to estimate ge
148 were found as robust cytogenetic markers for karyotyping of meadow fescue and ryegrass species and th
152 n 3 of 4 sex-mismatched specimens, tissue XY-karyotyping of the RPM interphase cells was consistent w
155 tients who had known ploidy status either by karyotyping or DNA content measurement using flow cytome
157 developed a novel approach, termed spectral karyotyping or SKY based on the hybridization of 24 fluo
159 This amplification was validated by digital karyotyping, quantitative real-time PCR, and dual-color
160 While fluorescence in situ hybridization and karyotyping reveal many abnormalities, SNP chips provide
163 uorescent in-situ hybridization and spectral karyotyping revealed that nine out of nine lymphomas con
167 f species identity mismatch, electrophoretic karyotyping showed that the RAPD fingerprint was correct
168 petitive element 2 probe and electrophoretic karyotyping showed two distinct banding patterns among p
169 e is not deleted in OGS cell lines, however, karyotyping shows gross abnormalities involving chromoso
174 r karyotyping technologies, such as spectral karyotyping (SKY) and multiplex (M-) FISH, have proved t
175 e and metastatic phenotype, we used spectral karyotyping (SKY) in combination with comparative genomi
177 romosomal analysis using multicolor spectral karyotyping (SKY) revealed that there were multiple chro
178 rring translocations in MM, we used spectral karyotyping (SKY) to analyze a panel of nine bone marrow
181 omosomal aberrations, using CGH and spectral karyotyping (SKY) was performed in our recently establis
183 rative genomic hybridization (CGH), spectral karyotyping (SKY), and fluorescence in situ hybridizatio
186 a cell line HeLa through the use of spectral karyotyping (SKY), comparative genomic hybridization (CG
187 The molecular cytogenetic technique spectral karyotyping (SKY), on the other hand, enables complete c
188 l acute lymphoblastic leukemia with spectral karyotyping (SKY), which can identify all chromosomes si
195 -chromosome changes and may augment standard karyotyping techniques by providing additional molecular
198 We have developed a method, called digital karyotyping, that provides quantitative analysis of DNA
199 irectly on all cases with negative molecular karyotyping, the diagnostic yield of exome sequencing wa
200 parative genomic hybridization, and spectral karyotyping to a series of nine established cell lines.
203 classical cytogenetic analysis and spectral karyotyping to investigate the chromosomal segregation d
204 ion in XLP patient 43-004 by dual-laser flow karyotyping to involve 2% of the X chromosome, or approx
205 y for the transition from traditional fungal karyotyping to more comprehensive chromosome biology stu
207 (LOH) of chromosome 1 has been suggested, by karyotyping, to be an initial episode in human hepatocar
208 e recently been widely applied as a powerful karyotyping tool in numerous translational cancer studie
212 In search of a related mechanism, spectral karyotyping was carried out, showing premature chromatid
216 rescence in situ hybridization, and spectral karyotyping, we identified structural aberrations and co
219 single nucleotide polymorphism array (SNP-A) karyotyping were used to assess the relative contributio
220 mal truncation came from the results of FISH karyotyping, which revealed broken chromosomes with tran
223 ytogenetic testing comparing CMA to G-banded karyotyping with respect to technical advantages and lim
224 istent by phenotyping and by electrophoretic karyotyping with the European reference strain of C. dub
225 les, rapid aneuploidy testing replacement of karyotyping would have resulted in about one in 100 and