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1 of each duplication were determined by array comparative genome hybridization.
2 ber in solid tumors by cDNA microarray-based comparative genome hybridization.
3 ied on the basis of read-depth variation and comparative genome hybridization.
4 cross the genome was analyzed by array-based comparative genome hybridization.
5 was evaluated using four sets of microarray comparative genome hybridization (aCGH) data, which incl
6 use genome-wide oligonucleotide-based array comparative genome hybridization (aCGH) followed by rapi
7 n of next-generation sequencing (NGS), array-Comparative Genome Hybridization (aCGH) screening, famil
9 following shRNA treatment, was confirmed by Comparative Genome Hybridization analyses of the same DN
12 Using forward genetic methods combined with comparative genome hybridization analysis, we were able
14 ence factors whose function was supported by comparative genome hybridization and expression profilin
15 nd optimized the probe set using solid phase comparative genome hybridization and liquid phase exome
16 ome), polymorphism discovery and genotyping, comparative genome hybridization, and genome resequencin
22 ially developed to analyse data derived from comparative genome hybridization (CGH) microarray experi
29 haracteristics and data from high-resolution comparative genome hybridization experiments in a discre
30 ome (69.2%) and plasmid (66%), together with comparative genome hybridization experiments, suggest th
31 ping, fluorescence in situ hybridization and comparative genome hybridization have improved our abili
34 ons have been experimentally validated using comparative genome hybridization on tiling-resolution ol
35 at permits high-resolution genome-wide array-comparative genome hybridization profiling of human and
36 ts were recovered at very low frequency, and comparative genome hybridizations revealed that Deltalmx
37 and (iii) genes identified by clinical array comparative genome hybridization studies as potentially
39 lied multiplex polymerase chain reaction and comparative genome hybridization to identify potential v
40 quence variation (re-sequencing, genotyping, comparative genome hybridization), transcription (expres
42 chaffeensis strains Wakulla and Liberty, and comparative genome hybridization was performed using a d
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