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Σε αυτήν τη σελίδα μπορείτε να λάβετε μια λεπτομερή ανάλυση μιας λέξης ή μιας φράσης, η οποία δημιουργήθηκε χρησιμοποιώντας το ChatGPT, την καλύτερη τεχνολογία τεχνητής νοημοσύνης μέχρι σήμερα:
- πώς χρησιμοποιείται η λέξη
- συχνότητα χρήσης
- χρησιμοποιείται πιο συχνά στον προφορικό ή γραπτό λόγο
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- παραδείγματα χρήσης (πολλές φράσεις με μετάφραση)
- ετυμολογία
Τι (ποιος) είναι genomic imprinting - ορισμός
Genomic imprinting
PHENOMENON THAT CAUSES GENES TO BE EXPRESSED IN A PARENT-OF-ORIGIN-SPECIFIC MANNER
Epigenetic imprinting; Genetic imprint; Genetic imprinting; Parental imprinting; Imprinting human; Imprinting (genetics); Genomic Imprinting; Imprinted genes; Imprinted gene; Kinship theory of genomic imprinting; Gametic imprinting; Gene imprinting; Imprinting control region; The kinship theory of genomic imprinting; Imprinting disorder; Imprinted loci; Paternally imprinted genes
Genomic imprinting is an epigenetic phenomenon that causes genes to be expressed or not, depending on whether they are inherited from the mother or the father. Genes can also be partially imprinted.
Genomic island
PART OF A GENOME THAT HAS EVIDENCE OF HORIZONTAL ORIGINS
Genomic islands; Genetic island
A genomic island (GI) is part of a genome that has evidence of horizontal origins. The term is usually used in microbiology, especially with regard to bacteria.
Comparative genomic hybridization
METHOD TO EVALUATE BIOLOGICAL SAMPLES
Comparative genomic hybridization (CGH); Array-comparative genomic hybridization; ACGH; Array CGH; Comparative Genomic Hybridization; Comparative Genomic Hybridisation; Comparative hybridization; Array comparative genomic hybridisation; Cot 1 DNA; Cot-1 DNA; Comparative genome hybridization; Chromosomal microarray analysis; CGH array; Array comparative genomic hybridization; Array-comparative Genomic Hybridization; Microarray-based comparative genomic hybridization; A-CGH; Array hybridization
Comparative genomic hybridization (CGH) is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared to a reference sample, without the need for culturing cells. The aim of this technique is to quickly and efficiently compare two genomic DNA samples arising from two sources, which are most often closely related, because it is suspected that they contain differences in terms of either gains or losses of either whole chromosomes or subchromosomal regions (a portion of a whole chromosome).
