MIKULÁŠOVÁ, Aneta, Jan SMETANA, Markéta WAYHELOVÁ, Helena JANYŠKOVÁ, Samuel Adeyinka OKUBOTE, Roman HÁJEK a Petr KUGLÍK. Whole genome amplification effect on segmental copy-number changes and copy-number neutral loss of heterozygosity analysis by oligonucleotide-array based comparative genomic hybridization in human myeloma cell line. International Journal of Clinical and Experimental Pathology. 2016, roč. 9, č. 7, s. 6965-6980. ISSN 1936-2625.
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Základní údaje
Originální název Whole genome amplification effect on segmental copy-number changes and copy-number neutral loss of heterozygosity analysis by oligonucleotide-array based comparative genomic hybridization in human myeloma cell line
Autoři MIKULÁŠOVÁ, Aneta (203 Česká republika, domácí), Jan SMETANA (203 Česká republika, domácí), Markéta WAYHELOVÁ (203 Česká republika, domácí), Helena JANYŠKOVÁ (203 Česká republika, domácí), Samuel Adeyinka OKUBOTE (566 Nigérie, domácí), Roman HÁJEK (203 Česká republika) a Petr KUGLÍK (203 Česká republika, garant, domácí).
Vydání International Journal of Clinical and Experimental Pathology, 2016, 1936-2625.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor Genetika a molekulární biologie
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.706
Kód RIV RIV/00216224:14310/16:00088952
Organizační jednotka Přírodovědecká fakulta
UT WoS 000381729200036
Klíčová slova anglicky whole genome amplification; array-comparative genomic hybridization; copy-number changes
Štítky AKR, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Andrea Mikešková, učo 137293. Změněno: 26. 4. 2017 23:13.
Anotace
Whole genome amplification (WGA) is an approach designed to overcome small amounts of DNA for genome-wide genetic tests used in many clinical applications. Various strategies of WGA have been developed; however, none of them can guarantee the absence of amplification bias. In this study, a total of 4 multiple displacement amplification (MDA)-based and 2 PCR-based WGA kits were compared in their effect on segmental copy-number (CN) changes and copy-number neutral loss of heterozygosity (cnnLOH) detection by 3 microarray platforms: CGH/4×44 K (Agilent), CGH+SNP/4×180 K (Agilent) and CGH+SNP/4×180 K (OGT). Genomic imbalances-rich myeloma cell line U266 was used as material. The main outcomes are as follows: 1) MDA-based WGAs showed higher tendency to generate false positive imbalances in contrast to PCR-based WGAs with higher risk of false negativity; 2) the specific risk of false positivity and/or negativity increased with decreasing CN segments size; 3) single-cell WGAs showed significantly worse effect on results in comparison to WGAs with nanogram level of DNA as input; 4) PCR-based WGAs were incompatible with cnnLOH analysis based on SNP in restriction digestion sites and also showed higher risk of cnnLOH false negativity when combined with analysis based on simple hybridization. In conclusion, the results of this study help to choose WGA according to individual user requirements and options. Moreover, we have shown a strategy to verify and validate segmental CN changes detection by DNA array protocol including any WGA for any purpose to attain the highest efficiency without an unnecessary WGA bias.
Návaznosti
NT13492, projekt VaVNázev: Úloha genetických abnormalit ve vývoji a progresi prekancerózy monoklonální gamapatie nejasného významu
VytisknoutZobrazeno: 24. 4. 2024 15:04