| 11q_FISH |
11q gain/loss by FISH |
| 1p19q |
1p/19q codeletion |
| ALKtFISH |
ALK(2p23) translocation by FISH |
| API2MALTtFISH |
API2/MALT1 (11;18) (q21;q21) translocation by FISH |
| ATMdelFISH |
ATM (11q22.3) deletion by FISH |
| BCL2tFISH |
BCL2 (18q21)translocation by FISH |
| BCL6tFISH |
BCL6 (3q27) translocation by FISH |
| BRAFmut |
BRAF V600 mutation by RT-PCR |
| CCND1tFISH |
CCND1 translocation by FISH |
| DDIT3FISH |
DDIT3 breakapart FISH |
| DNR |
|
| EBERCISH |
EBER (EBSTEIN BAR virus) by CISH |
| EGFRmut |
EGFR mutacions in exons 18-21 by RT-PCR |
| EGFRmutKiti |
EGFR mutacions in exons 18-21 by RT-PCR |
| EGFRmutPlazma |
EGFR iÅ plazmos |
| EWINGtFISH |
EWING (11;22)(q24;q12) translocation by FISH |
| FOXO1FISH |
FOXO1 breakapart FISH |
| HEmol |
|
| HemolProsigna |
|
| HEmolpulmo |
|
| HER2ampFISH |
HER2 (17q12) amplification by FISH |
| HPV |
HPV by PGR |
| HPV_GK1 |
HPV by PGR |
| HPV_GK3 |
HPV by PGR |
| HPV_GK4 |
HPV by PGR |
| HPVa |
HPV by PGR |
| HPVakc |
HPV by PGR |
| HPVVLK |
HPV by PGR |
| HPVVLK12 |
HPV by PGR |
| IgHMYCtFISH |
IGH/MYC (8;14)(q24;q32) translocation by FISH |
| IRF4/DUSP22(6p25.3) |
IRF4/DUSP22 (6p25.3) break translocation by FISH |
| YWHAE(17p13.3) |
YWHAE (17p13.3) break translocation by FISH |
| JAZF1(7p15.1-p15.2) |
JAZF1 (7p15.1-p15.2) break translocation by FISH |
| KRASmut |
KRAS mutations in codons 12,13 and 61 by RT-PCR |
| LPI |
STI by PGR |
| LPI_GK1 |
STI by PGR |
| LPI_GK2 |
STI by PGR |
| LPI_GK3 |
STI by PGR |
| MAML2FISH |
MAML2 breakapart FISH |
| MDM2FISH |
MDM2/CEN 12 amplification |
| MYCtFISH |
MYC (8q24) translocation by FISH |
| MSImut |
Mikrosatelitų nestabilumo tyrimas RL-PGR metodu |
| N-MYCampFISH |
N-MYC (2p24) amplification by FISH |
| NRASmut |
Detection of somatic mutations in and near NRAS codons 12-13, 59-61, 117 and 146 in a nucleic acid extract from FFPE material |
| PDGFBFISH |
PDGFB breakapart FISH |
| PloidyFISH |
|
| SYTFISH |
SS18 breakapart FISH |
| TFE3tFISH |
TFE3 (Xp11.23)translocation by FISH |
| USP6FISH |
USP6 Dual Color Break Apart Probe to detect translocations involving the chromosomal region 17p13.2 harboring the USP6 gene |