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CancerScreen Panels
Highly optimized NGS panel for somatic cancer
The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >Hybridization-based target enrichment panel with our intrinsic probe design, rebalancing, and molecular barcode technologies to efficiently analyze not only hard-to-capture areas but also challenging samples, such as damaged DNA or RNA.
View Detail >End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
View Detail >Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis !
Celemics offers easy-to-use kit with all components needed from RNA fragmentation to double-stranded cDNA synthesis suitable for NGS.
View Detail >Celemics exclusive enzymes and buffers for enhanced hybridization to ensure improved coverage and uniformity.
View Detail >Proven market-leading purification and size selection efficiency supported by Celemics’ unique magnetic bead-based chemistry. Compatible with all Celemics’ panels as well as other NGS providers
View Detail >High-quality streptavidin bead that selectively isolates biotinylated ligands bound to hybridization probes; minimizing DNA loss during the target enrichment process.
View Detail >CeleNM™ Bead streamlines library quantification and normalization in Next-Generation Sequencing (NGS). Say goodbye to traditional QC processes, saving time and costs while ensuring robust results. Experience uniform sequencing data distribution and comparable on-target ratios with CeleNM™ Bead.
View Detail >Celemics’ highly optimized polymerase ensures market-leading amplification efficiency and accuracy with minimized PCR bias and error rate.
View Detail >Highly optimized library preparation kit to be used with all Celemics ready-to-use or customized panels. Experience the incomparable efficiency and performance for NGS library preparation
View Detail >The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Celemics’ comprehensive NGS panel for somatic cancer allows highly accurate and comprehensive analysis for identifying significant mutations and variants for solid tumors.
Celemics has developed NGS ctDNA-based kits for colon, breast, and lung cancer assays. We have integrated our market-leading proprietary technologies and thoroughly validated and optimized as ready-to-use panels for clinical diagnostics.
Celemics offers end-to-end NGS-based detection and discovery solutions for Biopharma, CRO, and Drug discovery research fields.
In order to overcome the limitations of analyzing clinical diseases with conventional whole exome sequencing, Celemics introduces NGS-based clinical diagnostic solution for efficient detection of disease-causing variants for inherited diseases.
Celemics offers flexible choice of assessing extensive target regions associated with Pharmacogenomics for client-specific drug prescription and drug metabolism.
Celemics’ virus panels are designed to detect and identify disease-causing viruses. With our exclusive technologies, we provide efficient and accurate detection of targeted virus trains as well as procurement of credible data for whole viral genome sequencing.
To fulfill the expectations and growing needs for sequencing animals and plants, Celemics offers range of ready-to-use applicable to agrigenomics field as well as an option for developing customized NGS panel to specifically fit individual research purposes.
With Celemics’ proprietary technologies for assay development and optimization, we offer complete and robust NGS solutions for transcriptome, fusion, and isoform analyses for various sample types and conditions.
Celemics provides comprehensive solution for DNA methylation sequencing with proprietary probes specifically designed for methyl-seq, enabling accurate detection of methylation sites.
Complete solution with flexible panel design for characterization and differentiation of a myriad of microbial species.
Accurate and efficient analysis of IGH population that can detect MRD as low as 10-6 with optimized primers that can minimize sequencing loss and PCR duplications.
Celemics introduces revolutionary BI solution aiming to provide client-specific service. We provide fast, accurate, and sophisticated analyses of your NGS data accompanied by our proprietary bioinformatics pipeline.
The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >End-to-end customized target enrichment panel with assay optimization, validation and even complete BI support. Over 1,000 custom panels developed world-wide. White-labeled customized product for business expansion also available.
View Detail >Utilizing NGS-based target enrichment methods for higher genotyping efficiency and accuracy. Providing cost-effective and optimized experiment compared to conventional methods, such as GBS, PCR and microarray in plant and animal research
View Detail >
Revolutionary Bioinformatics solution providing fast and
accurate, client-specific analysis services.
Trust CAS with your BI analysis
Providing NGS-based diagnostics solutions for biopharma companies. Celemics can develop and deliver a flexible customization and commercialization services while maintaining the market-leading performance for our clients interested in clinical and companion diagnostics.
View Detail >Tailored-fit customized assay development from designing to validation run; including not only the custom panel design but also species-specific or sequencer-specific blockers, followed by reagent conditioning to optimize the individual experiment and sequencer.
View Detail >The most comprehensive whole exome panel that covers the target regions of all major WES panels in the market. With our proprietary technologies, we provide industry-leading performance and efficiency with complete BI solution.
View Detail >Find useful information, insights and tools for your Celemics’ products and services
View Detail >Explore the most up-to-date publications featuring Celemics’ products and services
View Detail >Sharing interesting stories about the world of NGS and how Celemics delivers the innovative NGS solutions to the world of science.
View Detail >Explore a diverse range of engaging video content, from fascinating experiments showcasing cutting-edge research to heartfelt customer testimonials.
View Detail >Find useful information, insights and tools for your Celemics’ products and services
View Detail >In-silico designed and wet-lab validated exclusive probes to ensure state-of-the-art capture performance
View Detail >Stay up-to-date with the latest updates on our activities, events and achievements
View Detail >Let’s change the NGS market together – our global presence and partners world-wide
View Detail >Waiting for your experience with Celemics, an innovative leader in NGS industry
View Detail >Highly optimized NGS panel for somatic cancer
CancerScreen 패널은 Somatic Cancer와 연관 있는 것으로 알려진 765개의 유전자에 속한 유전 변이들을 검출하기 위한 패널입니다. 암종과 연관 있는 유전자들의 유전변이를 정확하게 분석하기 위해 높은 특이도와 민감도를 갖도록 개발된 패널로 비용 효율적인 분석이 가능합니다.
셀레믹스에서는 BI 분석 서비스를 제공하고 있습니다. 1차 (Primary), 2차 (Secondary), 3차 (Tertiary)의 세분화된 수준의 분석 결과를 제공할 수 있어 고객이 원하는 결과의 수준에 따라 다른 분석 결과를 제공하고 있습니다. BI에 익숙하지 않은 고객들도 별도의 세팅 없이 유전 변이 분석 결과를 얻을 수 있습니다.
본 패널은 최대 765개의 고형암 연관 유전자를 포함하며 RefSeq 데이터베이스에 기록된 전체 CDS 영역을 타겟 영역으로 합니다. SNV, InDel, Large InDel, CNV, Gene Rearrangements 및 MSI, TMB를 비롯해 TERT Promoter 영역의 유전 변이까지 모든 종류의 유전 변이를 한 번의 검사로 분석할 수 있습니다.
CancerScreen 패널은 매우 높은 시퀀싱 depth를 바탕으로 낮은 빈도로 발생하나 암종에 중요하다고 알려진 유전 변이들을 정확히 검출할 수 있도록 디자인되었습니다. 독자적인 프로브 디자인 기술을 바탕으로 GC-rich 영역이나 Homologous 영역에 발생하는 유전 변이뿐만 아니라 FFPE, ctDNA와 같은 손상되거나 미량인 샘플에 대해서도 최상의 민감도와 특이도로 중요한 유전변이들을 놓치지 않고 분석할 수 있습니다.
셀레믹스는 모든 NGS 패널에 대해 시약 및 프로토콜 최적화를 진행합니다. 최고의 On-target Ratio, Uniformity를 바탕으로 높은 비용 절감 효과를 누릴 수 있습니다. 더불어 독자적인 시약 개발 기술을 바탕으로 다양한 시퀀싱 플랫폼에 최적화된 NGS 패널을 제공해 드리고 있습니다.
Gene count* | 13/54/99/407/765 genes |
---|---|
Target size | 61/197/299/1,123/2,521 kb + Rearrangement |
Mutation type | SNV, Indel, CNV, Rearrangement, MSI, TMB |
Sample type(amount) | FFPE, frozen tissue, cfDNA, RNA |
Platform | All sequencers from Illumina, Thermo Fisher, MGI, PacBio, and Oxford Nanopore |
Bioinformatics Support | ① Primary Analysis: FASTQ to annotated VCF ② Secondary Analysis: CNV, Large InDel ③ Tertiary Analysis: Clinical interpretation |
ALK | APC | BRAF | EGFR | ERBB2 | KRAS | MET | NRAS | PIK3CA | RET | ROS1 | SMAD4 | TP53 |
ABL1 | AKT1 | ALK | APC | ATM | BRAF | BRCA1 | BRCA2 | CDH1 | CDK4 | CDK6 | CDKN2A |
CSF1R | CTNNB1 | DDR2 | EGFR | ERBB2 | ERBB4 | ESR1 | FGFR1 | FGFR2 | FGFR3 | GNA11 | GNAQ |
GNAS | HRAS | IDH1 | IDH2 | JAK2 | KDR | KIT | KRAS | MAP2K1 | MET | MLH1 | MTOR |
MYC | MYCN | NOTCH1 | NRAS | NTRK1 | PDGFRA | PIK3CA | PTCH1 | PTEN | PTPN11 | RB1 | RET |
ROS1 | SMAD4 | SMO | SRC | STK11 | TP53 |
ABL1 | AKT1 | AKT2 | AKT3 | ALK | APC | ARID1A | ARID1B | ARID2 | ATM | ATRX | AURKA |
AURKB | BARD1 | BCL2 | BLM | BMPR1A | BRAF | BRCA1 | BRCA2 | BRIP1 | CDH1 | CDK4 | CDK6 |
CDKN2A | CHEK2 | CSF1R | CTNNB1 | DDR2 | EGFR | EPCAM | EPHB4 | ERBB2 | ERBB3 | ERBB4 | EZH2 |
FBXW7 | FGFR1 | FGFR2 | FGFR3 | FLT3 | GNA11 | GNAQ | GNAS | HNF1A | HRAS | IDH1 | IDH2 |
IGF1R | ITK | JAK1 | JAK2 | JAK3 | KDR | KIT | KRAS | MDM2 | MET | MLH1 | MPL |
MRE11 | MSH2 | MSH6 | MTOR | MUTYH | NBN | NF1 | NOTCH1 | NPM1 | NRAS | NTRK1 | PALB2 |
PDGFRA | PDGFRB | PIK3CA | PIK3R1 | PMS2 | PRSS1 | PTCH1 | PTCH2 | PTEN | PTPN11 | RAD50 | RAD51C |
RAD51D | RB1 | RET | ROS1 | SLX4 | SMAD4 | SMARCB1 | SMO | SRC | STK11 | SYK | TERT |
TOP1 | TP53 | VHL |
ABL1 | ABL2 | ADGRA2 | AKT1 | AKT2 | AKT3 | ALK | AMER1 | APC | APCDD1 | APEX1 | APOB |
APOBEC1 | AR | ARAF | ARFRP1 | ARID1A | ARID1B | ARID2 | ASXL1 | ATM | ATP11B | ATR | ATRX |
AURKA | AURKB | AXIN1 | AXL | B2M | B3GAT1 | BACH1 | BAP1 | BARD1 | BCL2 | BCL6 | BCL9 |
BCOR | BCR | BIRC2 | BIRC3 | BLM | BRAF | BRCA1 | BRCA2 | BRD2 | BRD3 | BRD4 | BRIP1 |
BTG1 | BTK | BTLA | CARD11 | CASP5 | CASP8 | CBFB | CBL | CD274 | CDK12 | CDK4 | CDK6 |
CDK8 | CDKN1A | CDKN1B | CDKN2A | CDKN2B | CDKN2C | CDX2 | CEBPA | CHD1 | CHD2 | CHD4 | CHEK1 |
CHEK2 | CHUK | CIC | CRBN | CREBBP | CRKL | CRLF2 | CSF1R | CSF2 | CSF2RA | CSF2RB | CSNK2A1 |
CTCF | CTLA4 | CTNNA1 | CTNNB1 | CUL3 | CUL4A | CUL4B | CXCL10 | CXCL11 | CXCL9 | CXCR3 | CYLD |
CYP17A1 | DAXX | DCUN1D1 | DDR2 | DICER1 | DIS3 | DNMT1 | DNMT3A | DOCK2 | DOT1L | EGFR | ELMO1 |
EML4 | EMSY | EP300 | EPHA3 | EPHA5 | EPHA6 | EPHA7 | EPHB1 | EPHB4 | EPHB6 | ERBB2 | ERBB3 |
ERBB4 | ERCC1 | ERCC2 | ERG | ERRFI1 | ESR1 | ETV1 | ETV4 | ETV5 | ETV6 | EWSR1 | EYA2 |
EZH2 | FANCA | FANCC | FANCD2 | FANCE | FANCF | FANCG | FANCI | FANCL | FANCM | FAS | FAT1 |
FAT3 | FBXW7 | FGF1 | FGF10 | FGF12 | FGF14 | FGF19 | FGF2 | FGF23 | FGF3 | FGF4 | FGF6 |
FGF7 | FGFR1 | FGFR2 | FGFR3 | FGFR4 | FH | FLCN | FLT1 | FLT3 | FLT4 | FOXA1 | FOXL2 |
FOXO3 | FOXP3 | FRS2 | FUBP1 | GABRA6 | GAS6 | GATA1 | GATA2 | GATA3 | GATA4 | GATA6 | GID4 |
GLI1 | GNA11 | GNA13 | GNAQ | GNAS | GRIN2A | GRM3 | GSK3B | GUCY1A2 | GZMA | GZMB | GZMH |
H3F3A | HGF | HIST1H3B | HNF1A | HOXA3 | HRAS | HSD3B1 | HSP90AA1 | IDH1 | IDH2 | IDO1 | IDO2 |
IFITM1 | IFITM3 | IFNA1 | IFNB1 | IFNG | IGF1 | IGF1R | IGF2 | IGF2R | IKBKE | IKZF1 | IL12A |
IL12B | IL2 | IL23A | IL6 | IL7R | INHBA | INPP4B | INSR | IRF2 | IRF4 | IRS2 | ITGAE |
ITK | JAK1 | JAK2 | JAK3 | JUN | KAT6A | KDM5A | KDM5C | KDM6A | KDR | KEAP1 | KEL |
KIT | KLF4 | KLHL6 | KMT2A | KMT2B | KMT2C | KNSTRN | KRAS | LAG3 | LMO1 | LRP1B | LRP6 |
LTK | LYN | LZTR1 | MAGI2 | MAGOH | MAML1 | MAP2K1 | MAP2K2 | MAP2K4 | MAP3K1 | MAP3K13 | MAPK1 |
MAX | MCL1 | MDM2 | MDM4 | MED12 | MEF2B | MEN1 | MET | MITF | MLH1 | MPL | MRE11 |
MSH2 | MSH6 | MTOR | MUTYH | MYB | MYC | MYCL | MYCN | MYD88 | MYO18A | NCOA3 | NCOR1 |
NF1 | NF2 | NFE2L2 | NFKBIA | NOTCH1 | NOTCH2 | NOTCH3 | NOTCH4 | NPM1 | NRAS | NSD1 | NSD3 |
NTRK1 | NTRK2 | NTRK3 | NUP93 | NUTM1 | PAK3 | PAK5 | PALB2 | PARP1 | PARP2 | PARP3 | PARP4 |
PAX5 | PBRM1 | PDCD1 | PDCD1LG2 | PDGFRA | PDGFRB | PDK1 | PGR | PHF6 | PHLPP2 | PIK3C2B | PIK3C3 |
PIK3CA | PIK3CB | PIK3CG | PIK3R2 | PKHD1 | PLCG1 | PLCG2 | PMS2 | PNP | PNRC1 | POLD1 | POLE |
PPARG | PPP2R1A | PRDM1 | PREX2 | PRF1 | PRKAR1A | PRKCI | PRKDC | PRPF40B | PRSS8 | PTCH1 | PTCH2 |
PTEN | PTK2 | PTPN11 | PTPRC | PTPRD | QKI | RAB35 | RAC1 | RAC2 | RAD17 | RAD50 | RAD51 |
RAD52 | RAD54L | RAF1 | RANBP2 | RARA | RB1 | RBM10 | REL | RET | RHEB | RHOA | RHOB |
RICTOR | ROBO1 | ROBO2 | ROS1 | RPA1 | RPS6KB1 | RPTOR | RUNX1 | RUNX1T1 | RUNX3 | SDHA | SDHB |
SDHC | SDHD | SEMA3A | SEMA3E | SET | SETBP1 | SETD2 | SF3A1 | SF3B1 | SH2B3 | SKP2 | SLIT2 |
SMAD2 | SMAD3 | SMAD4 | SRSF2 | SRSF7 | STAG2 | STAT3 | STAT4 | TERT | TET2 | TP53 |
[DNA – Gene List]
ABL1 | ABL2 | ABRAXAS1 | ACVR1 | ACVR1B | ACVR2A | ADAM29 | ADGRA2 | ADTRP | AKT1 | AKT2 | AKT3 |
ALK | ALOX12B | ALOX15B | AMER1 | ANKRD11 | ANKRD26 | APC | APCDD1 | APEX1 | APOB | APOBEC1 | APOBEC3A |
APOBEC3B | AR | ARAF | ARFRP1 | ARID1A | ARID1B | ARID2 | ARID5B | ASTE1 | ASXL1 | ASXL2 | ATM |
ATP11B | ATR | ATRX | AURKA | AURKB | AXIN1 | AXIN2 | AXL | B2M | B3GAT1 | BACH1 | BAP1 |
BARD1 | BAX | BBC3 | BCL10 | BCL2 | BCL2A1 | BCL2L1 | BCL2L11 | BCL2L2 | BCL6 | BCL9 | BCOR |
BCORL1 | BCR | BEX5 | BIRC2 | BIRC3 | BLM | BMPR1A | BRAF | BRCA1 | BRCA2 | BRD2 | BRD3 |
BRD4 | BRIP1 | BTG1 | BTK | BTLA | CADM1 | CALR | CARD11 | CASP5 | CASP8 | CBFB | CBL |
CCDC150 | CCDC168 | CCDC43 | CCL2 | CCL4 | CCN6 | CCND1 | CCND2 | CCND3 | CCNE1 | CD27 | CD274 |
CD276 | CD28 | CD3D | CD3E | CD3G | CD4 | CD40 | CD44 | CD74 | CD79A | CD79B | CD8A |
CDC42 | CDC73 | CDH1 | CDH2 | CDH20 | CDH5 | CDK12 | CDK4 | CDK6 | CDK8 | CDKN1A | CDKN1B |
CDKN2A | CDKN2B | CDKN2C | CDX2 | CEBPA | CENPA | CHD1 | CHD2 | CHD4 | CHEK1 | CHEK2 | CHUK |
CIC | COLEC12 | COP1 | CRBN | CREBBP | CRK | CRKL | CRLF2 | CSF1R | CSF2 | CSF2RA | CSF2RB |
CSF3R | CSNK1A1 | CSNK2A1 | CTCF | CTLA4 | CTNNA1 | CTNNB1 | CUL3 | CUL4A | CUL4B | CUX1 | CXCL10 |
CXCL11 | CXCL9 | CXCR3 | CXCR4 | CYLD | CYP17A1 | CYP4Z2P | DAXX | DCUN1D1 | DDHD1 | DDR2 | DDX41 |
DEFB105A | DHX15 | DICER1 | DIS3 | DNAJB1 | DNMT1 | DNMT3A | DNMT3B | DOCK2 | DOCK3 | DOT1L | E2F3 |
EED | EGFL7 | EGFR | EIF1AX | EIF4A2 | EIF4E | ELMO1 | ELOC | EML4 | EMP1 | EMSY | EP300 |
EPCAM | EPHA3 | EPHA5 | EPHA6 | EPHA7 | EPHB1 | EPHB4 | EPHB6 | ERBB2 | ERBB3 | ERBB4 | ERCC1 |
ERCC2 | ERCC3 | ERCC4 | ERCC5 | ERG | ERRFI1 | ESR1 | ETS1 | ETV1 | ETV4 | ETV5 | ETV6 |
EWSR1 | EYA2 | EZH2 | FANCA | FANCC | FANCD2 | FANCE | FANCF | FANCG | FANCI | FANCL | FANCM |
FAS | FAT1 | FAT3 | FBXW7 | FGF1 | FGF10 | FGF12 | FGF14 | FGF19 | FGF2 | FGF23 | FGF3 |
FGF4 | FGF5 | FGF6 | FGF7 | FGF8 | FGF9 | FGFR1 | FGFR2 | FGFR3 | FGFR4 | FH | FLCN |
FLI1 | FLT1 | FLT3 | FLT4 | FOXA1 | FOXL2 | FOXO1 | FOXO3 | FOXP1 | FOXP3 | FRS2 | FUBP1 |
FYN | GABRA6 | GAS6 | GATA1 | GATA2 | GATA3 | GATA4 | GATA6 | GEN1 | GID4 | GLI1 | GNA11 |
GNA13 | GNAQ | GNAS | GPS2 | GREM1 | GRIN2A | GRM3 | GSK3B | GUCY1A2 | GZMA | GZMB | GZMH |
H1-2 | H2AC13 | H2BC5 | H3-3A | H3-3B | H3-4 | H3-5 | H3C1 | H3C11 | H3C12 | H3C13 | H3C14 |
H3C15 | H3C2 | H3C3 | H3C4 | H3C6 | H3C7 | H3C8 | HGF | HLA-A | HLA-B | HLA-C | HLA-DRA |
HLA-E | HLA-F | HLA-G | HNF1A | HNRNPK | HOXA3 | HOXB13 | HRAS | HSD3B1 | HSP90AA1 | ICOSLG | ID3 |
IDH1 | IDH2 | IDO1 | IDO2 | IFITM1 | IFITM3 | IFNA1 | IFNB1 | IFNG | IFNGR1 | IGF1 | IGF1R |
IGF2 | IGF2R | IKBKE | IKZF1 | IL10 | IL12A | IL12B | IL2 | IL23A | IL6 | IL7R | INHA |
INHBA | INPP4A | INPP4B | INSR | IRF2 | IRF4 | IRS1 | IRS2 | ITGAE | ITK | JAK1 | JAK2 |
JAK3 | JUN | KAT6A | KDM5A | KDM5C | KDM6A | KDR | KEAP1 | KEL | KIF5B | KIT | KLF4 |
KLHL6 | KMT2A | KMT2B | KMT2C | KMT2D | KNSTRN | KRAS | LAG3 | LAMP1 | LATS1 | LATS2 | LMO1 |
LRP1B | LRP6 | LTK | LTN1 | LYN | LZTR1 | MAGI2 | MAGOH | MALT1 | MAML1 | MAP2K1 | MAP2K2 |
MAP2K4 | MAP3K1 | MAP3K13 | MAP3K14 | MAP3K4 | MAPK1 | MAPK3 | MAX | MCL1 | MDC1 | MDM2 | MDM4 |
MED12 | MEF2B | MEF2C | MEN1 | MET | MGA | MITF | MLH1 | MLLT3 | MPL | MRE11 | MSH2 |
MSH3 | MSH6 | MST1 | MST1R | MTMR11 | MTOR | MTR | MUTYH | MYB | MYC | MYCL | MYCN |
MYD88 | MYL1 | MYLK | MYO18A | MYOD1 | NAB2 | NBN | NCOA3 | NCOR1 | NDUFC2 | NEGR1 | NF1 |
NF2 | NFE2L2 | NFKBIA | NKX2-1 | NKX2-8 | NKX3-1 | NOMO1 | NOTCH1 | NOTCH2 | NOTCH3 | NOTCH4 | NPM1 |
NRAS | NRG1 | NSD1 | NSD3 | NTRK1 | NTRK2 | NTRK3 | NUP93 | NUTM1 | PAK1 | PAK3 | PAK5 |
PALB2 | PARP1 | PARP2 | PARP3 | PARP4 | PAX3 | PAX5 | PAX7 | PAX8 | PBRM1 | PCDH17 | PDCD1 |
PDCD1LG2 | PDE4D | PDGFRA | PDGFRB | PDK1 | PDPK1 | PGR | PHF6 | PHLPP2 | PHOX2B | PIK3C2B | PIK3C2G |
PIK3C3 | PIK3CA | PIK3CB | PIK3CD | PIK3CG | PIK3R1 | PIK3R2 | PIK3R3 | PIM1 | PKHD1 | PLCG1 | PLCG2 |
PLK2 | PMAIP1 | PMS1 | PMS2 | PNP | PNRC1 | POLD1 | POLE | PPARG | PPM1D | PPP2R1A | PPP2R2A |
PPP6C | PRDM1 | PREX2 | PRF1 | PRKAR1A | PRKCI | PRKDC | PRKN | PRPF40B | PRSS8 | PTCH1 | PTCH2 |
PTEN | PTK2 | PTPN11 | PTPRC | PTPRD | PTPRS | PTPRT | PUS3 | QKI | RAB35 | RAC1 | RAC2 |
RAD17 | RAD21 | RAD50 | RAD51 | RAD51B | RAD51C | RAD51D | RAD52 | RAD54L | RAF1 | RANBP2 | RARA |
RASA1 | RB1 | RBM10 | RBMXL1 | RECQL4 | REL | RET | RFX1 | RHEB | RHOA | RHOB | RICTOR |
RIT1 | RNF19B | RNF43 | ROBO1 | ROBO2 | ROS1 | RPA1 | RPS6KA4 | RPS6KB1 | RPS6KB2 | RPTOR | RUNX1 |
RUNX1T1 | RUNX3 | RYBP | SDHA | SDHAF2 | SDHB | SDHC | SDHD | SEC31A | SEMA3A | SEMA3E | SET |
SETBP1 | SETD2 | SF3A1 | SF3B1 | SH2B3 | SH2D1A | SHQ1 | SKP2 | SLC22A9 | SLIT2 | SLITRK3 | SLX4 |
SMAD2 | SMAD3 | SMAD4 | SMAP1 | SMARCA1 | SMARCA4 | SMARCB1 | SMARCD1 | SMC1A | SMC3 | SMO | SNCAIP |
SOCS1 | SOX10 | SOX17 | SOX2 | SOX9 | SPEN | SPOP | SPTA1 | SRC | SRSF1 | SRSF2 | SRSF7 |
STAG1 | STAG2 | STAT3 | STAT4 | STAT5A | STAT5B | STC1 | STK11 | STK40 | SUFU | SUZ12 | SYK |
TACC3 | TAF1 | TBX22 | TBX3 | TCF3 | TCF7L2 | TENT5C | TERC | TERT | TET1 | TET2 | TFE3 |
TFRC | TGFBR1 | TGFBR2 | TIAF1 | TIGIT | TIPARP | TMEM127 | TMPRSS2 | TNF | TNFAIP3 | TNFRSF14 | TNFRSF18 |
TNFRSF4 | TNFSF13B | TNKS | TNKS2 | TOP1 | TOP2A | TP53 | TP63 | TRAF2 | TRAF7 | TRRAP | TSC1 |
TSC2 | TSHR | U2AF1 | U2AF2 | USP9X | VEGFA | VHL | VSIR | VTCN1 | WNT1 | WT1 | WWP1 |
XBP1 | XIAP | XPO1 | XRCC2 | XRCC3 | YAP1 | YES1 | ZBTB2 | ZBTB7A | ZFHX3 | ZNF217 | ZNF703 |
ZRSR2 |
[RNA – Gene List]
ABL1 | AKT3 | ALK | AR | AXL | BAIAP2L1 | BCL2 | BRAF | BRCA1 | BRCA2 | CCDC6 | CD74 |
CDK4 | CSF1R | EGFR | EML4 | ERBB2 | ERG | ESR1 | ETS1 | ETV1 | ETV4 | ETV5 | ETV6 |
EWSR1 | FGFR1 | FGFR2 | FGFR3 | FGFR4 | FLI1 | FLT1 | FLT3 | JAK2 | KDR | KIF5B | KIT |
KMT2A | LMNA | MET | MLLT3 | MSH2 | MYC | NCOA4 | NOTCH1 | NOTCH2 | NOTCH3 | NRG1 | NTRK1 |
NTRK2 | NTRK3 | PAX3 | PAX7 | PAX8 | PDGFRA | PDGFRB | PIK3CA | PPARG | RAF1 | RET | ROS1 |
RPS6KB1 | SEPTIN14 | SLC34A2 | SLC45A3 | TACC3 | TFG | TMPRSS2 | TPM3 |
암종과 연관 있는 것으로 알려진 유전자의 염기서열을 포괄적으로 분석하기 위한 패널. Immuno-oncology 마커를 비롯해 Gene Rearrangement 등 다양한 유전 변이를 분석하기 위한 패널
FDA 승인된 약물과 연관 있는 것으로 알려진 유전변이 검출을 위한 패널로 약물과 연관성이 높은 주요 유전자를 폭넓게 커버하는 패널
암종과 연관 있는 것으로 알려진 유전자의 염기서열을 포괄적으로 분석하기 위한 패널. Immuno-oncology 마커를 비롯해 Gene Rearrangement 등 다양한 유전 변이를 분석하기 위한 패널
유전성 암과 연관 있는 것으로 보고된 30여 개 유전자의 염기서열 분석을 위한 패널
FDA 승인된 약물과 연관 있는 것으로 알려진 유전변이 검출을 위한 패널로 약물과 연관성이 높은 주요 유전자를 폭넓게 커버하는 패널
셀레믹스에서 제공하는 BI 분석 서비스로 다양한 수준의 분석 결과 제공 가능
Technical Resources
[Product Sheet] Celemics CancerScreen Core/50/100/400
[Product Sheet] Celemics CancerScreen Comprehensive
[Product Sheet] Celemics CancerScreen Focus
[Product Sheet] Celemics CancerScreen CUP(Cancer of Unknown Primary)
Celemics Target Enrichment Panel Overview
Celemics Products & Services
Safety Data Sheets
최신 MSDS 파일이 필요하시면 ‘Contact Us‘를 통해 문의 주시기 바랍니다.
MSDS_CancerScreen Panels_Illumina
MSDS_CancerScreen Panels_Thermo Fisher
MSDS_CancerScreen Panels_MGI
Hwang J, Bang S, Choi MH, Hong SH, Kim SW, Lee HE, Yang JH, Park US, Choi YJ. Discovery and Validation of Survival-Specific Genes in Papillary Renal Cell Carcinoma Using a Customized Next-Generation Sequencing Gene Panel. Cancers. 2024 Jan;16(11):2006.
10.3390/cancers16112006
Ammous-Boukhris N, Abdelmaksoud-Dammak R, Ben Ayed-Guerfali D, Guidara S, Jallouli O, Kamoun H, Charfi Triki C, Mokdad-Gargouri R. Case report: Compound heterozygous variants detected by next-generation sequencing in a Tunisian child with ataxia-telangiectasia. Frontiers in Neurology. 2024 May 31;15:1344018.
10.3389/fneur.2024.1344018
Hwang J, Lee HE, Han JS, Choi MH, Hong SH, Kim SW, Yang JH, Park U, Jung ES, Choi YJ. Sex-specific survival gene mutations are discovered as clinical predictors of clear cell renal cell carcinoma. Scientific Reports. 2024 Jul 9;14(1):15800.
10.1038/s41598-024-66525-9