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The AmoyDx® HANDLE HRR NGS Panel facilitates the detection of somatic and germline variants across 27 genes within the Homologous Recombination Repair (HRR) pathway, along with 5 tumor driver genes.





 

Mutations( Hover over each mutational type to highlight genes covered )

All
LR
SNV/INDELS
BRCA1

BRCA1

LR
SNV/INDELS
BRCA2

BRCA2

LR
SNV/INDELS
AR

AR

SNV/INDELS
ATM

ATM

SNV/INDELS
ATR

ATR

SNV/INDELS
BARD1

BARD1

SNV/INDELS
BRIP1

BRIP1

SNV/INDELS
CDH1

CDH1

SNV/INDELS
CDK12

CDK12

SNV/INDELS
CHEK1

CHEK1

SNV/INDELS
CHEK2

CHEK2

SNV/INDELS
ESR1

ESR1

SNV/INDELS
FANCA

FANCA

SNV/INDELS
FANCL

FANCL

SNV/INDELS
HDAC2

HDAC2

SNV/INDELS
HOXB13

HOXB13

SNV/INDELS
MRE11

MRE11

SNV/INDELS
NBN

NBN

SNV/INDELS
PALB2

PALB2

SNV/INDELS
PPP2R2A

PPP2R2A

SNV/INDELS
PTEN

PTEN

SNV/INDELS
RAD51B

RAD51B

SNV/INDELS
RAD51C

RAD51C

SNV/INDELS
RAD51D

RAD51D

SNV/INDELS
RAD54L

RAD54L

SNV/INDELS
STK11

STK11

SNV/INDELS
TP53

TP53

SNV/INDELS
BRAF

BRAF

SNV/INDELS
ERBB2

ERBB2

SNV/INDELS
KRAS

KRAS

SNV/INDELS
NRAS

NRAS

SNV/INDELS
PIK3CA

PIK3CA

SNV/INDELS

Secure data analysis and interpretation

Secure data analysis and interpretation

Detection of SNVs, InDels and LRs

Detection of SNVs, InDels and LRs

Fast turnaround time and cost-effective

Fast turnaround time and cost-effective

Streamlined one-tube workflow

Streamlined one-tube workflow

Specifications

Alterations detected
SNV, Indel (somatic/germline), LR (germline for BRCA1/2)
Sample type
Fresh-frozen/FFPE tissue, whole blood
Sequencer
Illumina NovaSeq 6000, NextSeq 500, MiSeq, MiSeqDx, MiniSeq, iSeq 100, Salus Pro
TAT for library preparation
5 hours (hands-on time < 1 hour)
TAT from sample to report
3 days

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