OncoScan™ CNV Reagent Kit for Research
FWS 제품은 특정 승인이 필요하므로 배송이 약 2-3주 더 소요됩니다.
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Applied Biosystems™

OncoScan™ CNV Reagent Kit for Research

The OncoScan CNV Reagent Kit is part of the OncoScan CNV Assay and so is used in conjunction with OncoScan자세히 알아보기
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카탈로그 번호수량
902692TS24 assays
카탈로그 번호 902692TS
제품 가격(KRW)
-
수량:
24 assays
The OncoScan CNV Reagent Kit is part of the OncoScan CNV Assay and so is used in conjunction with OncoScan CNV arrays. The OncoScan CNV Reagent Kit contains the copy number probe mix and controls, gap fill and 1st stage PCR reagents, 2nd stage PCR and post PCR processing reagents, stain reagents, and wash buffers.
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
용도(애플리케이션)CNV (Copy Number Variation)
유전형 분석 타겟Copy Number Variants
제품라인OncoScan
수량24 assays
샘플 종류DNA
유형CNV Reagent Kit
Unit SizeEach

자주 묻는 질문(FAQ)

Is there an equivalent metric for the "Offset Flag" in the QC and Sample Info tab in Chromosome Analysis Suite (ChAS) for OncoScan?

There is no available equivalent to the "Offset Flag" in the QC and Sample Info tab in ChAS. The "Offset Flag" is a QC metric that is found in the Analysis Dashboard for OncoScan products. This QC metric lets us know if the TuScan algorithm detected that the usual normalization method was off, and therefore required readjustment.

Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.

What data files are produced during the assay and analysis process?

These data files are produced that are key to the process:

ARR file - This file includes sample information.
AUDIT file - This file is a log of the sample history.
DAT file - This file is the raw data from the scanner.
CEL file - This file is the gridded and processed data.
xxCHP file - This file is the output of ChAS 3.1 and contains all of the analysis data.
CHPCAR file - This file stores user-annotated calls, interpretations, and modifications made to CHP file segment data (ChAS v2.0 and higher).

Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.

What is the difference between OncoScanCancerGeneOnly.r1 and OncoScanGeneBoundaries.r1?

OncoScanGeneBoundaries.r1 lists the approximately 900 OncoScan cancer genes and includes greater than 10 kb on each side of the gene. OncoScanCancerGeneOnly.r1 lists the same approximately 900 OncoScan cancer genes using the start and stop positions of the gene (no additional 10 kb on each side of the gene).

Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.

What does "low diploid flag" mean?

The algorithm identifies normal diploid markers in the cancer samples. This is particularly important in highly aberrant samples. The normal diploid markers are used to calibrate the signals so that a log2 ratio of 0 (e.g., copy number 2) is achieved. In about 2% of samples, the algorithm cannot identify a sufficient number of “normal diploid” markers, and no normal diploid calibration occurs. This event triggers “low diploid flag = YES.” In this case, the user needs to carefully examine the log2 ratios and verify that re-centering is necessary.

Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.

What is "celpaircheckstatus," and what does it do?

Celpaircheckstatus checks if the results from the AT channel are consistent with the results from the GC channel and represent the results of the respective channel. This metric will be “out of bounds,” for example, when the AT and GC channels were mispaired between samples or due to sample contamination. We recommend troubleshooting as described in the OncoScan Console User Manual.

Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.