Thermo Fisher Scientific Variant Reporter Software v1.0
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
4440846 | - | Thermo Fisher Scientific 4440846 Variant Reporter Software v1.0 1 software pk | 재고문의 | pk | 0원 | - | 0원 |
다른 상품 둘러보기
Applied Biosystems™
Variant Reporter™ Software v1.0
The Variant Reporter™ Software performs comparative sequencing, also known as direct sequencing, medical sequencing, PCR sequencing and resequencing with DNA자세히 알아보기
The Variant Reporter™ Software performs comparative sequencing, also known as direct sequencing, medical sequencing, PCR sequencing and resequencing with DNA sequencing files. The software is designed for reference based and non-reference based analysis such as mutation detection and analysis, SNP discovery and validation and sequence confirmation. The robust algorithms will call SNPs, mutations, insertions, deletion and heterozygous insertions⁄deletions for data generated using the Applied Biosystems Genetic Analyzers.
• Handle greater that 10 times more sample files than competing software products
• Reduce labor and project cost with accelerated data review
• Improve your results with fast, accurate heterozygote calling
• Simple to learn – requires less than one hour
• Robust data filtering with new more effective quality metrics
Save Time
Manually reviewing your resequencing results requires valuable time and reduces productivity. Variant Reporter™ Software v1.0 does it all for you, quickly, efficiently, and accurately. Designed for basic and clinical researchers engaged in genotyping projects, as well as core resequencing labs whose focus is secondary analysis, this new variant detection software solves the workflow bottleneck caused by the 3–8 hours often required by other software products for data analysis and review. And with your resequencing workflow fully automated, you are free to concentrate on other aspects of your project.
Simple Workflow
To set up a project, simply import and group traces into amplicons and specimens. The analysis parameters can be adjusted and a reference defined, although the data can be analyzed with or without a reference. The software automatically groups traces into specimens and amplicons based on sample file name parsing. Next, analyze your project. After analyzing the data, the software calculates the project-quality statistics and generates an overview of the project data quality. If samples pass QC thresholds, the software will skip this step. Users can also drill down to review the quality of specimens, amplicons, or individual traces. The software contains all the viewing and reporting functionalities of Sequence Scanner Software.
A Choice of Reports
Users can select from the following reports and exports:
• Project Summary Report: Contains high-level project statistics, lists of variants and genotypes, and snippets of each variant
• Quality Report: Provides a comprehensive view of trace, specimen, amplicons, and project quality
• Specimen Report: For clinical researchers interested in reporting data one subject at a time, this report provides specimen statistics, specimen genotypes, and snippets of each variant for one or all specimens in a project.
Use in Resequencing Applications
Resequencing – also known as comparative, direct, medical, or PCR sequencing – is useful for discovering variants, including HIMs, insertions, deletions, SNPs, and genotypes. The process begins when a researcher chooses a gene of interest, isolates DNA from the gene, amplifies one or more amplicons for each exon, and then performs cycle sequencing using the BigDye™ Terminator Cycle Sequencing Kit, followed by cleanup with the BigDye™ XTerminator™ Purification Kit. The sample is then run on an Applied Biosystems capillary electrophoresis instrument. During the final step, Variant Reporter Software discovers the variants, determines the genotypes, and creates a report. That`s all there is to it.
For Research Use Only. Not for use in diagnostics procedures.
사양
제품라인Variant Reporter™
Software TypeVariant Reporter™ Software, Comparative Sequencing
데이터 입력Sequencing traces
데이터 출력Variant Reports with sequence comparison metrics
용도(장비)310 Genetic Analyzer, 3130xl Genetic Analyzer, 3730xl DNA Analyzer, 3730 DNA Analyzer
라이선스Static
운영 체제Windows Vista, Windows XP, Windows Vista Business, Windows 2000 (Service Pack 4), Windows XP (Service Pack 2), Windows 2000
제품 유형Variant Reporter Software V1.0
수량1 software
소프트웨어 카테고리Software
Unit Size1 software
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