- Array Designer
- Array Designer是一个独特DNA微矩阵(microarray)软件,批量设计DNA和寡核苷酸引物工具,可用来设计出高精准的寡核苷酸和基因显现,SNP基因分析,微阵列实验所需的引物。只按下几个按钮就能设计出CDNA的引物和寡核苷酸微阵列。该软件是一个独特的微阵列软件,可用来设计出高精准的寡核苷酸和基因显现,SNP基因分析微阵列实验所需的引物。
- Windows;Linux
- 加拿大
- 英文
- 电话:021-64391516,传真:021-64391506

-
- Primer Premier (专业的引物设计软件)
- Primer Premier是大名顶顶的PREMIER公司出品的引物设计软件,用来帮助研究人员设计最适合引物的应用软件利用它的高级引物搜索引物数据库巢式引物设计引物编辑和分析等功能可以设计出有高效扩增能力的理想引物也可以设计出用于扩增长达50kb以上的PCR产物的引物序列,由加拿大的Premier公司开发的专业用于PCR或测序引物以及杂交探针的设计,评估的软件,和Plasmid Premier2.0...

-
- Xpression Primer (专业的实时定量PCR引物和探针设计软件)
- Xpression Primer 实时定量PCR引物和探针设计的专用软件。运用成熟的基因算法来设计优化标记引物来扩大对克隆系统的基因表达的ORFs。这款软件非常灵活,它能够与研究者任何真实选择的表达系统兼容。Xpression Primer也可以设计优化序列引物(sequencing primers)来修正转录。

-
- TMA Foresight (功能强大组织芯片数据分析的工具)
- TMA Foresight 是一款功能强大组织芯片数据分析的工具,进行多元统计技术如用Cox危险的预兆特点、等级分布和最后存活点的比例模型来探讨关联的表达和预测的临床病理变数与结果。由于TMA Foresight 不仅能够分析数据而且能够解释数据,所以它对病理、临床和研究都是非常有用的工具。

-
- SimVector (专业的DNA和质粒图分析软件)
- SimVector(DNA分析和质粒图)一款为绘制高质量的适合发表的矢量图和设计克隆试验的工具。能自动生成发表质量的载体图谱帮助克隆实验设计分析。它能自动设计TA和限制性酶等克隆方法的实验方案。此外,也可以输出传统的位图格式和网页的格式。正因为它具有如此强大的绘图特点,图谱可以附带各种图样风格线条和色彩和注解等。具有全面的项目管理功能,用于序列分组和系统化存...

-
- SimGlycan (专业的多糖结构预测分析软件)
- SimGlycan能从质谱分析中获得的数据预测多糖的结构,应用于生物化学的专业软件。SimGlycan预测聚糖的结构,通过由质谱测定法得来的MS/MS数据,更方便于做糖基化和后修饰研究。SimGlycan接受由质谱仪产生得试验性MS文件,将它们同其自己超过7000个聚糖的理论分段比较,并产生可能的聚糖结构清单。每个结构被记分以反应它们如何匹配实验数据。而其他可能的聚糖的生物信息诸如...

-
- PrimerPlex (Oligo Design for High Throughput SNP Genotyping, SNP Analysis & More...)
- A unique tool developed for designing oligos for direct hybridization and Allele Specific Primer Extension (ASPE) assays for multiplex systems based on Luminex's xMAP® technology.

-
- Beacon Designer (专业的实时多元反应测试软件)
- Beacon Designer是专业的实时荧光定量PCR分子信标(Molecular beacon )及TaqMan探针设计软件,通过该软件,你可以设计内嵌染料探针,TaqMan荧光探针,FRET荧光探针和分子信标探针来测试PCR产品的实时多元反应。

-
- AlleleID (专业的生物检测软件)
- AlleleID是一款专业的生物检测软件。通过排列次序定位DNA的差异位点,并查找蛋白质组间氨基酸的区域,专门为检测研究病原体,细菌鉴定、物种鉴定以及生物门类辨识 提供微阵列(MICROARRAY)和定量聚合酶链反应(qPCR)试验而设计。
Array Designer是一个独特DNA微矩阵(microarray)软件,批量设计DNA和寡核苷酸引物工具,可用来设计出高精准的寡核苷酸和基因显现,SNP基因分析,微阵列实验所需的引物。只按下几个按钮就能设计出CDNA的引物和寡核苷酸微阵列。该软件是一个独特的微阵列软件,可用来设计出高精准的寡核苷酸和基因显现,SNP基因分析微阵列实验所需的引物。
Oligo & cDNA Microarray Design Software
Array Designer designs thousands of primers and probes for oligo and cDNA microarrays in seconds. It designs probes for SNP detection, microarray gene expression and gene expression profiling. In addition, comprehensive support for tiling arrays and resequencing arrays is available.
BLAST Search for Specific Design
Array Designer designs highly specific oligos by interpreting the results of a BLAST search performed against any genomic database available at NCBI or a local custom database. Any significant homologies identified are automatically avoided while designing oligos. Repeat regions are identified and automatically avoided.
Standard Array Design: You can design primers and probes for SNP detection and gene expression profiling on multiple sequences in a single search run. Our customers, typically choose over 10,000 sequences at a time.
Whole Genome Array: With Array Designer you can study the genetic make-up of entire organisms effortlessly by detecting every gene or exon in the whole genome. This enables easy discovery of differentially and alternatively spliced transcripts, SNPs, DNA sequence variation in individuals or populations and comparative genome hybridization (CGH).
Tiling Arrays: You can spot every base of a long genomic sequence also known as whole genome amplification, avoiding repetitive regions. Designing arrays to characterize regulatory elements, or to study epigenetic modifications, methylation patterns and protein binding sites has never been so easy.
Resequencing Arrays: Array Designer designs resequencing arrays with which you can detect SNP and other sequence variations in a large number of samples. One of the common problems in resequencing array design is false base calls caused by inter-template cross hybridization. With the unique feature which we call project BLAST, you can identify and avoid the homologous regions that create false positives.
Microarray Gene Expression
Probe and primer design
Choices in probe design: Array Designer can design single or multiple probes per sequence for your microarray projects. Allows specifying the minimum distance between two probes to avoid overlapping.
Product Location: Allows specifying the product (amplicon) length and product location viz at the 3’end, 5’end or anywhere in the sequence.
Comprehensive selection criteria: Screens oligos for their thermodynamic properties as well as secondary structures. Graphics for the structures are also displayed.
Ranking: Uses statistical optimization techniques to design the best primer and probe for each template. A list of alternate designs is also available.
Algorithm: Calculates oligo Tm using nearest neighbor thermodynamic algorithm.
BLAST search
Specificity Check: Thousands of searches are submitted automatically. Results are interpreted and displayed in the Homology Avoidance window.
Batch Sequence BLAST search: Array Designer can BLAST search hundreds of sequences. The results are interpreted and the homologies identified are avoided while designing primers.
Local BLAST: Array Designer can BLAST search against a custom local database that can be set up on a Unix machine using the WWW Standalone BLAST facility of the NCBI. Read the inbuilt product help for details.
Desktop BLAST: BLAST search sequences against local custom databases without the need of setting up a server on a separate machine. Simply save the sequence files (.txt or .fa) on your computer and ask Array Designer to BLAST search your query sequence against them.
Verification of specific design: The primers and probes designed by the program can be BLAST searched against all the nucleotide databases available at NCBI to verify the specificity of design.
Repeat regions: Optimizes BLAST search parameters to detect human repeats while searching the human RNA (previously called mRNA) database at NCBI.
SNP detection & SNP genotyping
SNP loading: Easily add a single SNP at a time or load thousands of SNPs using standard GenBank variation files.
SNP Detection: Designs probes for SNP detection (both wild and mutant) with SNP at the center of the probe.
SNP genotyping with Array Designer: Designs SNP genotyping probes with SNP or one base upstream of the 3' end of the probe.
Whole genome array
By length: Probes can be designed for the fragments of a size chosen by the user. The sequence is broken down into small equal-sized fragments and then a specific probe is designed for each one of them.
By position: Probes can be designed on genes/fragments, the start and stop position for which can be imported from a text file.
By annotation: Probes can be designed on genes or exons, the annotations for which can be read from the GenBank file.
BLAST to ensure specificity: For a whole genome sequence, Array Designer automatically creates a local custom database of the input sequence and BLAST searches every fragment against it. To verify the specificity of design, you can BLAST the designed oligos.
Sequence size: Array Designer can design probes spanning the entire genome of the organism. This ability is especially useful to study the expression of intergenic and intragenic regions. Fragments to be studied can be generated on the basis of their length, their position or by specifying an annotation such as gene, exon or both.
Uniform Tm values: Array Designer designs probes free of secondary structures and with uniform Tm values ensuring a high rate of success of microarray experiments.
Tiling arrays
Sequence size: Array Designer can design tiling primers to study protein binding regions of small to medium sized genomes. You can generate both distinct or overlapping amplicons depending on the specificity desired.
Distinct amplicon: Primers are designed such that there is no overlap between adjacent amplicons.
Overlapping amplicon: Primers are designed such that the adjacent amplicons overlap each other in the flanking regions.
Whole Genome Amplification using Array Designer
Resequencing arrays
Resequencing probe design: In addition to standard probes, Array Designer also designs resequencing arrays. With custom resequencing arrays, you can detect SNP and other sequence variations in a large number of samples for applications such as biowarfare pathogen studies, bacterial identification, predisposition and resistance to disease or discovering the genetic basis of phenotypic traits.
BLAST search: The challenge in designing chips for resequencing by hybridization is to achieve the lowest possible false positive rate. Array Designer offers an innovative and unique project BLAST capability to identify these regions and recommends a multi-chip solution.
Avoiding repetitive regions: You can simply connect to the popular Repeat Masker using the handy link and Array Designer will avoid creating spots that may generate false positives.
CnSciTech